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  • 1990-1994  (755)
  • 1975-1979
  • 1890-1899
  • 1993  (755)
  • Inorganic Chemistry  (727)
  • crystal structure  (135)
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  • 1990-1994  (755)
  • 1975-1979
  • 1890-1899
Year
  • 1
    ISSN: 1572-8862
    Keywords: Vanadium ; phenylhydrazine ; nitrogenase ; 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 Addition of phenylhydrazine to a mixture of VCl3 · THF/N,N-propyl-bis (salicyladimine) and sodium hydride yielded a trinuclear vanadium complex, V3(μ3-O)(μ-Cl)Cl6(μ-η1-η1PhNHNH2)2(PhNHN H2)2(THF), containing two bridging and two terminal phenylhydrazine ligands. The product has been crystallographically characterized (P21/n, a=12.949(2) Å,b=24.061(4) Å,c=22.504(4) Å, β=107.22(1) deg.,V=6697(2) Å3 withZ=4) and was found to contain the first example of bridging monosubstituted hydrazine (phenylhydrazine) ligands.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular engineering 3 (1993), S. 43-59 
    ISSN: 1572-8951
    Keywords: Heteropolymolybdates ; heteropolytungstates ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The chemistry of polynuclear oxometalate anions is dominated by molybdenum and tungsten in their highest oxidation state. During the past twenty years this class of compounds has attracted much attention because of their variable applications, e.g. as reagents in analytical procedures, as industrial catalysts and as potential anticancer drugs. In order to obtain model systems for the investigation of the catalytic activity of heteropolyanions we have synthesized and structurally characterized some organo derivatives of polyoxoanions. We secondly focus on Sb(III) and Bi(III) heteropolytungstates to examine the important influence of the unshared electron pair on the resulting structures and properties. Some of these compounds may be regarded as supramolecular aggregates showing inclusion phenomena. In 9 two [SbW9O33]9− anions are linked by a set of six sodium ions forming a nearly planar hexagon. The sodium ions are enveloped by an oxygen cage formed by terminal oxygen atoms of the polyanions and by water molecules. Furthermore, the four anions [Sb2W22O74(OH)2]12−, [Sb2W20Fe2O70(H2O)6]8−, [Sb2W20Co2O70(H2O)6]10− and [Bi2W20Fe2O68(OH)2(H2O)6]6− (in10, 11, 12, 13) may be regarded as transition metal complexes of novel [Sb2W20O70]14− or [Bi2W20O70]14− anions which are serving as ligands. The octahedral coordination sphere of each transition metal is formed by three oxygen atoms of the anion and completed by three water molecules. The Sb(III) heteropolyanion, [Na2Sb8W36O132(H2O)4]22− in (14) includes two sodium and four antimony ions besides four water molecules. Each anion consists of four β-B-SbW9-Keggin fragments linked together by four SbO4-groups, incorporating two sodium and four water molecules effecting an additional connection of the subunits.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 271 (1993), S. 50-55 
    ISSN: 1435-1536
    Keywords: Polytetrafluoroethylene ; copolymer ; crystal structure ; chain folding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Molecular-mechanics calculations are performed on model folds proposed in the literature for single crystals of polytetrafluoroethylene crystallized in the phase stable below 19°C, in order to evaluate how they are modified when a fluorine atom is substituted by a bulky group, as occurs in fluorinated copolymers of tetrafluoroethylene. Only intramolecular effects are taken into account (isolated-chain model). An exhaustive analysis has been carried out of tetrafluoroethylene-hexafluoropropylene copolymer. Moreover, the lower energy folds found for such a copolymer have been examined for copolymers with chlorotrifluoroethylene and perfluoroalkylvinylethers, as comonomers. Our calculations show that all the considered comonomers can be arranged in the model folds proposed for the homopolymer, according to the imposed geometric constraints.
