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  • 1990-1994  (725)
  • 1920-1924  (750)
  • 1994  (725)
  • 1924  (750)
  • Inorganic Chemistry  (1,438)
  • crystal structure  (154)
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  • 1990-1994  (725)
  • 1920-1924  (750)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Il nuovo cimento della Società Italiana di Fisica 16 (1994), S. 1671-1678 
    ISSN: 0392-6737
    Keywords: Effects of material synthesis ; crystal structure ; chemical composition ; Y-based compounds ; Conference proceedings
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Summary YBCO with high granulometric perfection and low dispersion can be obtained by a low-temperature reaction (≈800°C) of atomic-scale dispersed powders, produced through the thermal decomposition of liquid precursors. As reacted such powders are tetragonal and not superconducting, but they transform into the high-T c phase after optimized annealing treatments. We describe the method we developed and the characteristics of the materials we achieved, and we discuss the main features of the process in the light of the current know-how.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 24 (1994), S. 759-762 
    ISSN: 1572-8854
    Keywords: Sulfonamide ; methanesulfonanilide ; crystal structure ; molecular structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound, crystallizes in the triclinic space group $$P\bar 1$$ witha=8.232(4),b=9.159(2),c=10.230(3)Å. α=74.07(3)°, β=72.50(4)°, γ=63.65(3)° andZ=2. The structure was solved by direct methods and refined by full matrix least squares methods toR=0.054 for 1817 observed reflections. The plane containing the nitrogen and sulfur atoms is perpendicular to the aromatic plane. One of the S−O bonds in each methanesulfonyl group is in nearly eclipsed conformation with the N−C bond.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 24 (1994), S. 437-440 
    ISSN: 1572-8854
    Keywords: Ca(C4H4O4)·H2O ; pentagonal pyramid ; calcium succinate ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The crystal structure of calcium succinate monohydrate, Ca(C4H4O4)·H2O, has been determined by single crystal X-ray diffraction. The crystals are monoclinic witha=11.952(2),b=9.691(2),c=11.606(2)Å, β=108.81(1)°, space group C2/c,Z=8,V=1272.49 Å3,d m =1.80, andd c =1.818 Mg m−3. The structure was refined by full-matrix least-squares techniques toR=0.027,R w =0.040, for 829 reflections with1≥3δ(I). Ca is coordinated to seven oxygen atoms, and the coordination polyhedron is best described as a pentagonal bipyramid. One carboxylate group in the succinate ion is bonded to three different Ca ions, forming a four-membered chelate ring with one Ca ion is bonded to three different Ca ions, forming a four-membered chelate ring with one Ca ion and unidentate bridge bonds to two other Ca ions. The other carboxylate group is bonded to two Ca ions through unidentate bonds. The structure is highly polymeric. The general structural features are nearly identical to those of calcium adipate monohydrate.
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  • 4
    ISSN: 1572-8854
    Keywords: Pyrimidine ; uracil ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract A new and easy method for the preparation of 1,3,7,9-tetramethylpyrido-[2,3-d∶6,5-d′]-dipyrimidine-2,4,6,8-tetrone is described. The structure of this compound has been solved by means of X-ray diffraction methods. The chemical characterization by spectral (mass, ultraviolet, infrared, and proton nuclear magnetic resonance) and thermal (thermogravimetry and differential scanning calorimetry) method is also reported. The compound is monoclinic, space groupP21/c,a=12.720(5),b=13.688(7),c=8.079(2) Å, β=107.06(4)°,Z=4. The structure consists of discrete tricyclic molecules, stacking playing an important role in crystal packing.
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  • 5
    ISSN: 1572-8862
    Keywords: Tungsten ; isomeric forms ; crystal structure ; triple bonds ; interconversion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract A thorough study of compounds with the formula W2Cl4(NHCMe3)2(PR3)2, withR 3=Me3, Et3, Prg n 3 Me2,Ph, is reported. In addition to the previously reported crystalline compounds, namely Ia,trans-W2Cl4(NHCMe3)2(PMe3)2 in space group Pmmn;3a,trans-W2Cl4(NHCM3)2(PEt3)2 in space group P21/a (or P21/c); and4,cis-W2Cl4(NHCMe3)2(PMe2Ph)2 in Pna21, we have obtained and structurally characterized the following new substances,1b,trans-W2Cl4,(NHCMe3)2(PMe2)2, space group P21/c,a= 12.233 (4) Å,b= 12.872 (4) Å,c=17.095 (5) Å,β=93.52 (2)°,Z=4,V=2687 (1) Å3 2,cis-W2Cl4(NHCMe3)2(PMe3)2, P21/c,a=9.673 (4) Å,b=17.249 (4) Å,c=16.244 (5) Å,β=99.63 (3),Z = 4 ,V=2669 (1) Å.3b,trans-W2Cl4(NHCMe3)2(PEt3)2, Pl,a=16.850 (3) Å,b=17.797 (3) Å,c= 11.459 (2)Å,α= 101.02 (1),β= 103.13°, y=84.23 (1)°,Z=4,V= 3279 (1) Å5,trans-W2Cl4(NHCM3)2(PMe2Ph)2, Fdd2,a=39.563 (8) Å at 20°C; 39.325 (10) Å at -6O°C,b = 57.543 (17) Å at 20°C; 57.186 (16) Å at -60°C,c= 8.810 (1) Å at 20°C; 8.770 (1) Å at - 60°C ,Z=24,V=20057 (7) Å3 (20°C), 19723 (8) Å3 ( - 60°C) .6,trans-W2Cl4(NHCMe3 2(PPrn 3)2, Pl,a= 17.287 (2) Å (20°C); 17.077 (5) Å (-60°C),b= 19.119 (2) Å (20°C); 18.952 (6) Å (-60°C),c= 12.713 (1) Å (20°C); 12.668 (4) Å (-60°C),Z=4,V= 3980 (1) Å3 (20°C), 3898 (2) ,Å3 ( - 60°C). In addition, the structure of3a was re-determined and refined so that the disorder ratio was a refined parameter, leading to a value of 0.520:0.480 instead of being arbitrarily fixed at 0.50:0.50. In all of the structures the molecules are held in eclipsed (but very distorted) rotational conformations and the W-W distances are all within the range of 2.305-2.330 Å. As will be shown in a later paper, for all phosphines, thecis andtrans isomers are of similar stability and an equilibrium mixture exists in solution. It is also shown that1a and3a do not contain unexpectedly short W-N bonds as previously reported.
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  • 6
    ISSN: 1572-8862
    Keywords: Mixed metal cluster ; alkyne ; diphenylacetylene ; platinum ; osmium ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract The new platinum-osmium alkyne cluster complex Pt2Os4(CO)8(μ3-PhC2Ph)3 (μ 4-PhC2Ph),2, was obtained from the reaction of Pt2Os4(CO)18,1b, with PhC2Ph and was characterized by IR.1H NMR and single-crystal X-ray diffraction analyses. The cluster of compound2 consists of an osmium capped Pt2Os3 square pyramid. It aLso contains three triply bridging and one quadruply bridging diphenylacetylene ligands. Crystal data for2: space group PI,a = 12.530(2) Å,b = 21.565(4) Å,c = 11.284(2) Å,α = 100.31(2),β = 111.89(1),β = 76.78(2),Z = 2, 3879 reflections,R = 0.032.
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  • 7
    ISSN: 1572-8854
    Keywords: Centrosymmetric ; symmetry ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound crystallizes in the centrosymmetric triclinic space group $$P\bar 1$$ (C 1 l ; No.2) witha=9.9143(10) Å,b=10.2616(11) Å,c=10.7715(10) Å, α=113.887(8)°, β=109.197(8)°, γ=90.699(9)°,V=932.78(17) Å3 andZ=1. A total of 4869 data were collected and merged to a set of 2450 independent reflections; the structure was solved and refined toR=1.42% andwR=1.94%. The molecule lies on a site of $$\bar 1$$ symmetry and is disordered, with obvious scrambling of carbonyl and chloride ligands. Resulting bond lengths include Ir−P=2.339(1) Å, Ir−Cl=2.398(4) Å and Ir−CO=1.808(15) Å.
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  • 8
    ISSN: 1572-9605
    Keywords: High-Tc superconductivity ; La1.9Bi0.1CuO4+δ ; excess oxygen ; crystal structure ; superconducting transition temperature
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: Abstract We have investigated the relation between the crystal structure and superconductivity in La1.9Bi0.1CuO4+δ , in which the phase separation observed in La2CuO4+δ is suppressed. A phase diagram in theT−δ plane is given for La1.9Bi0.1CuO4+δ with excess oxygen. For very smallδ values, the crystal structure is orthorhombic, and an orthorhombic-tetragonal phase transition occurs markedly atδ ∼ 0.03 in the measured temperature range between 13 and 293 K. Superconductivity is observed in the range of 0.04〈δ〈0.11. This is clear evidence thathigh-T c superconductivity also appears in the tetragonal phase.
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  • 9
    ISSN: 1572-882X
    Keywords: cellulose I ; molecular mechanics ; crystal structure ; molecular ; modelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Energies for various trial packing arrangements of unit cells for the Iα and Iβ phases of native cellulose discovered by Sugiyamaet al. were evaluated. Both a rigid-ring method, PLMR, and the full-optimization, molecular mechanics program, MM3(90), were used. For both phases the models that had the lowest PLMR energy also had the lowest MM3 energy. Both calculated models have the chains packed ‘up’, O6s intg positions, and the same sheets of hydrogen-bonded chains. The Iβ structure model is essentially identical to that proposed previously for ramie cellulose by Woodcock and Sarko. It is also the same as the best parallel model previously proposed that was based on the X-ray data of Mann, Gonzalez and Wellard, once the various unit cell conventions are considered. Also, the energies from both methods for all three celluloses, Iα, Iβ and II, are in the order that rationalizes their relative stabilites.
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  • 10
    ISSN: 1573-904X
    Keywords: ephedrine ; pseudoephedrine ; salicylate ; chirality ; salt formation ; homochiral crystal ; racemic compound ; racemic conglomerate ; crystal structure ; conformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The physicochemical properties and crystal structures of the crystalline salts formed by the interaction of an achiral anion, salicylate, with homochiral and racemic ephedrinium and pseudoephedrinium cations were determined. The interaction of ephedrinium or pseudoephedrinium with salicylate in aqueous solution yielded crystalline salts with the notable exception of homochiral ephedrinium. Evaporation of the solvent from solutions of homochiral ephedrine and salicyclic acid in various organic solvents, as well as grinding together solid homochiral ephedrine and solid salicylic acid, yielded viscous semisolids suggesting that homochiral ephedrinium salicylate has a low melting point and/or a high aqueous solubility. Mixing of the two viscous solids, obtained by grinding each of the opposite enantiomers of ephedrine with equimolar salicylic acid, resulted in the formation of racemic ephedrine and subsequently, upon heating, in the formation of racemic ephedrinium salicylate. While racemic ephedrinium salicylate exists as a crystalline compound (P21/n space group) with an equal number of opposite enantiomers in the unit cell, its diastereomer, racemic pseudoephedrinium salicylate, exists as a conglomerate, i.e. a physical mixture, of the homochiral crystals of the opposite enantiomers (each P21 space group). The inability of homochiral ephedrinium to exist as a crystalline salicylate salt at 20–25°C is attributed to its high energy conformation and/or to the poor packing of homochiral ephedrinium salicylate molecules in the crystal lattice.
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  • 11
    ISSN: 1572-9001
    Keywords: tris(pyrazol-1-yl)-s-triazine ; crystal structure ; electron diffraction ; AM1 semiempirical calculation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The conformation of the TPT molecule has been analyzed using experimental and computational techniques. The solid-state molecular structure shows similar conformational features to those in the 2-pyrimidine and phenyl derivatives although a different pattern of bond angles in the triazine ring was observed. The AM1 calculations predicted two conformations of comparable stability (ΔE=1.8 kcal/mol) differing in the orientation of one pyrazole ring. While the minimum energy conformation corresponds to a model displayingC 3h symmetry (φ 1=φ 2=φ 3=0°), the other minimum (φ 1=φ 2=0°,φ 3=180°) is close to that observed in the solid state. The electron diffraction results are consistent with a planar or nearly planar conformation in agreement with the preceding studies.
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  • 12
    ISSN: 1572-9001
    Keywords: Isocinchomeronic acid ; 2,5-pyridinedicarboxylic acid ; hydrogen isocinchomeronate ; manganese(II) complex ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The reactions between Mn(II), Co(II), Ni(II), and Zn(II) ions with isocinchomeronic acid (H2-isocin) afforded complexes of the general formula M(H-isocin)2-2H2O, whereas Fe(II) gives both red and deep red-brown products of the same formula. Various physical measurements suggest that the complexes of M = Co, Ni, Zn, and Fe (brown) are octahedrally coordinated by two aqua ligands and twotrans-N,O-bidentate H-isocin− anions with dimeric hydrogen bonding. Those for M = Mn and Fe (red) are the correspondingcis isomers. The structure of the manganese complex as determined by X-ray crystallography exhibitsC 2 molecular symmetry with Mn-N = 2.279(2), Mn-O(H-isocin)− = 2.196(2), and Mn-O(aqua) = 2.137(2) Å. Each aqua ligand forms two donor O-H ⋯ O hydrogen bonds with carboxy groups of different molecules in adjacent chains.
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 24 (1994), S. 731-737 
    ISSN: 1572-8854
    Keywords: Synthesis ; crystal structure ; IR data
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The synthesis, crystal structure and IR data are reported for Na2[Zn(CMA)4]·2EtOH·7H2O, where CMA− is the 9,10-dihydro-9-oxo-10-acridinacetate ion. The complex crystallizes in the monoclinic space group P2/n, with cell dimensionsa=17.335(9),b=8.440(5),c=21.875(12) Å, β=91.94(5)°,Z=2. The structure was solved by direct methods and refined to a finalR value of 0.0363 for 3022 non-zero reflections. The Zn2+ ion occupies twofold axis and is coordinated to four carboxylate ligands, the ZnO4 tetrahedron is considerably distorted with Zn−O distances of 1.978(3) and 1.961(3)Å. Each Na+ cation interacts with two water, one ethanol, and three carboxylate O atoms comprising distorted octahedron. The Zn2+ and Na+ cations are linked through monooxygen and syn-syn carboxylate bridges forming a trinuclear, mixed-metal cluster. The Zn...Na separation is 3.267(2)Å and Na...Na distance equals 3.520(2)Å. All oxygen bonded H-atoms are utilized in hydrogen bonds. The acridone rings overlap in the crystal with the 3.5 Å interlayer separations. The compound has been characterized by IR spectroscopy.
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  • 14
    ISSN: 1572-8862
    Keywords: Mixed metal ; platinum ; ruthenium ; alkyne ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstarct The ten metal cluster complex Pt2Ru8(CO)23(µ3−H)2, 1 was found to react with EtC2Et to form a new ten metal tris-alkyne complex Pt2Ru8(CO)18(µ3−EtC2Et)2 (µ4−EtC2Et),2 in 35% yield. Complex 2 was characterized by IR,1H NMR , and single crystalx-ray diffraction analyses. The cluster can be viewed as a dodecahedron of eight metal atoms capped with two ruthenium carbonyl groups, two triply bridging EtC2Et ligands and one quadruply bridging EtC2Et ligand. Application of the standard electron counting procedures indicate that this is an unusual complex in which the 18 electron rule applies and the polyhedral skeletal electron pair theory does not. Crystal Data for 2 2.0.5 CH2CI2: space group = P21,a = 12.759(2) A,b=18.438(2)Å,c = 20.197(3) Å,β = 91.59(1)°, Z. = 4, 6394 reflections,R = 0.037.
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  • 15
    ISSN: 1573-1111
    Keywords: 12-Membered crown ethers ; ion-selective membrane electrodes ; complexes ; crystal structure ; X-ray analysis ; conformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Lipophilic derivatives of benzo-12-crown-4 and naphtho-12-crown-4 have been synthesized. The behavior of the parent compounds and their derivatives in membrane ion-selective electrodes have been studied. Selectivity changes have been observed with the rise in lipophilicity. Crystal structures of the NaI and KI complexes of benzo-12-crown-4 (1 and2) have been determined by X-ray analysis. The alkali metal and iodide ions are in direct contact in2 but not in1. Compound1 [Na(benzo-12-crown-4)2]·I is triclinic, witha=13.368(8),b=10.727(7),c=10.325(4) Å; α=73.56(4),β=77.73(4), γ=108.70(5)°;Z=2, space group is $$P\bar 1$$ . Compound2 [K(benzo-12-crown-4)2·I] is monoclinic, witha=15.807(8),b=12.043(4),c=15.601(6) Å,β=117.74(3)°;Z=4, space groupC2/c. In both compounds the cations interact with all oxygen atoms of two crown ether molecules. Correlation of the crystal structures and behavior of the crown ethers in ion-selective membrane electrodes is discussed.
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 20 (1994), S. 53-71 
    ISSN: 1573-1111
    Keywords: Lithium ionophores ; podand ; dicyclohexylamides ; Li-complex ; crystal structure ; X-ray analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The influence of structure and lipophilicity of dicyclohexylamides on the lithium selectivity in membrane electrodes is discussed. The crystal structures of the triamide podand1 and its complex with LiBr1b has been determined by X-ray analysis. Crystal data for ligand1: C48H83O6N3, triclinic,P1,a=10.749(2),b=12.097(3),c=19.123(6)Å, α=95.76(2),β=80.06(2), γ=100.27(2)0,V=2403(1) Ã3,Z=2. Crystal data for the lithium complex1b: C48H83O6N3·LiBr·x C2H5OH, monoclinic,P2 1/c,a=21.297(6),b=16.316(8),c=19.450(4) Å,β=110.87(2)0,V=6315(3) Å3,Z=4. In the complex the ligand adopts a conformation in which oxygen binding sites surrounding the Li+ cation form a slightly distorted trigonal prism.
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 17 (1994), S. 137-148 
    ISSN: 1573-1111
    Keywords: Clathrate hydrate ; phase diagram ; crystal structure ; tetraisoamylammonium fluoride
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The phase diagram of the binary (i-C5H11)4NF-water system has been studied in the clathrate formation region. Three polyhydrates have been discovered, two of which (1∶38.9 and 1∶32.7) are the known orthorhombic and tetragonal phases:Pbmn,a=11.88,b=21.53,c=12.70 Å,ρ means=1.019 g cm-3 (0°C), m.p.=32.4°C andP42/m, a=23.729,c=12.466 Å,ρ means=1.062 g cm-3, (0°C), m.p.=31.2°C, respectively. A single crystal X-ray analysis of the novel clathrate hydrate (i-C5H11)4NF·27 H2O is reported. This new clathrate hydrate is tetragonal,I4I/a, witha=16.894(5),c=17.111(2) Å,Z=4, (−50°C), and m.p.=34.6°C. Each (i-C5H11)4N+ cation occupies a four-chamber cavity built of 15-hedra 71635942 (idealized description), with small vacant 5444 cavities filling the intervening space.
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 17 (1994), S. 187-201 
    ISSN: 1573-1111
    Keywords: β-Cyclodextrin ; sulfathiazole ; inclusion complex ; crystal structure ; thermal analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An inclusion complex with the formula (β-cyclodextrin) (sulfathiazole) 8.3 H2O has been crystallized and characterized by physicochemical methods including single crystal X-ray analysis. The complex crystallizes in the monoclinic system, space group P21, witha=15.264(4),b= 16.500(6),c=15.559(5) Å,β=117.29(3)o andZ=2. The structure was solved using published co-ordinates forβ-cyclodextrin in an isomorphous complex. Refinement by block-diagonal leastsquares yieldedR=0.061 for 4706 unique observed reflections. Inclusion of sulfathiazole produces a slight ellipticity in the host conformation, but the guest adopts a conformation similar to that observed in its polymorphs. The guest is held in the macrocyclic cavity predominantly by hydrophobic forces, with the phenyl ring near the host primary hydroxyl side and the thiazole ring near the secondary hydroxyl side. The complex packs in layers parallel to theac-plane. Layers are linked by hydrogen bonding to water molecules which are located outside the cyclodextrin cavity. An extensive network of hydrogen bonds mediated chiefly by water molecules stabilizes the crystal structure.
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  • 19
    ISSN: 1573-1111
    Keywords: Gossypol ; complex ; crystal structure ; single crystal ; desolvation ; polymorph
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The structures of gossypol complexes are extremely sensitive to the halogenomethane present as the guest; e.g. changing the number of Cl atoms in chloromethane derivatives changes the structure of the gossypol complex. The crystals of C30H30O8·CH2Cl2 are monoclinic, space groupC2/c,a=21.320(4),b=19.199(6),c=15.765(2)Å, β=113.05(2)o,V=5916(2)Å3,Z=8,D x=1.35 g/cm3,T=295 K. The structure has been solved by direct methods and refined to the finalR value of 0.084 for 1828 reflections. In the structure H-bonded gossypol molecules form columns, generating channels in the structure which are filled by guest molecules. After decomposition (desolvation) monocrystals of the complexes are conserved without destruction, in which there are rather wide and empty channels though slightly smaller than in the complex. An attempt is made to explain some peculiarities of the behavior of the gossypol polymorph formed on the basis of its structure with empty channels.
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 17 (1994), S. 365-376 
    ISSN: 1573-1111
    Keywords: Gossypol ; inclusion compounds ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The crystal structure of a compound obtained in a condensation reaction of (±)-gossypol with (R)-(+)-phenylethylamine has been determined by X-ray structure analysis. The crystals of C46H48O6N2·(C4H8O2)2 are monoclinic, space groupP21,a=21.243(3),b=8.666(1),c=28.651(4) Å, β=108.24(1)0,V=5009(3) β3,Z=4,D x=1.195 g cm−3, μ(CuK α)=0.66 mm−1,T=292 K. The structure has been solved by direct methods and refined to the finalR value of 0.091 for 4290 observed reflections and 1049 parameters. There are two diastereoisomeric molecules of the host and four solvent molecules in the asymmetric unit. The host molecules are H-bonded into chains with diastereoisomeric molecules alternating along the chain. The fact that the host prefers the association mode in which molecules with a different configuration of the 2,2′-binaphthyl moiety are H-bonded explains why separation of diastereoisomeric diaminogossypols by fractional crystallization has been unsuccessful. The 1,4-dioxane molecules are accommodated in infinite channels but only every second guest molecule in a channel is H-bonded to the host.
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  • 21
    ISSN: 1573-1111
    Keywords: D,L-hexapeptide ; cyclic ; crystal structure ; stacks ; tubular ; β-rings ; channels
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An X-ray analysis of single crystals (from MeOH) of cyclo(-D-Leu-L-MeLeu-D-Leu-L-MeLeu-D-Leu-L-MeLeu-) has been carried out. The analysis reveals that the molecules of the cyclopeptide occur in the crystals with two slightly different, almost hexagonal backbone conformations of the β-type, and that pairs of molecules with the same conformation interact through their nonmethylated face, forming dimeric units (units A and B) with six interannular H-bonds. This kind of pairing reproduces well that expected for a two-ring element in a stack of antiparalleβ-rings. The X-ray analysis has also revealed the presence in the A units of two water molecules, each at one of two equivalent sites located on the 3-fold axis of the units and equidistant from the center of gravity, and the presence in the B units of one water molecule at the center of the units. This provides experimental support for the idea that stacks ofβ-rings can serve as molecular channels.
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  • 22
    ISSN: 1573-1111
    Keywords: Pentaborate ; boric acid ; clathrate ; diamond-related network ; hydrogen bonding ; tetrapropy-lammonium ; tetrabutylammonium ; crystal structure ; 11B MAS NMR ; 13C MAS NMR ; thermogravimetry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Single-crystal X-ray structure analyses of N(nPr)4[B5O6(OH)4][B(OH)3]2,1, and N(nBu)4 [B5O6(OH)4][B(OH)3]2,2, reveal that these materials are novel clathrates, the isotypic host structures of which are three-dimensional assemblies of hydrogen-bonded [B5O6(OH)4]− ionsand B(OH)3 molecules. The assembly of only the pentaborate anions is a distorted (i.e., along [102] elongated) fourconnected diamond-related network. The N(nPr) 4 + and N(nBu) 4 + ions are trapped within the complex three-dimensional channel systems of the host frameworks. Both1 and2 crystallize monoclinically with space groupP21/c andZ=4. The cell constants are:1:a=13.592(5),b=12.082(2),c=17.355(6) Å, β=106.60(2)° (298K);2:a=13.874(3),b=12.585(1),c=17.588(4) Å, β=107.04(1)° (238 K). The results obtained by both11B and13C MAS NMR spectroscopy are discussed. Thermogravimetric studies under a flowing inert-gas atmosphere suggest that water, stemming from polycondensation of the hydrous borate species, is released from the clathrates at ca. 443 K (1) and 398 K (2) before the decomposition of the organic cations starts at ca. 603 K (1) and 603 K (2).
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  • 23
    ISSN: 1573-1111
    Keywords: Calixarenes ; arenetricarbonylchromium ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The structures of three arene-tricarbonylchromium complexes prepared from cone and 1,3-alternate-25, 26,27,28-tetrapropoxycalix[4]arene(1) and Cr(CO)6 were determined by single crystal X-ray studies. Crystal data for 1,3-alternate-1·Cr(CO)3 are space groupP21/a,a=19.496(3)Å,b=11.118(2)Å,c=19.121(2)Å, β=109.95°(1) andV=3895Å3. The structure was refined toRw=0.068. Crystal data for cone-1·Cr(CO)3 are space groupP21/a,a=21.457(4)Å,b=12.184(1)Å,c=14.816(2)Å, β=91.61°(1) andV=3872Å3. The structure was refined toRw=0.077. Crystal data for cone-1·2Cr(CO)3 are space groupP21/a,a=18.019(3)Å,b=41.347(4)Å,c=11.743(2)Å, β=97.39°(1) andV=8676Å3. The single crystal included two similar but slightly different structures but the data were successfully refined toRw=0.092. The structure of 1,3-alternate-1·Cr(CO)3 differs only slightly from that of the regular 1,3-alternate calix[4]arene. In contrast, cone-1·Cr(CO)3 and cone-1·2Cr(CO)3 show an unusual conformation with a pair of faced gablelike roofs, which is considerbly distorted from the regular cone calix[4]arene. The origin of this distortion is discussed in combination with the spectral studies.
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  • 24
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 19 (1994), S. 4-13 
    ISSN: 0887-3585
    Keywords: trichosanthin ; ribosome-inactivating proteins ; crystal structure ; orthorhombic ; molecular replacement ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Trichosanthin (TCS) is one of the single chain ribosome-inactivating proteins (RIPs). The crystals of the orthorhombic form of trichosanthin have been obtained from a citrate buffer (pH 5.4) with KC1 as the precipitant. The crystal belongs to the space group P212121 with a = 38.31, b = 76.22, c = 79.21 Å. The structure was solved by molecular replacement method and refined using the programs XPLOR and PROLSQ to an R-factor of 0.191 for the reflections within the 6-1.88 Å resolution range. The bond length and bond angle in the protein molecule have root-mean-square deviations from ideal value of 0.013 Å and 3.3°, respectively. The refined model includes 247 residues and 197 water molecules. The TCS molecule consists of two structural domains. The large domain contains six α-helices, a six stranded sheet, and an antiparallel β-sheet. The small domain has a largest α-helix, which shows a distinct bend. The possible active site of the molecule located on the cleft between two domains was proposed. In the active site Arg-163 and Glu-160, Glu-189 and Arg-122 form two ion pairs, Glu-189 and Gln-156 are hydrogen bonded to each other. Three water molecules are bonded to the residues in the active site region. The structures of TCS molecule and ricin A-chain (RTA) superimpose quite well, showing that the structures of the two protein molecules are homologous. Comparison of the structures of the TCS molecule in this orthorhombic crystal with that in the monoclinic crystal indicates that there are no essential differences of the structures between the two protein crystals. © 1994 Wiley-Liss, Inc.
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  • 25
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 20 (1994), S. 149-166 
    ISSN: 0887-3585
    Keywords: crystal structure ; cold adaption ; catalytic efficiency ; protein stability ; anionic ; ectotherm ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The crystal structure of an anionic form of salmon trypsin has been determined at 1.82 Å resolution. We report the first structure of a trypsin from a phoikilothermic organism in a detailed comparison to mammalian trypsins in order to look for structural rationalizations for the cold-adaption features of salmon trypsin. This form of salmon trypsin (T II) comprises 222 residues, and is homologous to bovine trypsin (BT) in about 65% of the primary structure. The tertiary structures are similar, with an overall displacement in main chain atomic positions between salmon trypsin and various crystal structures of bovine trypsin of about 0.8 Å. Intramolecular hydrogen bonds and hydrophobic interactions are compared and discussed in order to estimate possible differences in molecular flexibility which might explain the higher catalytic efficiency and lower thermostability of salmon trypsin compared to bovine trypsin. No overall differences in intramolecular interactions are detected between the two structures, but there are differences in certain regions of the structures which may explain some of the observed differences in physical properties. The distribution of charged residues is different in the two trypsins, and the impact this might have on substrate affinity has been discussed. © 1994 Wiley-Liss, Inc.
    Additional Material: 10 Ill.
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  • 26
    ISSN: 1573-9171
    Keywords: organic conductors ; ion-radical salts ; bis(ethylenedithio)tetrathiafulvalene ; mercury iodides ; crystal structure ; electrochemical synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new cation-radical salt (ET)4[Hg2I6] (1), where ET is bis(ethylenedithio)tetrathiafulvalene, has been synthesized in the system ET-HgI3 −-PhCl. An X-ray study of 1 (a=41.02(5),b=23.01(1),c=8.233(2) Å,V=7772(3) Å3, space groupPc21 b,Z=4,d calc=2.308 g cm−3) has established its composition, chemical formula, and the main structural features. The ET cation-radicals are packed in the conducting layer, the type of packing is α″; the [Hg2I6]2− anion has a dimeric structure. The temperature dependence of the conductivity of the (ET)4[Hg2I6] crystals (σ300=6 Ohm−1 cm−1) has a semiconducting character.
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  • 27
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 43 (1994), S. 1384-1389 
    ISSN: 1573-9171
    Keywords: synthesis ; macrocyclic thiophenylene ketone ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The side reaction of macrocyclization that occurs during the synthesis of poly-(1,4-phenylenesulfide ketone) by polycondensation of a 4,4-dihalobenzophenone with sodium sulfide was studied. It was found that the major product of this reaction is a cyclic trimer, cyclotris-(4,4"-thiodiphenylene ketone) (1). Despite the fact that ketone bridges are more rigid than sulfide bridges, the yield of the macrocycle is rather high, as it is in the synthesis of poly-(1,4-phenylenesulfide), and reaches 20% under high dilution conditions. The structure of 1 was investigated by X-ray diffraction analysis (R = 0.069 on 3138 reflections). Macrocycle 1 is strongly flattened in the crystal; the conformation observed is determined by the packing, since stereochemical analysis indicates high flexibility of the macrocycle. The solvate acetone molecules incorporated in the crystal are disordered, nevertheless, they are strongly fixed in the cavities and channels of the crystal structure.
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  • 28
    Electronic Resource
    Electronic Resource
    Springer
    Journal of sol gel science and technology 1 (1994), S. 113-121 
    ISSN: 1573-4846
    Keywords: crystal structure ; complexing agent ; TiO2 ; TiO2-SiO2
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Many types of TiO2-SiO2 (Ti:Si=50:50 mol%) were prepared by the sol-gel procedure with and without 2-methyl-2, 4-pentanediol (MPD) as an organic ligand. The effect of MPD on the gel structure and the properties of the TiO2 crystals were studied by XRD and raman spectroscopy, and the effect of the sol standing time on the properties of the TiO2 crystals were also studied by XRD spectroscopy. In the gels with MPD, anatase of TiO2 appeared at approximately 580°C, and the crystal structures were similar despite the difference in the gel preparation procedure. The titania gels with MPD were presumed to be dispersed in the silica gel matrix without any Ti-O-Si bond. In the presence of MPD, the formation of titania gels is controlled and the specified TiO2 crystal is produced.
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  • 29
    ISSN: 1573-9171
    Keywords: C60·2S8 ; fullerene complexes ; synthesis ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The C60·2S8 complex was prepared by reaction of buckminsterfullerene C60 with sulfur in trichloroethylene and its single-crystal X-ray structure was studied at room temperature. Crystals of this compound are monoclinic, space groupC 2/c, a=20.90(1),b=21.10(1),c=10.537(9) Å, β=111.29(7)°,Z=4,d calc=1.89 g·cm−3. The crystal structure of the C60·2S8 complex consists of packed fullerene molecules that form hexagonal channels along thec axis with eight-membered crown-shaped S8 cyclic molecules inside the channels. The distances between the centers of neighboring fullerene molecules are 10.036(7), 10.636(7), and 10.537(9) Å. Each C60 molecule is linked to eight S8 molecules with ten shortened intermolecular contacts C...S 3.41(1)–3.52(2) Å. The average values of the C=C and C-C bond lengths are 1.32(3) and 1.47(3) Å, which attest to a significant degree of localization of electron density in the c60 molecule.
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  • 30
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2289-2306 
    ISSN: 0887-6266
    Keywords: poly(ethylene terephthalate) ; fiber ; x-ray diffraction ; crystal structure ; three-phase model ; modulus ; tenecity ; shrinkage ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The structure of four semicrystalline poly(ethylene terephthalate) fibers were analyzed with full-pattern (two-dimensional Rietveld) x-ray diffraction refinement, small-angle x-ray scattering, and thermal mechanical analysis, and compared to some of their known mechanical properties. The classical two-phase model of crystal and amorphous phases were unable to correlate structure and properties. We found that there must be a third phase, an oriented, intermediate phase, located mainly between the fibrils. About 1/3 of the intensity of fiber diffraction of the analyzed samples was contributed from such intermediate phase. For some fiber properties the intermediate phase plays a similar role as proposed for “taut tie molecules.” A simple model for the description of structure-insensitive properties of PET fibers was developed, based on this quantitaitve separation into three phases. The oriented intermediate phase changes the definition and calculation of the basic parameters of the fiber structure, such as crystallinity and orientation. Based on small-angle x-ray evidence, the crystallites are assumed to be separated by layers of largely amorphous material, both surrounded by the intermediate phase. The initial modulus of the fiber is determined mainly by the amount and orientation of the intermediate phase which has a maximum modulus of about 500 g/d on full orientation instead of the earlier predicted 150 g/d for fully oriented semicrystalline fibers. Based on the relationship between tenactity and average orientation function, the maximum tenacity for PET fibers of a structure like the ones analyzed may reach 20-45 g/d instead of earlier predictions of 10 g/d. The additional information needed to understand the structure-sensitive property of shrinkage is discussed. Presently easily accessible parameters have no quantitative predictive capabilities. © 1994 John Wiley & Sons, Inc.
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  • 31
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 851-857 
    ISSN: 0887-6266
    Keywords: rigid rod polymer ; thermotropic ; aromatic polyester ; oriented film ; thermal expansion ; crystal structure ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The linear thermal expansion coefficients of oriented films of poly(p-phenylene-2,5-didodecyloxy-terephthalate) in the three structures B, A, and Lf are reported. The results are interpreted in terms of a molecular laminate model in which the rigid main-chain layers are separated by the aliphatic side chains. In a film oriented unidirectionally the rigid mainchain layers provide a negative contribution to the thermal expansion coefficient, while the side chains supply a positive contribution. Therefore, the resulting expansion coefficient α depends on the details of the main- and side-chain packing and low-temperature values between α = +0.3 × 10-5 K-1 (A and Lf and α = -1.2 × 10-5 K-1 (B) are found in highly oriented films. Measurements on undrawn films are in accordance with the molecular laminate model. © 1994 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
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  • 32
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    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 2653-2659 
    ISSN: 0887-6266
    Keywords: tetraalkylammonium halide ; atomic force microscopy ; crystal structure ; surface structure ; hextriacontane ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The surface structures of two series of tetra-n-alkylammonium halides, N(CxH2×+1)4I and N(CxH2x+1)4 Br have been investigated with atomic force microscopy (AFM) and compared to hexatriacontane (C36H74). The surfaces could be imaged with atomic resolution. The observed primitive, square surface-patterns of tetra-n-butyl chloride and bromide are in good accord with x-ray single-crystal structure. For n 〉 4, x-ray powder diffraction showed that increasing the alkyl chain-length leads mainly to an appropriate increase of the unit cell along the c-axis, which suggests similar layer structures for all long-chain salts beyond the butyl homologue. Within the centers of the molecular layers of these crystals reside the halide anions and the quaternary nitrogens. The surfaces accessible for AFM consist of methyl end-groups. As the number of carbon atoms increases beyond four, the surface symmetry changes to the face-centered square patterns characteristic of many paraffins. The chains of the tetraalkyl ammonium salts pack, however, less dense than paraffins. © 1994 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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  • 33
    ISSN: 0009-2940
    Keywords: Germane, optically active ; Biotransformation, stereoselective ; Transesterification, enzymatic ; Porcine liver esterase ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of ( - )-(Acetoxymethyl)(hydroxymethyl)methyl(phenyl)germane [( - )-MePhGe(CH2OAc)(CH2OH)] by an Esterase-Catalyzed Transesterification: the First Enzymatic Synthesis of an Optically Active GermaneThe prochiral germane MePhGe(CH2OH)2 (1) was synthesized by a six-step synthesis starting from GeCl4 (3) [3 → Cl2Ge(CH2Cl)2 (4) → Ph2Ge(CH2Cl)2 (5) → (CF3S(O)2O)PhGe(CH2Cl)2 (6) → MePhGe(CH2Cl)2 (7) → MePhGe(CH2OAc)2 (8) → 1]. Reaction of 1 with Ac2O/NEt3 (molar ratio 1: Ac2O = 1:1) gave the racemic germane rac-MePhGe(CH2OAc)(CH2OH) (rac-2). Stereoselective transesterification of 1 with vinyl acetate (acetate source and solvent), catalyzed by immobilized porcine liver esterase (PLE; E.C.-3.1.1.1), yielded the optically active germane ( - )-MePhGe(CH2OAc)(CH2OH) [( - )-2] (yield 57%, enantiomeric purity 50% ee).
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  • 34
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 91-92 
    ISSN: 0009-2940
    Keywords: Boranes, amino(imino) ; Iron, tricarbonyl(butanone) ; Diiron, [(boryloxy)allyl]hexacarbonyl ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Formation of a Fe2(CO)6 Complex with a (Boryloxy)allyl BridgeThe amino(imino)borane Me3Si(tBu)N=B=NtBu (1) reacts with (benzylideneacetone)tricarbonyliron (2) in 1:2 molar ratio to give a 50% yield of the hexacarbonyldiiron complex 3 with a fly-over (boryloxy)allyl bridge, which crystallizes in the space group P21/c. The structure of 3 can be described as a pyramid with Fe(CO)3 at the apex and a non-planar pentagon [-Fe(CO)3-O(BXX′)-C(Me)-CH-C(Ph)-] [X = NHtBu, X′ = N(SiMe3)tBu] as the basis, but there is no bond between the apex and the O atom.
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  • 35
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 107-112 
    ISSN: 0009-2940
    Keywords: Bis(pentamethylcyclopentadienyl)methanol ; Diels-Alder reaction, intramolecular ; Chloroformate, bis(pentamethylcyclopentadienyl)methanol ; Tosylate, bis(pentamethylcyclopentadienyl)methanol ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(pentamethylcyclopentadienyl)methanol: Synthesis, Structure, and DerivatizationBis(pentamethylcyclopentadienyl) ketone (1) reacts at low temperatures with LiAlH4 to form in good yields (pentamethylcyclopentadienyl)methanol (2) and its corresponding intramolecular Diels-Alder product 3 in a ca. 2:1 ratio. The alcohol 2 is separated from the tetracyclic compound 3 by crystallisation at -70°C from hexane/pyridine as pyridine adduct. The pyridine-free alcohol 2 is available by repeated dissolving of the adduct in hexane and removal of the volatile components in vacuo. The alcohol tends to intramolecular [4 + 2] cycloaddition even at room temperature with formation of 3. A derivatization of 2 is possible by deprotonation with alkyllithium compounds, which leads to the alcoholate 4, and subsequent treatment with phosgen and tosyl chloride, thus affording the chloroformate 6 and the tosylate 7, respectively, in good yields. The thermolabile tosylate 7 decomposes to pentamethylbenzene or, under basic conditions, to the pentacyclic compound 7.
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  • 36
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 145-149 
    ISSN: 0009-2940
    Keywords: Bis(trifluormethyl)butenal ; Retinoids ; β-Ionol ; Fluoro compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preparation of Suitable Precursors for the Synthesis of 16,16,16,17,17,17-HexafluororetinalsCycloaddition reactions of (CF3)2C = CHCHO with butadiene or 1,3-pentadiene provide the corresponding cyclohexane derivatives 2, 3 and 4. Condensation of 3 with (C2H5O)2P-(O)CH2C(O)CH3 or of 2 with acetone in the presence of bases yields 5 and 7. While 5 reacts with CH2 = CHMgBr to give 6, treatment of 7 with diluted HCI provides 8. Compounds 7 and 8 proved to be not suitable as starting materials for the preparation of 16,16,16,17,17,17-hexafluororetinals. A better synthon is the diene 11. This is obtained in a threestep reaction starting from hexafluoroacetone and (C6H5)3P=CHC(O)CH3 to give 9 which on treatment with CH3MgI provides 10. Dehydration of 10 with 50% H2SO4 forms 11. In this reaction sequence byproduct 12 is formed presumably by addition of CF3C(O)CF3 to 9. At elevated temperatures under pressure 11 adds ethylene to form 13. Functionalization of 13 in 2-position is achieved by hydroboration/oxidation yielding 14 which is oxidized with pyridinium dichromate to 15. Oxidation and bromination reaction of 13 are described.
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  • 37
    ISSN: 0009-2940
    Keywords: Carbonyl olefination ; Molbydenum aluminium complexes, organo ; Tungsten aluminium complexes, organo ; Tebbe reagent ; Aluminium, molybdenum and tungsten complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organomolybdenum and Organotungsten Reagents, VI[1]. On the Carbonyl-Methylenating Molybdenum-Aluminium and Tungsten-Aluminium μ-Methylene ComplexesMoCl5, MoOCl3(THF)2, MoO2Cl2, (MeO)2MoCl3, (MeO)4MoCl, WOCl3(THF)2, and WOCl4 form carbonyl-methylenating complexes and 1-2 equiv. of CH4 by reacting with 2 equiv. of Me3Al. These thermolabile complexes are prepared in solution and differ in their properties (e.g. ability to transfer mostly more than 1 CH2 unit per Mo or W atom in carbonyl-olefinating processes; high sensitivity to water, no hydroxy ketone affinity) from the carbonyl-olefinating 1,3-dimetallacyclobutanes (M = Mo, W) and are believed to be mono- and bicyclic analogs (e.g. hypothic structures 3, 6-8) of the Tebbe reagent (1), containing Mo-μCH2 Al or W -μCH2 Al groups, respectively. Analogous complexes seem to be produced by treating MoOCl3(THF)2 with 2 Me2Zn or (MeO)2MoCl3 and (MeO)4MoCl with 2 MeMgBr in each case. Unlike the dimeric and, due to a Mo—Mo bond, diamagnetic Mo derivatives (Me—O)2MoCl3 and (MeO)4MoCl (according to 1H—NMR structure 9 or 10 and 11 or 12, respectively) the complexes obtained by the reactions (MeO)2MoCl3 + 2 Me3Al and (MeO)4MoCl + 2 Me3Al are paramagnetic, indicating the expected absence of a Mo—Mo bond. The 1H—NMR spectrum of the reaction mixture obtained by treating the MoVI derivative MoO2Cl2 with 2 Me3Al in THF shows various signals for μ—CH2 groups, whereas signals of t-CH2 ligands are missing (t = terminal). In analogy to 1 the carbonyl-olefinating activity of the Mo—Al and W—Al reagents is activated by the addition of 2 equiv. of HMPA. Treatment of PhCOCH2NEt2 (19) with {MoO2Cl2 + 2 Me3Al} leads to carbonyl olefination with formation of 20 and also to α-methylation with formation of PhCOCH(Me)-NEt2 (21), pointing to the intermediate formation of a t-CH2—Mo ligand. {MoO2Cl2 + 2 Me3Al + 2 HMPA} has found to be the best reagent for the carbonyl olefination of aldehydes, whereas {WOCl3(THF)2 + 2 Me3Al + 2 HMPA} was optimal for ketones. In 1:1 reactions both reagents normally give better yields than the Tebbe reagent. By applying (WOCl3(THF)2 + 2 Me3Al} and {MoO2Cl2 + 2 Me3Al} on ketones 16-18 an interesting neighbour group effect of electron donor atoms in the δ position to the keto group was observed.
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  • 38
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 191-200 
    ISSN: 0009-2940
    Keywords: Diazo compounds ; Valence isomerization ; „Corset effect“ ; limits of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Small Rings, 79[1].  -  Synthesis and Properties of Novel Silyl-Substituted Cyclobutadienes and TetrahedranesThe cyclobutadienes 2b, d as well as the corresponding tetrahedranes 3b, d have been prepared according to the “Masamune route” by starting from the diazo compounds 1b, d. Low-temperature 13C—NMR measurements of the cyclobutadienes 2a, b, d lead to the first exact values of the barrier heights in the interconversion of the two rectangular forms of the cyclobutadienes. Fluorodesilylation of 3d probably proceeds via tri-tert-butyltetrahedrane (3h) and cyclobutadiene 2h and finally yields diketone 18. Reaction of tetrahedrane 3d with LiAlH4 in boiling THF leads to tetrahedrane 3e, which is much less stable than all previously known tetrahedrane derivatives.
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  • 39
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 213-217 
    ISSN: 0009-2940
    Keywords: Alkylation ; Alkoxyalkylation ; Carboxonium ions ; Acetals ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Competition experiments have been performed to determine the relative reactivities of acetals and ethers toward allyltrimethylsilane in the presence of catalytic amounts of BF3 OEt2. It is found that acetals R-CH(OMe)2 and their phenylogous p-anisyl ethers R-CH(p-MeOC6H4)(OMe) show very little differences in reactivity. The reactivity scales are employed to rationalize the results of Lewis acid-catalyzed additions of acetals and ethers to CC double bonds.
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  • 40
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 237-245 
    ISSN: 0009-2940
    Keywords: Cyclopropenes, 3,3-dimethyl-1-trimethylsilyl-substituted ; Cyclopropene, isomerisation ; Gas-phase kinetics ; Ring opening ; Diradical intermediates ; Cyclopropylidene intermediates ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The gas-phase pyrolyses of 1,3,3-trimethyl-2-(trimethylsilyl)-cyclopropene (9), 3,3-dimethyl-1,2-bis(trimethylsilyl)cyclopropeneTextReactantlog (A/s-1)Ea/kj mol-1(kcal mol-1)913.41 ± 0.22192.1 ± 2.5(45.9 ± 0.6)1013.54 ± 0.19184.4 ± 2.1(44.1 ± 0.5)1112.17 ± 0.38124.6 ± 3.1(29.8 ± 0.7)(10), and 3,3-dimethyl-1-(methylthio)-2-(trimethylsilyl)cyclopropene (11) have been studied, and the pressure-independent Arrhenius parameters listed in the table were obtained. All three rearrangements are homogeneous, first-order and unimolecular reactions. Rather surprisingly all reactions give the corresponding isomeric allenes as the main products. Amongst possible mechanisms discussed, 10 is proposed to react via a cyclopropylidene intermediate, whilst the results for 9 and 11 throw light on the relative importance of the diradical- and vinylcarbene-type intermediates produced by cyclopropene ring opening.
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  • 41
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A5 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 42
    ISSN: 0009-2940
    Keywords: Metal dithiolenes ; Dipyridinioethylene dihalides ; Charge-Transfer complexes ; Electrical conductivity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Charge-Transfer Complexes of Metal Dithiolenes, XIII[1]. - cis-trans-Photoisomerisable Viologens as Redoxactive Acceptors  -  Synthesis and Electrical ConductivityIon Pair Charge-Transfer (IPCT) complexes of the type [A2+[ML2]2-} (1a-f to 4a-f) are synthesized from dianionic metal dithiolenes [M = Ni, Zn, L = cis-1,2-dicyano-1,2-ethene-dithiolate (mnt2-), 2-thioxo-1,3-dithiol-4,5-dithiolate (dmit2-)] and dicationic viologens [A2+ = 4,4′-(1,2-ethenediyl)bis(1-alkylpyridinium)]. The acceptors can exist as cis/trans isomers and may have coordinating properties in the case of 1-cyanoalkyl groups. The IPCT bands are in the range of 500 to 1200 nm and their energy follows the Hush-Marcus relation. For the nickel complexes the reorganization energy amounts to 73, for the zinc compounds to 115 kJ/mol. As shown by X-ray analysis of {A2+[Ni(mnt)2]2-} (2d), A2+ = trans-4,4′-(1,2-ethenediyl)-bis[1-(3-cyanopropyl)pyridinium], the structure consists of stacks of alternating donors and acceptors with a typical plane-to-plane distance of 350 pm. There is no interaction between the cyano group of the acceptor and the nickel atom of the donor. The electrical conductivities of the nickel compounds are in the range of 5 · 10-6 to 3 · 10-11 Ω-1 cm-1, and the corresponding activation energies vary from 0.24 to 0.61 eV. For the dmit complexes these values agree well with the free activation enthalpy of the electron transfer reaction A2+ + [ML2]2- → A+ + [ML2]- calculated from the Hush-Marcus model. This suggests that charge carrier generation occurs by electron transfer. When a trans acceptor is replaced by its cis isomer in [A2+[NiL2]2-}, conductivity changes from 5 · 10-7 to 5 · 10-6 Ω-1 cm-1 and the activation energy from 0.43 to 0.24 eV, when L - dmit2- but stays at about 1 · 10-8 Ω-1 cm-1 for L = mnt2-.
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  • 43
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 44
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 11-14 
    ISSN: 0009-2940
    Keywords: Niobium iodide telluride ; Polytellurides ; Chain compounds, one-dimensional ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new ternary compound Nb4Te17I4 has been prepared and structurally characterized. It crystallizes in the monoclinic system, space group C2/c with unit-cell parameters a = 16.199(4), b = 8.128(2), c = 27.355(6) Å, β = 110.84(2)°, Z = 4. The structure consists of infinite one-dimensional niobium/tellurium chains running parallel to the crystallographic c direction. The chains are separated by iodine atoms. Short and long metal-metal distances alternate in the sequence of three consecutive short bonds ([d ≈ 3.1 - 3.2 Å) and one long (d = 4.268 Å) metal-metal separation. Each Nb atom is eight-coordinate. The composition of the chain is ∞11[(Nb5+)2(Nb4+)2(Te22-)4(Te32-)3(I-)4].
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  • 45
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 15-21 
    ISSN: 0009-2940
    Keywords: Copper niobium telluride ; Layer compounds ; Low-dimensional compounds ; Electrical properties ; Band structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis, Structure and Electronic Properties of Cu0.69NbTe2Cu0.69NbTe2 is obtained from the elements in a sealed quartz ampoule at 850°C. The structure of Cu0.69NbTe2 is related to the CdI2 type. The Cu atoms are disordered and situated in tetrahedral sites between the NbTe2 layers. The Nb atoms form zig-zag chains extending in one direction within the layers. This deformation of the Nb sublattice from trigonal symmetry is typical for CdI2 derivatives with formal electron counts close to d2 on the early transition metal. The magnetic susceptibility is temperature-independent between 4 K and 300 K (Pauli paramagnetism). Resistivity measurements confirm the metallic behavior of the compound. The crystal structure and the physical properties are in agreement with the results of tight-binding band-structure calculations.
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  • 46
    ISSN: 0009-2940
    Keywords: (Trifluoromethyl)sulfane- and -disulfanesulfonic acids ; Mercury compounds ; (Trifluoromethyl)sulfanyl-disulfanyl-, and -sulfinylimine ; Arsenic compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Properties of S-(Trifluoromethyl)polysulfanemonosulfonates CF3SxSO2M [x=1, M = OH, NH4O, 1/2 HgO2, (CH3)2N, NH2; x=2, M = NH4O]*Hydrolysis of CF3SNSO with 2 equiv. of H2O provides [NH4][CF3SSO3] (1), which on treatment with chlorine gives CF3SCl and [NH4][ClSO3]. Trifluoromethyl thiosulfates are synthesized from Hg(SCF3)2 and ClSO2M [M = NH4O, (CH3)3SiO (2), (CH3)2N (3), NH2 (4)]. Insertion of SO3 into Hg(SCF3)2 provides Hg[CF3SSO2O]2 (6). Similarly, S-(trifluoromethyl)thiosulfuric acid (5) is obtained from CF3SH and SO3. New preparations for CF3SXNSO (x=1, 2) are described. These compounds are formed either from Hg(NSO)2 or (CH3)3SiNSO and CF3SxCl in good yields. CF3SSNSO (8) reacts with water to give [NH4][CF3SSSO3] (9). A 1:1 adduct (10) is obtained from CF3SNSO and AsF5. A preliminary X-ray structure investigation proved that AsF5 is coordinated to the oxygen atom. Some reactions of [NH4][CF3SSO3] and CF3SSO2OSi(CH3)3 are mentioned.
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  • 47
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 501-506 
    ISSN: 0009-2940
    Keywords: Tripod ligand synthesis ; Tripod iron trisacetonitrile complexes ; Tripod cobalt acetate complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Functionalized Tripod Ligands: Synthesis and Coordination of 1,1,1-Tris[(diphenylphosphanyl)methyl]methaneThe tripod ligand HC(CH2PPh2)3 (4) is easily available from the reaction of 1,3-dichloro-2-(chloromethyl)propane (3) with lithium diphenylphosphide. The ligand 4 itself and two of its coordination compounds, [(HC(CH2PPh2)3)Co(OOCMe)]+-[BPh4]- (5 · BPh4) and [(HC(CH2PPH2)3)Co(OOCMe)]2+ · 2[BF4]- [7 · (BF4)2] have been characterized by X-ray analyses. Coordination of 4 leads to an opening of the CH2—CH—CH2 bond angles (114° in 7 · (BF4)2 and 5 · BPh4 versus 111° in 4). This change in structure is reflected by the unusual low field shift of the methine hydrogen of 7 · (BF4)2 (δ = 3.90) in comparison with the corresponding signal of the free ligand 4 (δ = 1.53).
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  • 48
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 525-531 
    ISSN: 0009-2940
    Keywords: Alkynes ; Alkenes ; Nucleophilicity ; Carbenium ions ; Vinyl cations ; Kinetics ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relative reactivities of alkenes and alkynes toward diarylmethyl cations have been determined by direct rate measurements and by competition experiments in dichloromethane. At -70°C alkynes are found to be one to two orders of magnitude less reactive than analogously substituted alkenes (e.g. phenylacetylene/styrene), but the reactivity difference reduces strongly as the temperature is raised. The stereochemistry of the vinyl chlorides produced by addition of benzhydryl chlorides to alkynes is characterized.
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  • 49
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 205-212 
    ISSN: 0009-2940
    Keywords: Alkylation ; Allylation ; Carbenium ions ; Friedel-Crafts reactions ; Linear free energy relationships ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Competition experiments have been performed to determine the relative reactivities of 23 alkyl chlorides toward allyltrimethylsilane in the presence of catalytic amounts of ZnCl2.The krel scale spans over 11 orders of magnitude from 1-adamantyl chloride (least reactive) to bis(p-methoxyphenyl)methyl chloride (most reactive compound). A fair correlation between the alkylating ability and the SN1 reactivity in solvolysis reactions is found, thus providing a quantitative basis for our long-standing working hypothesis that Lewis acid-catalyzed additions of alkyl halides to CC multiple bonds only yield 1:1 products if the reactants ionize faster than the products. Trityl chlorides do not follow this correlation and are 105 times less reactive than predicted from their SN1 reactivities.
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  • 50
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 231-236 
    ISSN: 0009-2940
    Keywords: Zinc porphyrin complexes ; Porphyrin-quinone cyclophanes ; Photoinduced electron transfer ; Electron-transfer mechanism in metalloporphyrin-quinone cyclophanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to increase the driving force for photoinduced electron-transfer reactions of porphyrin-quinone cyclophanes, the zinc complexes 3a-e and 4a-e were prepared from the corresponding cyclophanes of the 1 and 2 series. Electron-transfer-related properties like redox potentials and fluorescence spectra were determined for 3a-e and 4a-e. The X-ray structure analysis of 4a indicates that for the very fast and solvent-independent electron transfer in these systems a specific mechanism involving an interaction of a quinone carbonyl group with the zinc might be considered as an alternative to through-space electron-transfer.
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  • 51
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 247-259 
    ISSN: 0009-2940
    Keywords: Pyrroles, heteroannulated ; α-Pyridones, heteroannulated ; Pentalenes, dihetero- ; Nitrones ; Heterocyclizations, 1,7-dipolar ; Diels-Alder reactions ; Singlet oxygen ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A Novel Route to Isoannulated Heteroaroamtic Compounds, 2[1].  -  The Dipole Route to Furo/Thieno Pyrroles and α-Pyridones, and Their Benzo DerivativesA new methodology involving 1,7-dipolar cyclizations of conjugated dipoles followed by a multistep rearrangement affording ring-contracted products has been employed for the synthesis of various examples of the title compounds. Under different thermolysis conditions the annulated alkynyl nitrones 15-19, 45, and 46 are converted into isoannulated pyrroles and α-pyridones, respectively, with yields up to 90% (general reaction A → B + C). The product distribution is strongly influenced by the nature of the terminal substituent R, hence supporting a mechanism with oxo carbenes as central intermediates which undergo either 6-π cyclization to the pyrrole systems or Wolff rearrangement leading to conjugated ketenes, the precursors of the observed α-pyridones (see Scheme 1). Diels-Alder reactions were performed with benzofuropyridone 40a, napthopyridone 62 as well as with the corresponding dihydronaphtho compounds 64a, b. Whereas the tert-butyl derivatives 22b, 23b and 41b are rather unreactive against dienophiles, they are easily transformed into the cyclic imides 31, 32 and 52, respectively, under the influence of oxygen and light suggesting the formation and subsequent [4 + 2] cycloaddition of 1O2 as important steps.
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  • 52
    ISSN: 0009-2940
    Keywords: Metallocenes, dinuclear, silyl-bridged ; Antiferromagnetism ; Cyclic voltammetry ; Paramagnetic NMR spectroscopy ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dilithium salt of the 3a,4,7a,8-tetrahydro-4,4,8,8-tetra-methyl-4,8-disila-s-indacenediyl dianion (L2-, 2) was allowed to react with the solvated metal halides MX2 (M = Ni, Co, Cr) in the presence of the cyclopentadienyl (Cp) anion to give trans-CpMLMCp (3NiNi, 3CoCo, and 3CrCr) in yields up to 80%. The only cis isomers which could be detected were 4NiNi and 4CoCo. Similarly, the reaction of 2 with [CpVCl(PEt3)]2 gave the trans-vanadium analogue 3VV while the successive reaction of 2 with CrCl3 (THF)3 and PEt3 yielded the bridged half-sandwich (Et3P)Cl2CrLCrCl2(PEt3) (5CrCr). The mixed-metal dinuclear metallocene CpFel—NiCp (3FeNi) was synthesized from CpFel-, Cp- and solvated NiBr2. The molecules were characterized by mass spectrometry, elemental analyses, cyclic voltammetry, 1H—, 13C—, and 29Si—NMR spectroscopy and solid-state magnetic measurements. Cyclic voltammetry showed up to six electron transfers per molecule. A metal-dependent splitting of the half-wave potentials of up to 355 mV indicated rather strong electrostatic interaction between the metallocene units. The NMR results established unpaired spin on the ligands. Its distribution within the bridging ligand was correlated with the molecular orbital splitting and the magnetic interaction. Antiferromagnetic interaction was found for 3NiNi, 3CrCr, and 3VV with J = -11.6, -2.56, and -1.34 cm-1, respectively (H = -J · SA · SB). A temperature-dependent folding of the bridging ligand was deduced from the temperature behavior of the 1H—NMR signal shifts.
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  • 53
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 313-319 
    ISSN: 0009-2940
    Keywords: Phosphirene imines ; 1,2-Diphosphete diimines ; Isomerization ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Investigations of the System Phosphirene Imine/Iminophosphane - Insertion and Isomerization ReactionsTreatment of the iminophosphanes R1P=NR2 1 [R2 = tBu, R1 = Et3C (a); R2 = Aryl, R1 = Et (b), Me (c)] with 1,4-diphenyl-butadiyne (2) leads to the phosphirene imines R1-(R2N=)P̌(Ph)=CCCPh 3a-c and [R1(R2N=)P̌(Ph)=CC]2 4a-c. Further reaction with 1a, c gives the 1,2-diphosphetes R1(R2N=)PP(R1)(=NR2)C(Ph)=CCCPh 5a, b, which isomerize in the case of R1 = Me into the triphosphabicyclo[3.2.0]-hepta-1,6-diene 7. In the reaction of the phosphirene imines R1(ArylN=)P̌(R2)=C(R2) 3 [R1 = Me, R2 = Ph (d); R1 = Et, R2 = COOMe (e)] with the iminophosphanes 1b, d the initially formed diphosphetes 9a, b isomerize to the 1,2-diazaphosphole Cl(Mes*N=)PN(Mes*)P(Me)C(Ph)=C(Ph) 10 or the dioxadiphosphabicyclooctadiene C=C(OMe)OP(=N-Mes*)(Et)C=C(OMe)OP(=NMes*)(Et) 12 depending on the substituents. A reaction of the phosphirene imine 3d with dimethylamino-borane furnishes the vinylphosphane. Ph(H)C=C(Ph)P(Et)N(H)Mes* (14) by ring opening. The compounds 7, 10, 12 have been characterized by X-ray structure analyses.
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  • 54
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 359-365 
    ISSN: 0009-2940
    Keywords: Diastereoselectivity ; Effect, kinetic ; Effect, stereoelectronic ; Etherification ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stereoelectronic Effects and Chiral Recognition, I.  -  Diastereoselective Formation of Ethers from AlkylarylcarbinolsAcid-catalysed etherification of various alkylarylcarbinols 1 leads to a mixture of diastereomeric products 2 and 3. As found in the closely related formation of diastereomeric acetals, the ratio 2/3 is shown to be time-dependent. Preferred formation of the meso-diastereomer 3 under kinetic condition and preferred formation of the racemic diastereomer 2 under thermodynamic conditions is observed. A reaction path based on π-π interactions and stereoelectronic effects is presented to explain experimental results.
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  • 55
    ISSN: 0009-2940
    Keywords: 1,2-Dithiines ; Thioindigo ; Thioketones ; Disulfides, cyclic, molecular structure and reactions ; Valence isomerization, electrocyclic ; Thiophenes, derivatives of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(benzo[4,5]thieno)[3,2-c:2′,3′-e][1,2]dithiin, ein Valenzisomer von „Dithioxo-thioindigo“3-Mercaptobenzo[b]thiophene (1) is transformed with assistance of bases, especially of amines, into the benzo[b]-thieno-annellated 1,2-dithiine 6 and not into the originally claimed “Dithioxo-thioindigo” trans-3. Primarily, the formation of 6 from 1 involves oxidation to the disulfide 4 which may also be used separately. Conceivable rationalizations are discussed. The same compound is accessible (in lower yield)by thionation of thioindigo with the aid of the Lawesson reagent. X-ray elucidation of 6 reveals a non-planar structure of the cyclic disulfide with a dihedral C—S—S—C-angle of 53°. Despite of the absence of any established chromonphoric moiety, 6 is deeply red in the crystal and in solution, as it is representative for the “undisturbed” 1,2-dithiine system. Contrary to the usual behaviour of the non-annellated 1,2-dithiines, 6 displays no spontaneous sulfur extrusion under mild conditions, but only at high temperatures and in the presence of sulfur-binding agents, leading to the benzo[b]thieno-annellated thiophene 22. Moreover, 6 may be reduced to the dithiol 14 (or 13, respectively) and regenerated exclusively from this by oxidation. Further characteristic reactions of 6 are described (e.g. to the sulfoxide 18, to the pyridazine 19, and to the thiphosphoric ester 21).
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  • 56
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 445-445 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 57
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 449-455 
    ISSN: 0009-2940
    Keywords: Trifluoromethylsulfanyl compounds ; Pentafluorophenylsulfanyl compounds ; Trifluoromethylselenanyl compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tris(perfluoroorganochalkogenyl)methyl Compounds: Synthesis, Structures, and PropertiesReaction of (CF3S)2CHC(OC2H5)3 with CF3SCl or CF3SeCl in the presence of NaH in ether provides X(CF3S)2CC(O)OC2H5 (1a, b: X = CF3S, CF3Se). These compounds react with NH3 to form (CF3S)2CHC(O)NH2 (2b) which is also obtained from (CF3S)2CHC(O)OC2H5 and NH3. Dehydration of the amide 2b yields (CF3S)2CHCN (3b), which reacts with NaH and then with CF3SX (X = Cl, SCF3) or with RfCl (Rf = CF3Se, C6F5S) to give Rf (CF3S)2CCN [Rf = CF3S (3c), CF3Se (3d), C6F5S (3e)]. 3c is also obtained from (CF3S)3CBr and AgCN. Hydrolysis of 3c with conc. H2SO4 leads almost quantitatively to (CF3S)3CC(O)NH2 (2c), which on treatment with COCl2 gives only 3c and not the corresponding isocyanate. If phosgene is replaced by oxalyl chloride and treated with 2c in a 1:1 molar ratio, (CF3S)3CC(O)NCO (4a) is formed. The urea derivative (CF3S)3CC(O)NHC(O)NHC(O)C(SCF3)3 (4b) is obtained either by using a 2:1 molar ratio of 2c and [C(O)Cl]2 or from 2c and 4a. Attempts to substitute (CF3S)2CHCO2H - after treatment with NaH in ether - with CF3SCl provides low yields of 2,4-bis[bis(trifluoromethylsulfanyl)methylene]-1,3-dithietane (5). X-ray structure analyses are performed for (CF3S)3CCN (3c) and the 1,3-dithietane 5.
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  • 58
    ISSN: 0009-2940
    Keywords: 2-Pyridylalkylphosphanes ; Hemilabile ligands ; Nickel complexes ; Palladium complexes ; Platinum complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Coordination Chemistry of Hemilabile P,N-Hybride Ligands with Terminal 2-Pyridyl Donor Groups*P,N-hybride ligands 1-7 containing terminal 2-pyridyl donor groups have been obtained by base-catalyzed addition of diphenylvinylphosphane or 2-vinylpyridine to primary or secondary phosphanes [2-Py-(CH2)2-PR′H (R′ = H, Ph), HMeP-(CH2)3-PMeH] or by alkylation of organolithium phosphides, R2P-(CH2)3-PMeLi or 2-Py-(CH2)2-PR′Li (R = Ph, iPr; R′ = H, Ph), with 2-(2-chloroethyl)pyridine or di-tert-butylphosphetanium bromide. Upon reaction with NiBr2 3 H2O or K2MCl4 (M = Pd, Pt) the phosphanes (L) of type 2-Py-(CH2)2-P(R′)-(CH2)m-PR2 (1, 3, 6) form square planar Ni(II), Pd(II), and Pt(II) complexes of composition MX2(L) (10-14). With NiBr2 and K2MX4 the tripod type phosphane 2 forms square pyramidal complexes [MX(2)]X (M = Ni, Pd; X = Cl, Br; 15, 16). An X-ray structural analysis of [NiBr(2)]+Br- (15) reveals a distorted square pyramidal coordination geometry at Ni(II), the 2-Py donor being in apical position with a long Ni—N bond [2.270(15) Å]. The tetradentate ligand 7 forms Ni(II), Pd(II), and Pt(II) complexes MX2(7) which for M = Pd, Pt show dynamic behaviour by exchange of the terminal Py donor groups. With [RhCl(COD)]2 the tridentate ligands L (1 and 3) yield complexes of composition RhCl(L) (20, 21). The structure of 20 has been determinated by X-ray diffraction. The ligand 3, acting in a tridentate manner, is coordinated to Rh(I) in a distorted square-planar arrangement with a normal Rh—N distance [2.145(3) Å].
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  • 59
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    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 519-523 
    ISSN: 0009-2940
    Keywords: Calixarenes ; Friedel-Crafts reaction ; selective ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The para-acylation of calix[4]arene (2), calix[6]arene (3), and calix[8]arene (4) by Friedel-Crafts reaction with a wide variety of acyl chlorides leads to 5-7 in moderate to good yields. Friedel-Crafts reaction of 26,28-dimethoxycalix[4]arene (8) gave products 9 selectively disubstituted in the para-positions of phenol rings.
    Additional Material: 4 Tab.
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  • 60
    ISSN: 0009-2940
    Keywords: Copper(II) complexes, dinuclear ; Schiff bases, macrocyclic ; Redox properties ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexes with Macrocyclic Ligands, I. - Dinuclear Copper(II) Complexes with a Totally π-Conjugated Macrocycle of Schiff Base Type: Syntheses, Structures, Electro-, and Magnetochemical PropertiesThe dinuclear copper(II) complexes 6, 7, and 8 of three novel macrocyclic ligands were synthesized by the Schiff base condensation of 2 equiv. of 1,2-phenylenediamine and 2,6-diformylphenol in the presence of 2 equiv. of copper(II) perchlorate and were characterized by X-ray structure analyses, electrochemical investigations (DCV), and variable-temperature magnetic susceptibility measurements. Complex 6 exists in two different solvated crystalline forms. The Copper(II) ions in all three complexes are octahedrally coordinated with long axial distances to solvent molecules or perchlorate ions. The copper ions in 6 (in solvate a) are only five-coordinate and square-pyramidal. The CuIICuII complexes were reduced in successive, quasi-reversible, one-electron steps. The antiferromagnetic exchange interactions were determined. Upon dissolution in acetonitrile complex 8 decomposed to form [Cu(MeCN)4]+ClO-4 and the benzimidazolium percholorate 9 (X-ray structure determination).
    Additional Material: 9 Ill.
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  • 61
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 489-500 
    ISSN: 0009-2940
    Keywords: Alkenes ; Nickel complexes ; Stannenes ; Metal-metal bonds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: {Bis[bis(trimethylsilyl)methyl]stannio(II)}bis(η2-ethene)nickel(0) and Related Compounds, Part IIThe coordinatively unsaturated (16e) (ethene)nickel(0) stannylene complex (C2H4)2Ni=Sn{CH(SiMe3)2}2 (1) reacts with 1,6-heptadiene with preservation of the Ni=Sn bond to yield quantitatively the 1,6-diene derivative (η2,η2-C7H12)Ni=Sn-{CH(SiMe3)2}2 (2). The alkene ligands of both 1 and 2 are readily displaceable. Compounds 1 and 2 react with butadiene at -50°C by a 4-e oxidation of the metal-metal pair Ni(0)/Sn(II) to Ni(II)/Sn(IV) and concomitant reduction of two butadiene molecules to butenediyl moieties to afford stereo-selectively the 16-e complex Ni-cis-{η3(Ni),η1(Sn)-anti-C3H4CH2}2Sn{CH(SiMe3)2}2 (3). Similarly, the reaction of 1 or 2 with isoprene yields regio- and stereoselectively the derivative Ni-cis-{η3(Ni,η1(Sn)-anti-C3(3-Me)H3CH2}2Sn{CH-(SiMe3)2}2 (4). These reactions imply the cleavage of one formal Ni—Sn bond and the formation of two new Sn—C bonds. Upon reaction of 3 with PMe3 the configuration of the allyl system changes and, again fully stereoselectively, the 18-e addition compound (Me3P)Ni-cis-{η3(Ni),η1(Sn)-syn-C3H4-CH2}2Sn{CH(SiMe3)2}2 (5) is formed. When 5 is treated with BPh3, the phosphane ligand is trapped and, kinetically controlled, Ni-cis-{η3(Ni),η1(Sn)-syn-C3H4CH2}2Sn{CH(SiMe3)2}2 (6) is obtained as a stereoisomer of 3. At 40°C 6 slowly rearranges into the thermodynamically stable stereoisomer Ni-trans-{η3(Ni),η1(Sn)-syn-C3H4CH2}2Sn{CH(SiMe3)2}2 (7). Mild protolysis of 3 with pyridine hydrochloride or hydrobromide affords region and stereoselectively (Me3Si)2CH}2(X)SnNi-(η3-1-MeC3H4)(NC5H5) (X = C1, 8a; Br, 8b). In the course of this protonation reaction one butadiene molecule is eliminated, accompanied by a 2-e reduction of the metal-metal pair Ni(II)/Sn(IV) to Ni(II)/Sn(II) and, at the expense of two Sn—C bonds, reformation of a Ni—Sn bond. All compounds are isolated in high yield and fully characterized by 1H-, 13C-, and 31P-NMR spectroscopy.
    Additional Material: 3 Tab.
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  • 62
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 533-539 
    ISSN: 0009-2940
    Keywords: Bissulfenyl chlorides ; fluoro substituted ; 1,3-Dithioles ; 1,3,2-Dithiazoles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Halogen-Carbon-Sulfur Compounds: Syntheses with 1,1,1,4,4,4-Hexafluoro-2-butene-2,3-bissulfenyl ChlorideThe bifunctional bissulfenyl chloride 3 is obtained by chlorination of the dithiete 1 or tetrathiocine 2. By excessive chlorination the saturated bissulfenyl chloride 4 is formed. 3 reacts with primary amines to yield the 1,3,2-dithiazoles 5a-e, whereas by reactions with active methylene compounds like ketones or β-dicarbonyls the compounds 7-14 are obtained with HCl elimination. 13 as well as 14 are converted into the carboxylic acid 15 from which the 1,3-dithiole 17 is obtained by decarboxylation. 3 reacts with disulfene to form tetrakis-(trifluoromethyl)tetrathiafulvalene as well as 4,4′,5,5′-tetrakis(trifluoromethyl)-2,2′-spirobi[1,3-dithiole] (18), whose crystal structure has been determined.
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  • 63
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 959-963 
    ISSN: 0009-2940
    Keywords: Rearrangements, thermal ; Propargyl-Cope reaction ; 1,5-Hexadiyne-3,4-diol ; Cyclobutene ; 3,4-diacetyl ; Fragmentations, retro-ene ; Tandem reactions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal behavior of meso- and d,1-3,4-dimethyl-1,5-hexadiyne-3,4-diol (meso- and d,1-4) has been studied at 400°C in the gas phase. In a tandem reaction the diols isomerize via the bisallenes 5 first to cis- and trans-3,4-diacetylcyclobutene (cis- and trans-8) which have been detected as intermediates by 13C-NMR spectroscopy as well as catalytic hydrogenation to 1,2-diacetylcyclobutane (9). Subsequently, 8 stabilizes itself by ring opening to (E,Z)- and (E,E)-3,5-octa-dien-2,7-dione (E,Z) and [(E,Z)-6]. As a side reaction retroene cleavage of 4 to 2-butynone (10) and methyl vinyl ketone (12) is observed. By pyrolysis of the pure diastereomers 4 it is shown that the retro-ene process is more pronounced in the d,l than in the meso series.
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  • 64
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2373-2379 
    ISSN: 0009-2940
    Keywords: Chelating ligands ; Molybdenum complexes ; Peroxo complexes ; Catalysis ; Olefine epoxidation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Substituted N,N-Chelate Ligands - Applications in Molybdenum-Catalyzed Epoxidation of Olefins*Oxodiperoxomolybdenum complexes 4 of substituted 2-[3(5)-pyrazolyl]pyridines (2a-g) were synthesized in order to control the solubility of these complexes in organic solvents. Alkyl side chains (butyl, octyl, octadecyl) increase the solubility of the complexes and enable spectroscopic investigations in solution. Due to the symmetry of the ligands the peroxo complexes 4 appear in two isomeric forms, with the terminal oxo ligand in the trans position either to pyridine or to pyrazole. The latter isomer of (C5H4NC3H2N2CH2COOEt)MoO(O2)2 (4f) was characterized by an X-ray structure analysis. The alkyl-substituted peroxo complexes are active catalysts for the epoxidation of olefins with tert-butyl hydroperoxide.
    Additional Material: 2 Ill.
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  • 65
    ISSN: 0009-2940
    Keywords: Manganese complexes ; Insertion processes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mn(NO)2L2H complexes [L = PMe3 1a, PEt3 1b, P(OMe)3 1c, P(OEt)3 1d, P(OiPr)3 1e] have been prepared by the reaction of the corresponding Mn(NO)2L2Br compounds with NaBH4 in ethanol. The reactivity of 1a and 1b is compared to that of Mn(CO)3L2H species (L = PMe3 2a, L = PEt3 2b). Compound 1b reacts with weak acids like PhOH, (CF3)2CHOH and CH3COOH to yield Mn(NO)2(PEt3)2X complexes [X = OPh 3a, OCH(CF3)2 3b, OC(O)CH3 3c] and H2. Compound 2b does not undergo reaction with these acids. At room temperature in toluene 1a, b undergo facile CO2 insertion processes, while 2a, b do not show this reactivity even under more rigorous reaction conditions. From 1a, b and CO2 formato complexes Mn(NO)2L2[OC(O)H] (L = PMe3 4a, L = PEt3 4c) are obtained. The reaction of 1b with salicylaldehyde in toluene proceeds with the formation of a [2-(hydroxymethyl)-phenoxy]dinitrosylbis(triethylphosphane) manganese complex 5b, which exchanges the phenoxy ligand in the presence of excess of salicylaldehyde to give (2-formylphenoxy)-dinitrosylbis(triethylphosphane)manganese (6b) and α,2-dihydroxytoluene. p-Hydroxybenzaldehyde, vanilline, and 4-hydroxy-3,5-dimethoxybenzaldehyde and 1b also afford phenoxy derivatives Mn(NO)2(PEt3)2(OAr) [Ar = p-OC6H4-CHO 7a; OC6H3-2-OCH3-4-CHO 7b; OC6H2-2,6-(OCH3)2-4-CHO 7c] and H2. Compounds 2a, b do not react with any of these hydroxybenzaldehydes. Compounds 1a, b have been converted into Mn(NO)2L2 [(Z)-C(COOR′)≡C(R)H] species (L = PMe3, R = H, R′ = Me 8a; L = PEt3, R = H, R′ = Me 8b; L = PMe3 R, R′ = Me 9a; L = PMe3, R = Ph, R′ = Et 10a; L = PMe3, R = COOMe, R′ = Me 11a; L = PEt3, R = COOMe, R′ = Me 11b) in the presence of alkyl propiolates RC≡CCOOMe (R = H, Me, Ph, COOMe; R′ = Me, Et). Similarly, but under more rigorous conditions, insertion of RC≡CCOOMe (R = H, COOMe) into 2a, b occurs and α metalation products Mn(CO)3(PMe3)2[(Z)-C(COOMe) = CHR] (L = PMe3, R = H 12a; L = PEt3, R = H 12b; L = PMe3, R = COOMe 13a; L = PEt3, R = COOMe 13b) are formed. In the case of the methyl propiolate insertion into 2a, 10% of an additional β-metalation compound Mn(CO)3(PMe3)2[(Z)-CH = CH(COOMe)] (12c) have been detected spectroscopically. Compounds 11b and 13a, b have been transformed into manganacyclic complexes MN[C(COOMe)=CH(COOMe)]-(NO)2(PEt3)2 (14b) and MN[C(COOMe)=CH(COOMe)]-(CO)2L2 (L = PMe3 15a; L = PEt3, CO 15b; L = PEt3 15c). Compound 15c has been identified spectroscopically, and 1a, 8a, and 9a have been characterized by X-ray structure determinations.
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  • 66
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2483-2488 
    ISSN: 0009-2940
    Keywords: vic-Dioximes ; N2O2 macrocycles ; Trinuclear complexes ; Pentanuclear complexation ; Tribenzo[b.h.l][1,10,4,7]dioxadiazacyclotetradecine derivatives ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new vic-dioxime ligand 2 (LH4) carrying a 14-membered N2O2 macrocycle has been prepared. Mononuclear complex (LH3)2Ni, trinuclear complexes (LH)2Cu3, (LH)2Co3, (LH)2-Pd3, and (LH)2Co3(py)3Cl3, dinuclear complex (LH3)2-(UO2)2(OH)2, and pentanuclear complex [L2Cu5(phen)2]-(NO3)2 have been synthesized from LH4. The electrochemical properties of tri- and pentanuclear complexes were investigated by cyclic voltammetry. For (LH)2Cu3 two reduction waves appeared at 0.215 and -0.870 V. [L2Cu5(phen)2](NO3)2 exhibited four reduction waves at 0.200, -0.025, -0.670, and -1.170 V.
    Additional Material: 5 Ill.
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  • 67
    ISSN: 0009-2940
    Keywords: Uncharged auxiliary bases ; Triaminoiminophosphorane bases ; Deprotonation ; Hindered bases ; Polymeric bases ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and properties of a number of very strong iminophosphorane bases up to an extremely high level of steric hindrance are described. They cover a range of ca. 4 pK units in basicity and a range of more than 11 orders of magnitude in their rates of methylation with methyl iodide. Most of the systems are readily prepared in up to molar quantities, conveniently recovered from their salts and are of high chemical and thermal stability. Crystal structures were determined in order to parametrize a force field, which is utilized in molecular modeling studies offering a rationalization of the observed differences in steric hindrance and basicity. Depending on the degree of steric protection of the basic center, these novel bases are proposed as unprecedented, versatile auxiliary bases in E2 eliminations and in reactions involving deprotonation in the presence of more or less strong electrophiles.
    Additional Material: 8 Ill.
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  • 68
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1349-1353 
    ISSN: 0009-2940
    Keywords: Isophosphaalkynes ; Transition metal complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Transition-Metal-Substituted Acylphosphanes and Phosphaalkenes, XXI.  -  Isophosphaalkynes as μ3-Ligands in Transition Metal ComplexesReaction of the μ-isophosphaalkyne complex (η5-C5H5)2 (CO)2(μ-CO)Fe2(μ-CPMes) (Mes = 2,4,6-Me3C6H2) (2a) with [(Z)-Cyclooctene]Cr(CO)5 or Fe2(CO)9 gives rise to the μ3-isophosphaalkyne complexes (η5-C5H5)2(CO)2(μ-CO)Fe2{μ-CP[M(CO)n]Mes} 3a [M(CO)n = Cr(CO)5] and 4a [M(CO)n = Fe(CO)4]. Similarly (η5-C5H5)2(CO)2(μ-CO)Fe2{μ-CP[Cr (CO)5]C6H2(CF3)3-2,4,6} (3d) is obtained. The metal carbonyl fragments are attached to 2 in a η1-fashion by the lone-pair at the phosphorus. In contrast to this the treatment of 2a with (Ph3P)2Pt(η2-C2H4) affords complex 5a in which 2a serves as an η3-3e ligand towards the PtPPh3 moiety. The molecular structures of 3a and 5a are determined by single-crystal X-ray analysis.
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  • 69
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1355-1357 
    ISSN: 0009-2940
    Keywords: Diphosphanylhydrazides ; Diphosphanes, dinitrogen-bridged ; Cycloplatinaphosphahydrazides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: While the transition metal complexes of bis(phosphanyl)amines (PII-N-PIII) have been known for over three decades, the ligating properties of the next homologue PIII-N-N-PIII have been unprecedented so far. The X-ray structures of cycloplatinaphosphanehydrazides, [(OR)2PN(Me)N(Me)P(OR)2-PtCl2], reveal short distances for the P-N [1.639(5) Å] bonds.
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  • 70
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1359-1362 
    ISSN: 0009-2940
    Keywords: Silanes ; Siloxanes ; Si - C bond, selective cleavage ; Arylsilylmethanes ; Si,C,O single-source CVD precursor ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A synthetic route to partly silylated tetra(silyl)methanes (ArH2Si)nC(SiH3)4  -  n′ to their precursors (TfH2Si)nC-(SiH2Ar)4  -  n (Ar = p-tolyl, phenyl; Tf = CF3SO3; n = 3, 2, 1), and to 1,3-bis(trisilylmethyl)disiloxane [(H3Si)3CSiH2]2O (9) is reported. Starting from symmetrical tetrakis(arylsilyl)-methanes (aryl = p-tolyl, phenyl), we have obtained the selectively dearylated (arylsilyl)silylmethanes (ArH2Si)nC(SiH3)4  -  n (Ar = p-tolyl, phenyl; n = 3, 2, 1) by Si - Ar cleavage with equivalent quantities of trifluoromethanesulfonic acid (triflic acid) and hydrogenation of the corresponding silyl triflates (TfH2Si)nC(SiH2Ar)4  -  n (n = 3, 2, 1) with LiAlH4. The synthesis of 9 has been accomplished by treating trisilyl(p-tolylsilyl)methane p-TolH2SiC(SiH3)3 (7) with stoichiometric amounts of triflic acid to give (trisilylmethyl)silyl triflate TfH2SiC(SiH3)3 (8) and hydrolysing the latter with water.
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  • 71
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1363-1368 
    ISSN: 0009-2940
    Keywords: 1,2-Diboroles, 2,5-dihydro- ; 1,3-Diboroles, 2,3-dihydro- ; Cobalt complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A New Approach to 1,2- and 1,3-DiboroleHerrn Prof. Dr. Joachim Knappe zum 65. Geburtstag gewidmet.Diaminoborylation of 1,3-dilithiopropenes leads to the (Z)-1,3-bis(diaminoboryl)propenes 4a, b, which are transformed by an amine/chlorine exchange to the (Z)-1,3-bis(aminochloroboryl)propenes 5a, b. These react with sodium to yield the 2,5-dihydro-1H-1,2-diboroles 2c, d, whereas the reaction with potassium leads to the 2,3-dihydro-1H-1,3-diboroles 6a, b by rearrangement of the C3B2 skeleton. The constitutions of the heterocycles 2c, d and 6a, b are established by X-ray structure analyses. Reaction of the 1,2-diboroles 2c, d with (C5H5)Co(C2H4)2 leads to the red (1-borabutadiene)cobalt complexes 3c, d. In 3c a sigmatropic rearrangement is studied by NMR spectroscopy.
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  • 72
    ISSN: 0009-2940
    Keywords: Tungsten complexes ; Rhenium complexes ; Iron complexes ; Ruthenium complexes ; Osmium complexes ; Cobalt complexes ; Vinyl ; Cyclohexadienyl ; Cycloheptadienyl ; Cyclooctatrienyl ; Hydrocarbon-bridged complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrocarbon-Bridged Complexes, XXX.  -  Nucleophilic Addition of Carbonylmetallates to Cationic Vinyl, Diene, Dienyl and Triene Complexes of Iron, Ruthenium and Cobalt: Di-, Tri-, Tetra- and Pentametallic Complexes with σ,σ- and σ,π-Hydrocarbon BridgesHerrn Professor Ekkehard Lindner zum 60. Geburtstag gewidmet.The reactions of [Re(CO)5]-, [Ru(CO)2Cp]-, and [Os(CO)4]2- with [Cp2(OC)2Fe2(μ-CO)(μ-η1:η2-CH=CH2)]+, [Cp*Ru(η2:η4-1,3,7-octatriene)]+, [(OC)Fe(η4-diene)(η5-cycloheptadienyl)]+, and [CpCo(η5-cyclodienyl)]+ give the nucleophilic adducts whereas with [Mn(CO)5]-, [W(CO)3Cp]-, and [Fe(CO)2Cp]- formation of the corresponding C-C coupling products and of the metal-metal-bonded dimers is observed. The structures of Cp*Ru(μ-η1:η2:η3-1,5-octadienyl)Re(CO)5 (4), [Cp* Ru(μ-η1:η2:η3-1,5-octadienyl)]2Os(CO)4 (6), and of (OC)-Fe(η4-1,3-cyclohexadiene) (μ-η1:η4-1,3-cycloheptadiene)Re(CO)5 (9) have been determined by X-ray diffraction.
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  • 73
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1379-1385 
    ISSN: 0009-2940
    Keywords: Hydrotris(triazolyl)borate ; metal complexes ; Chelate ligands ; Clathrates ; Magnetochemistry ; Spin crossover ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The bis[hydrotris(1,2,4-triazolyl)borate]metal complexes [M{HB(C2H2N3)3}2] with M = Fe (5), Co (6), Cu (7), Zn (8) are obtained from MX2 and K[HB(C2H2N3)3] (9). The complexes are characterized by IR, UV/Vis, and MS. Temperature-variable magnetic measurements show a Curie-Weiss behavior for the paramagnetic complexes 6 and 7 with a temperature-dependent magnetic moment for 6. The iron complex 5 exhibits a spin crossover from diamagnetic to paramagnetic, starting at around 270 K. Single-crystal X-ray structures of the solvates 7 · 4 CH3OH and 9 · 2 H2O have been determined. The structure of 7 · 4 CH3OH shows the Jahn-Teller distorted copper complex 7 surrounded by methanol molecules through hydrogen bonding to exocyclic nitrogen atoms of the tris(1,2,4-triazolyl)borate ligand. The crystal system for 7 · 4 CH3OH is monoclinic, space group P21/n. Compound 9 · 2 H2O is a one-dimensional coordination polymer with the potassium atom bridged by the water molecules and the tris(1,2,4-triazolyl)borate ligand and crystallizes in the orthorhombic space group Ccm21.
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  • 74
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1489-1493 
    ISSN: 0009-2940
    Keywords: Conjugate alkylation ; Trimethylaluminium ; Copper catalysis ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conjugate methylation of α,β-unsaturated ketones with trimethylaluminium occurs smoothly in a very simple procedure under the catalytic effect of Cu1 salts. Scope and limitations of this process as well as the influence of solvent and catalyst on the kinetics were studied. In addition, the effect of chlorotrimethylsilane as an additive was investigated. Attack on the carbonyl group in 1,2-fashion could not be observed under the reaction conditions.
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  • 75
    ISSN: 0009-2940
    Keywords: 1,2,3,4-Tetrazines ; 2H-Cyclopenta[e]-1,2,3,4-tetrazines ; Azodiazo-tetrazino isomerism ; Ketene imines ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 2-aryl-2H-cyclopenta[e]-1,2,3,4-tetrazines 3a-n are formed by coupling of the diazocyclopentadienes 1a and 1b with arenediazonium salts and subsequent reversible electrocyclization of the primary coupling products 2a-n. From the solutions of the equilibrium mixtures of 2a ⇌ 3a - 2n ⇌ 3n the tetrazines 3a-d, h-k and the arylazo-diazocyclopentadienes 2e-g and 21-n crystallize. The 2-methyl-2H-cyclopenta[e]-1,2,3,4-tetrazines 3o and 3p are obtained by addition of methyllithium to 1a and 1b followed by a diazo transfer reaction and cyclization. In solutions of 3o and 3p the ring-opened isomers 2o and 2p could not be detected. X-ray analyses of 3h and 3p prove their bicyclic planar geometry in the solid state. 15N-NMR and temperature-dependent 1H-NMR spectroscopy have enabled a detailed study of the reversible ring closure reaction in the case of 2d ⇌ 3d. Reaction of 2-phenyl-2H-cyclopenta[e]-1,2,3,4-tetrazine (3b) with tetrafluoroboric acid results in the formation of the protonated monocyclic salt 4. Furthermore 3b undergoes electrophilic substitution reactions preferably at C-7, as demonstrated by bromination, formylation, and trifluoroacetylation. Photolysis of solutions of 2i/3i, 2k/3k, and 21/31 leads to the ketene imines 11a-c. The structure of 11c has been determined by X-ray crystallography.
    Additional Material: 4 Ill.
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  • 76
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1627-1632 
    ISSN: 0009-2940
    Keywords: Triarylmethane dye ethynylogues ; Trifluoromethyl group ; Triphenylmethane dyes ; Photostability ; Absorption spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Triarylmethane dye ethynylogues 7′- 11′ containing trifluoromethyl group(s) are synthesized in moderate to good yields by treating 1,1,3-triaryl-2-propyn-1-ols, prepared from diaryl ketones and lithium arylacetylides bearing trifluoromethyl group(s), with perchloric acid. The first absorption bands of a series of triarylmethane dye ethynylogues containing trifluoromethyl group(s) 11′ are observed around 700 nm. The photostability of the triarylmethane dyes is also examined.
    Additional Material: 4 Ill.
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  • 77
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1699-1706 
    ISSN: 0009-2940
    Keywords: Aziridines, 2-imino-, chiral, non-racemic ; Imidoyl halides, 2-halo ; Imidates, 2-chloro ; 1,3,2-Thiazaphos-pholidines ; Amidines, 2-halo ; 1,3-Elimination, inversion of configuration in ; E/Z Diastereomerization ; [2 + 1] Cycloreversion, kinetics of thermal ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 2-halo imidoyl chlorides 7 are obtained from the amide 5 and the 2-halo amides 6 by the action of phosphorus pentachloride and thionyl chloride, respectively. Non-racemic (S)-6a is converted into 7a which is racemic, however. The reaction of Lawesson's reagent with 6a furnishes the diaste-reomeric 1,3,2-thiazaphospholidine derivatives 15. Treatment of (S)-6a (98% ee) with methyl triflate affords 2-chloro imidate 8 (95% ee) which reacts with methanamine in the presence of methanammonium chloride to yield the 2-chloro amidine (S)-9a (90% ee). The 2-halo imidoyl halides 7a and b react with methanamine to produce the 2-halo amidines 9a and b.  -  Strong bases, e.g. potassium tert-butoxide or sodium hydride in the presence of catalytic amounts of tert-butyl alcohol, eliminate hydrogen chloride or bromide from the 2-halo amidines 9a and b and (S)-9ato yield mixtures of the 2-iminoaziridines (E)- and (Z)-4, and (E,R)- and (Z,R)-4 (83% ee), respectively. The 1,3-elimination of hydrogen bromide from 9b is diastereoselective at -30 to -40° [(E)-4:(Z)-4 = 〈10:〉90]. The diastereomers equilibrate at 36° with (kEZ + kZE) = (5.92 ± 0.08) . 10-5 s-1 (K = kEZ/kZE = 0.428 ± 0.013). - The thermolysis of (E)- and (Z)-4 in [D6]benzene solution yields the imine 16 and methyl isocyanide (17). The decomposition follows the first-order rate law. The following Arrhenius and Eyring parameters are calculated from five rate constants obtained in the temperature range of 70-110°: Ea = (115.2 ± 0.4) kJmol-1, IgA = (12.06 ± 0.28), δH
    Additional Material: 2 Ill.
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  • 78
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1729-1733 
    ISSN: 0009-2940
    Keywords: Pyrazoles ; Aminyls, heterocyclic ; Pyrazolo[1,5-a]benzimidazoles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Free Radical Reactions of N-Heterocyclic Compounds, XIV[1]. - Oxidative Cyclization of Anilinopyrazoles to Pyrazolo[1,5-a]benzimidazolesHerrn Professor Christoph Rüchardt zum 65. Geburtstag gewidmet.Substituted Anilinopyrazoles 1 were oxidized by dibenzoyl peroxide or lead(IV) oxide. Different oxidation products were isolated depending on the substituents in the anilino group of anilinopyrazoles 1. Intermediate pyrazolyl radicals 5, which could be trapped by triphenylmethyl or phenoxyl radicals, undergo cyclization reaction with formation of pyrazolo[1,5-a]benzimidazoles 4. The structures of compounds 4 were proven by 1H- and 13C-NMR spectroscopy, 15N labeling and transformation of 4e to the betain 7e.
    Additional Material: 2 Tab.
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  • 79
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1735-1745 
    ISSN: 0009-2940
    Keywords: [18]Annulenes ; Liquid crystals, discotic ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Triphenanthro-Anellated [18]Annulenes with Alkoxy Side Chains - A Novel Class of Discotic Liquid CrystalsTwo different types 6 and 16 of [18]annulenes condensed with phenanthrene systems were prepared by cyclocondensation reactions (Schemes 2 and 3). The central 18-membered rings do not show a macrocyclic diamagnetic ring current. Conformational analyses and X-ray analyses in the solid state reveal non-planar structures in which aromatic “islands” are connected by (E)-configurated olefinic bridges. The introduction of long alkoxy side chains yields a new class of discotic liquid crystals; either ND or hexagonal columnar phases are generated, which were characterized by DSC, microscopy with polarized light, and small-angle scanning X-ray.
    Additional Material: 4 Ill.
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  • 80
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1761-1764 
    ISSN: 0009-2940
    Keywords: Mannich reaction ; α-Aminoalkylation ; Ketene acetals, O-silylated ; Amino nitriles ; Diastereoselectivity ; Ik Addition ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: LiClO4 Induced One Pot Three-Component Aminoalkylation of AldehydesLiClO4-mediated one-pot reaction of isobutyraldehyde (1) or benzaldehyde (5) with (trimethylsilyl)dialkylamines 2 and C nucleophiles such as O-silylated ketene acetals 3, 6, allyl Grignard, lithium (trimethylsilyl)acetylide, triinethylsilyl cyanide, and diethylzinc afforded in high yields the corresponding aminoalkylation products 4 and 7-13. The lithium enolate of cyclohexanone adds in 5 M LiClO4 solution in an Ik manner to the corresponding mannich base (19, 20) with good yield.
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  • 81
    ISSN: 0009-2940
    Keywords: Anthracenes ; Oxyallyl cations ; Ketones, α,α'-oligobromo- ; Dibenzohomobarrelenes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sonication of a zinc/copper couple, N,O-bis(trimethylsilyl)-acetamide (BSA) and α,α'-oligobromo ketones in benzene gives rise to oxyallyl intermediates which cycloadd to anthracene. Starting from 1,1,3,3-tetrabromoacetone (2a) and anthracene (1a), we obtained 11,11,13-tribrominated adduct 4 as the major product (42%). The expected 11,13-dibrominated adduct trans-3 was formed as a minor product (5%), but it became the main product when the known oxyallyl methodology was applied. Dibenzohomobarrelenes 9 and 17 were prepared by short routes.
    Additional Material: 1 Tab.
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  • 82
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1747-1753 
    ISSN: 0009-2940
    Keywords: Isomerization, thermal ; Radicals ; D-Labeling ; 1,5-Hexadiyne ; Pentafulvene ; Rearrangement, homoallyl ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal Rearrangements, XXIII[1].  -  The Thermogram of a C6H6 Chemistry in the Temperature Range from 450 to 730°CThe thermal isomerization of 1,5-hexadiyne (1) and its [1,6-D2]-labeled derivative (1a) was studied in the temperature range 450-730°C and in the presence of different carrier gases (N2, H2, D2, N2/toluene). By detailed analysis (GC, GC MS, NMR) all volatile reaction products were identified and determined quantitatively by using hexafluorobenzene as an internal standard. The experimental data show clearly that the reaction products are formed by two different routes: (i) electrocyclization leading to dimethylene cyclobutene (3) at temperatures up to about 600°C and (ii) radical reaction leading to benzene (4) and pentafulvene (5) at temperatures above 550°C. Cyclopentadienylmethyl radicals are supposed to be the essential radical intermediates.
    Additional Material: 2 Ill.
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  • 83
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1765-1779 
    ISSN: 0009-2940
    Keywords: Diradicals ; NO and O2 trapping ; Heat of formation ; Energy well ; Rearrangments ; Bergman cyclisation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Energy Well of Diradicals, V[1].  -  1,3,5-Cyclohexatriene-1,4-diyl and 2,4-Cyclohexadiene-1,4-diylThe energy profile of the Bergman rearrangement of (Z)-3-hexene-1,5-diyne (4) has been established from the NO and oxygen dependance of the trapping rate of the intermediate diradical 1 which leads to a heat of formation for 1,4-didehy-drobenzene (1) of δHOf= 138.0 ± 1.0 kcal . morl-1. By the same technique the heat of formation of 1,2,4-cyclohexatriene (2), generated by thermolysis of (Z)-1,3-hexadien-5-yne (10), gives δHOf = 105.1 ± 1.0 kcal . mol-1 which indicates a high diradical character for 2.
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  • 84
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1797-1798 
    ISSN: 0009-2940
    Keywords: Titanocenes ; Fulvenes ; Solvent effect ; Ketyls ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Reaction of Bis(trimethylphosphane)titanocene with KetonesFulvenes are the products of the reaction of aliphatic and aromatic ketones with bis(trimethylphosphane)titanocene in nonpolar solvents, but no formation of pinacols is observed. The mechanism is discussed.
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  • 85
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1781-1795 
    ISSN: 0009-2940
    Keywords: Resonance energy ; Stabilisation energy ; Propargyl resonance ; Force field calculation ; Intrinsic rotational barrier ; Single pulse shock tube ; Gasphase kinetics ; Heats of hydrogenation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Propargyl Stabilisation EnergyFor the alkynyl-substituted olefines 1-14 activation parameters for the geometrical isomerisation have been determined in the gasphase by the single-pulse shoke-tube technique. By comparison of these barriers with the corresponding one of the isolated double bonds, each corrected by the steric energy contribution of the ground and transition state, a value of 7.8 ± 1.3 kcal · mol-1 for the propargyl stabilisation energy (PrSE) has been derived.
    Additional Material: 11 Tab.
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  • 86
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1799-1802 
    ISSN: 0009-2940
    Keywords: as-Triazinium salt, fused ; Ring opening ; Ring transformation Heteroaromaticity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ring transformation of the tricyclic furo-fused as-triazinium salt 1 in the presence of nucleophilic reagents (e.g. sodium hydrogensulfide, sodium salts of malonic ester, ethyl cyanoacetate, acetylacetone, dimedone, or malononitrile) leads to the two new heteroaromatic ring systems thieno[2,3-e]pyrido[1,2-b]-as-triazinium salt (5) and differently substituted cyclopenta[e]pyrido[1,2-b]-as-triazine compounds (8, 9, 10, 11, and 13).
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  • 87
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1803-1806 
    ISSN: 0009-2940
    Keywords: Singlet carbenes ; [4 + 1] Cycloadditions ; 1,2,4,5-Tetrazines ; SEAr reactions, intramolecular ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Wanzlick Carbenes in the [4 + 1] Cycloaddition Reaction with Bis(methylthio)- and Bis(trifluoromethyl)-1,2,4,5-tetrazineThe 3,6-disubstituted 1,2,4,5-tetrazines 3 and 4 have been submitted to a [4 + 1] cycloaddition reaction with the nucleophilic singlet carbenes (Wanzlick carbenes) 2a-d, which are generated from the precursors 1a-d. With 3 as diazadiene the expected spiro compounds 6a-d are formed. In contrast to this presumed two-step reaction sequence of 3, with the tetrazine 4 the cascade cycloaddition/cycloelimination is surprisingly followed by an intramolecular electrophilic aromatic substitution to yield the chiral tetracyclic compounds of type 8 with high diastereoselectivity. The crystal structure of 8d has been determined by X-ray diffraction methods.
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  • 88
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A-105 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 89
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1811-1813 
    ISSN: 0009-2940
    Keywords: Vinylferrocene ; Palladium-catalyzed couplin ; (Ferrocenylvinyl)arenes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (Ferrocenylvinyl)arenes 3, 5, and 7 are obtained from vinylferrocene (1) and substituted aromatic and heteroaromatic halides by palladium-catalyzed Heck-type reactions. Up to three ferrocene units are introduced in one step by the multi-fold reaction of 1,2-dibromo- (4) or 1,3,5-tribromobenzene (6) with 1. The first crystal structure of a bis(ferrocenylvinyl)benzene chromophore (5) is reported.
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  • 90
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1807-1810 
    ISSN: 0009-2940
    Keywords: Gas-phase organometallic chemistry ; Bond activation, C-H, C-C ; Coupling reactions, C-C ; Lanthanide cations ; Benzene complexes ; Butadiene complexes ; FT MS ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cationic butadiene and benzene complexes CeC4H6+ and CeC6H6+ are the main products in the reaction of thermalized Ce+ ions with propene in the gas phase, as shown by FT MS. Following the formation of the primary products, i.e. CeCH2+ and CeC3H4+, selective C-C coupling processes at the lanthanide cation occur as secondary reactions with high efficiency. Ligand-exchange reactions and comparative collision-induced dissociation experiments are applied to probe the structures of the final reaction products of this first example of Ce+ gas-phase chemistry. The reaction of Ce+ with cyclopropane yields a product distribution very similar to the propene reaction; however, it reacts significantly slower. Furthermore, La+ reacts in nearly the same manner with propene as Ce+ which indicates that the single f electron in the latter ion is chemically inert.
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  • 91
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    Berichte der deutschen chemischen Gesellschaft 127 (1994) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 92
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1837-1842 
    ISSN: 0009-2940
    Keywords: Tripod ligand synthesis ; Oxetane cleavage ; Phosphane-Boranes ; Chiral neopentyl system ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chiral Tripod Ligands: A New Synthetic Route to Chiral C1-symmetrical Neopentyltris(phosphane) Ligands H3CC[CH2P(Ra)2][CH2P(Rb)2][CH2P(Rc)2]A novel synthesis of chiral tripod ligands H3CC[CH2P-(Ra)2][CH2P(Rb)2][CH2P(Rc)2] (6) containing three different donor groups at their neopentyl backbone is described. The key intermediates H3CC[CH2P(Ra)2][CH2P(Rb)2](CH2OH) (3) are easily obtained starting from pentaglycerine, H3CC-(CH2OH)3, via the oxetanes (2) following published procedures. The compounds 3, after protection of the phosphane functions by BH3 {formation of H3CC[CH2P(Ra)2BH3][CH2P(Rb)2BH3](CH20H) (4)} are transformed into the mesylates H3CC[CH2P(Ra)2BH3][CH2P-(RB)2BH3](CH20Ms) (5), which upon reaction with KP(Rc)2 and deprotection with morpholine gives fair yields of racemic 6. The synthetic route described is thus a valuable and efficient alternative to a recently published procedure, based on H3CC(CH2CI)(CH2Br)(CH20S02CF3) as the key intermediate. The compounds 2-6 are obtained in analytically pure form and are fully characterised by spectroscopic data.
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  • 93
    ISSN: 0009-2940
    Keywords: Metal(II) complexes mono- and dinuclear ; Schiff bases, macrocyclic ; Redox properties ; Superexchange interactions of d9 systems ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexes with Macrocyclic Ligands, III[1]. - Mono- and Dinuclear Macrocyclic Transition Metal Complexes of Ligands of Schiff Base Type: Syntheses, Structures, Electro- and Magnetochemical Properties.Four new mononuclear metal(II) complexes (4a-d) of a macrocyclic ligand derived from the Schiff base condensation of 2 equiv. of 1,2-phenylenediamine (3a) and 5-tert-butyl-2-hydroxy-1,3-benzenedicarbaldehyde (2) were synthesized and the cobalt complex 4b characterized by X-ray structure analysis. Reaction of 1,2-diamino-3,4,5,6-tetrafluorobenzene (3b) with the dicarbaldehyde 2 in the presence of Mn(ClO4)2 or Co(ClO4)2 leads to the novel metal-free macrocyce 6 (X-ray structure determination). The macrocycle 6 and Cu(ClO4)2 yield the new dinuclear copper complex 8, the structure of which was also determined by X-ray diffraction. The copper-(II) ions in 8 have a distorted square-pyramidal coordination by the four donor atoms of the macrocycle and an apical acetonitrile ligand. The Cu…Cu distance is 318.1 pm, and the two Cu(II) ions show only a small antiferromagnetic exchange interaction of J= -41 cm-1. Another new dinuclear Cu(II) complex (10) of a macrocyclic ligand derived from the Schiff base condensation of 2,2′-diaminooctafluorobiphenyl (9) and dicarbaldehyde 2 was synthesized and characterized by X-ray structure analysis, electrochemical investigations (DCV), and variable-temperature magnetic susceptibility measurements. One copper ion in complex 10 is five-coordinate (square-pyramidal), the other one six-coordinate (distorted octahedral). The Cu…Cu distance is 301.5 pm and the antiferromagnetic coupling J= -774 cm-1.
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1843-1849 
    ISSN: 0009-2940
    Keywords: Amine-Diboroxanes, bicyclic ; 1,2-Deaminoboration, intramolecular ; Deoxyboration ; Allyl-aminoboranes, organosubstituted, rearrangement ; C-Borylation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Rearrangement and Degradation of Bicyclic Amine-Tetraalkyldiboroxanes[1]The amine-tetraalkyldiboroxanes [1a: R1,4,7,7′ = Et; 1b: R1,4,7 = Et, R7′ = Ph; 1b′: R4,7,7′ = Et,R1 = Ph; 1c: R1,7,7′ = Et, R4 = Ph] react on heating by EtBO elimination and allylborane rearrangement to yield the allyl-aminoboranes Me2NB(Et)CH2C(R4)=C(R7,7′) [2a: R4,7,7′ = Et; 2b/2b′: R4 = Et, R7,7′ = Et, Ph; 2c: R4 = Ph, R7,7′ = Et]: On heating above 60°C the diastereomeric syn/anti-Id/1d′(Id: R1,7 = C8H14, R4,7′ = Et; 1d′: R1,7′ = C8H14, R4,7 = Et) give the unsaturated rac-amino-trialkyldiboroxane (rac-3) (X-ray structure analysis) by intramolecular 1,2-deaminoboration. rac-3 is characterized by reaction with (Et2BH)2 and (Et2BD)2 with formation of the 1,2,6-oxadiborinane 5 by evolution of H2 or HD respectively. The intramolecular CH-borylation of rac-3 is compared with those of the thujopsen hydrocarbons I-III.
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    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1827-1835 
    ISSN: 0009-2940
    Keywords: Imido complexes, organometallic ; Molybdenum complexes ; Tungsten complexes ; Alkene complexes ; Alkyne complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Highervalent Derivatives of the d-Metal Acids, 14[1].  -  Diimido Complexes [M(NR)2(PMe3)2(L)] of Tetravalent Molybedenum and Tungsten: Structure, Molecular Dynamics, and Activation of π-Acidic Ligands[M(NMes)2Cl2(dme)] (M = Mo 1, W 2; Mes = mesityl) or the trans-phosphane complexes [M(NMes)2(PMe3)2Cl2] (3, 4) are reduced by C8K in the presence of PMe3 to give diamagnetic d2 complexes [Mo(NMes)2(PMe3}3] (5) and [W(NMes)2-(PMe3)3] (6). At least one PMe3 ligand in 5 and 6 is readily substituted by more π-acidic substrates such as ethene, ethyne, 2-butyne, and P(OEt)3. The reaction with ethene leads to [Mo(NMes)2(η2-C2H4)(PMe3)2] (7) and [W(NMes)2-(η2-C2H4)(PMe3)2] (8). Furthermore, pentacoordinate complexes [Mo(NMes)2(η2-C2Me2)(PMe3)2] (9), [W(NMes)2(η2-C2H2)(PMe3)2] (10), and [W(NMes)2(PMe3){P(OEt)3)2] (11) have been synthesized from 5 or 6. The X-ray structure analysis of 8 reveals a trigonal-bipyramidal geometry about tungsten with both arylimido groups perfectly lying in the equatorial mirror plane. The ethene ligand is occupying the third equatorial position. The C2 vector is oriented perpendicular to the WN2 plane. Dynamic NMR studies are consistent with a tbp geometry being also present in solution at the low-temperature limit. At higher temperatures a rapid exchange of the PMe3 ligands with noncoordinated phosphane according to a dissociative mechanism is observed.
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  • 96
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    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1865-1870 
    ISSN: 0009-2940
    Keywords: Sulfane, bis[bis(trimethylsilyl)amino]-, reaction with mixtures of tellurium-containing chalcogen halides ; 1,3,4λD4,2,5-Trichalcogenadiazoles, 4,4-dihalogeno- ; 1,3,4λD3,2,5-Trichalcogenadiazolium salts, 4-halogeno ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preparation and Characterisation of Five-Membered Tellurium-Containing Chalcogen-Nitrogen Ring Systems  -  Structure of [ClTeNSNS+]2[Cl-][AsF-6]The reaction of [(Me3Si)2N]2S with TeX4/SeCl4- or TeX4/SCl2 mixtures leads to the formation of covalent five-membered and , respectively. Treatment of 2a and 2b with Ag+Y- (Y- = BF-4, AsF-6, SbF-6) in liquid SO2 provides the cationic ring systems and 3d-f (X = Br). If the solvent is CH2Cl2 the double salts and 4d-f (X = Br) are obtained. The structure of has been determined by X-ray crystallography. The selenium-containing five-membered ring systems are accessible by reaction of AgAsF6 with 1a and 1c, respectively.
    Additional Material: 2 Ill.
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  • 97
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    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1871-1875 
    ISSN: 0009-2940
    Keywords: Oxidation by HOF ; Hypofluorous acid ; Addition compounds of HOF and HF with acetonitrile ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidation Reactions with HOF and Adducts of HOF and HF with AcetonitrileIn acetonitrile solution HOF oxides CF3SSCF3 via CF3S(O)nSCF3 (n = 1, 2) to yield [CF3S(O)2]2O. Analogously, CF3Se(O)OH and CF3SeX (X = Cl, Br) are oxidized via CF3Se(VI) intermediates to provide finally [CF3Se(O)2]2O. With CH3CN at low temperatures HOF and HF form 1:1 adducts, whose structures have been elucidated by low-temperature X-ray structure analysis. Additional proof for the formation of CH3CN · HF in the liquid phase is provided.
    Additional Material: 3 Ill.
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  • 98
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1887-1889 
    ISSN: 0009-2940
    Keywords: Borazine, molecular packing, difference electron density maps ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The molecular and solid-state structure of borazine has been determined at 115 and 160 K by single-crystal X-ray crystallography. The molecular structure has C2 symmetry with small deviations from the expected D3h symmetry. The mean value of the BN bond length is 1.429(1) A and the interbond angles of the six-membered ring are 117.1(1)° at the boron atoms and 122.9(1)° at the nitrogen atoms (mean values). Similar to benzene an unambiguous assignment of the molecular symmetry is not possible.  -  The crystal packing is not comparable to any known phase of benzene, and surprisingly the molecules are not stacked having coplanar rings. Instead, the molecules are found in tilted layers. No significant intermolecular interaction could be detected. The generated difference electron density maps show the typical distribution pattern for polar bonds.
    Additional Material: 3 Ill.
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  • 99
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    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1891-1894 
    ISSN: 0009-2940
    Keywords: 1,2-Azaboroles, phosphanyl-substituted, X-ray structure analysis ; Thallium-, 1,2-azaborolyl- ; Stereoselectivity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2-Azaborolyl Complexes, XXX[1].  -  Phosphanyl-Substituted 1,2-Azaboroles1-tert-Butyl-2-methyl-1,2-azaborolyllithium (LiAb, 1) and TlCl equilibrate at -75°C in THF under action of light to TlAb (2) and LiCl. Compound 2 decomposes above -50°C with elimination of thallium and the neutral isomers 1-tert-butyl-2,5-dihydro-2-methyl-1H-1,2-azaborole and 1-tert-bu-tyl-2,3-dihydro-2-methyl-1H-1,2-azaborole. Whilst 1 reacts with Ph2PCl in only very small amounts to give the expected Ph2P-substituted azaborole ring 3, TlAb (2) forms this compound by reaction with Ph2PCl in high yields. The yellow oily 3 is characterized by 1H-; 11B-, 13C-, and 31P-NMR data. The Me3Si-substituted derivative 1-tert-butyl-3-(diphenyl-phosphanyl)-2,3-dihydro-2-methyl-3-(trimethylsilyl)-1H-1,2-azaborole (5), available via 4, the Li salt of 3, and ClSiMe3, forms yellow crystals which could be used for an X-ray structure analysis. As expected, the Ph2P and Me3Si groups substitute the boron neighboring C3 atom of the planar ring framework. The crystal structure of 5 shows the two expected enantiomers.
    Additional Material: 1 Ill.
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  • 100
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1895-1900 
    ISSN: 0009-2940
    Keywords: Tin, diorganyl-, bis(maltolate) ; Tin, butyl-, tris(maltolate) ; Tin, tributyl-, maltolate ; Tin, dichloro-, bis(mal-tolate) ; Maltolates, tin ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of organotin(IV) maltol complexes R4  -  xSnLx (1-4, 6; x = 1-3) and the dichloro-compound Cl2SnL2 (5) have been prepared and characterized on the basis of their IR-, 1H-, 13C- and 119Sn-NMR data. While an X-ray crystal structure analysis of Ph2SnL2 (4) and Cl2SnL2 (5) reveals distorted cis-octahedral structures, the Me2SnL2 molecule (2) adopts a skew-trapezoidal bipyramidal configuration with a very significant difference in the Sn-O(keto) bond distances. The tris-maltol complex BuSnL3 (6) exhibits a distorted pentagonal-bipyramidal geometry with the butyl carbon and a hy-droxy oxygen constituting the axial orientations.
    Additional Material: 5 Ill.
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