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  • 4
    ISSN: 1572-9001
    Keywords: Atomic displacement ; molecular motion ; vibrational analysis ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Atomic displacement parameters determined from a single-crystal X-ray-diffraction study on K2Ru(SO4)2 * 6H2O are analyzed in the molecular mean field approximation. The motion of SO2 2− can be described with a rigid-body model, whereas for [Ru(H2O)6]2+ internal stretching motion and coupling between stretching motion and overall translation are found to be necessary for explaining the observed atomic displacement parameters. Frequencies and force constants of internal motion are not significantly affected by such couplings. K2Ru(SO4)2 * 6H2O crystallizes in the monoclinic space groupP21/c (No. 14), witha = 6.1211(7)Å,b = 12.226(2) Å,c = 8.916(2)Å,β = 105.11(1)°,Z = 2 at 160 K anda = 6.1402(7)Å,b = 12.274(2)Å,c = 8.957(1)Å,β = 105.25(1)°,Z = 2 at 295 K. The structure was refined to a finalR(F) of 0.017 at 160 K and of 0.019 at 295 K for 1438 and 1299 observed reflections withF 0 〉 6σ(F0) and sin θ/λ 〉 0.617 Å1−.
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  • 5
    ISSN: 1572-8862
    Keywords: Platinum ; ruthenium ; crystal structure ; heteronuclear cluster
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract From the reaction of Ru(CO)5 and Pt(COD)2, COD = 1, 5-cyclooctadiene, the new platinum-ruthenium heteronuclear cluster complex Pt2Ru4(CO)18,1, was obtained in 60% yield.1 has a folded ladder-like structure with alternating pairs of ruthenium atoms and platinum atoms. The cluster of1 can be split to yield the known compound PtRu2(CO)8(η2-dppe),2, (54% yield) by reaction with 1, 2-bis(diphenylphosphino)ethane, dppe, at 25°C. When1 was treated with excess dppe at 40°C, thebis-diphos compound3, PtRu2(CO)6(μ-η2-dppe)2 was obtained (39% yield). Under the similar reaction conditions,2 was converted to3 in 44% yield. All these complexes were characterized by single crystal X-ray diffraction analyses. Compounds2 and3 both contain a triangular cluster of one platinum and two ruthenium atoms, but in2 the bidentate ligand, dppe, chelates the platinum atom and in3 the two dppe ligands bridge the two Pt-Ru metal-metal bonds. Crystal data for1: space group C2/c,a=12.542(2)Å,b=15.350(4)Å,c=15.252(3)Å, β=105.32(2)°,Z=4, 2192 reflections,R=0.025. For2: space group P21/c,a=14.351(2)Å,b=13.486(3)Å,c=19.218(3)Å, β=108.48(1)°,Z=4, 3029 reflections,R=0.027. For3: space group P21/c,a=18.836(6)Å,b=15.559(5)Å,c=23.259(7)Å, β=111.26(2)°,Z=4, 4204 reflections,R=0.038.
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  • 6
    ISSN: 1572-8862
    Keywords: Tungsten ; chloride ; hexatungsten ; 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 hexanuclear tungsten cluster complex [W6(μ3-Cl)8Cl6]2−,1 was isolated as a salt of the cation (MeO2CCH2)2N(H)CH2CH2N(CH2CO2Me)2+, EDTEH+, by crystallization from methanol solvent of the product obtained from the reaction of (H3O)2[W6(μ3-Cl)8Cl3] with the disodium salt of ethylenediaminetetraacetic acid. The compound was charcterized by single-crystal X-ray diffraction analysis. The cluster anion contains an octahedral arrangement of six tungsten atoms with chloride ligands bridging the eight triangular faces of the cluster and one chloride ligand terminally coordinated to each of the six tungsten atoms. The cation (EDTEH)+ achieves its positive charge by protonation of one of the nitrogen atoms. Crystal data: space group = P21/a,a=10.689(2) Å,b=22.931(6) Å,c=12.093(3) Å, β=98.41(2)°,Z=2, 2476 reflections,R=0.028.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymers and the environment 1 (1993), S. 65-80 
    ISSN: 1572-8900
    Keywords: Biodegradable plastic ; microbial degradation ; bacterial poly(d-(−)-3-hydroxybutyrate) ; crystal structure ; physiological behavior
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract As one of a series of studies concerning the relationship between the higher-order structure and the biodegradability of a biodegradable plastic, the effects of the crystal structure of the plastic on microbial degradation were investigated. Bacterial poly(d-(−)-3-hydroxybutyrate) (PHB) films which had a wide range of crystallinity were prepared by the melt-quenching method. Results of the microbial degradation indicated that the development of crystallinity evidently depressed the microbial degradability. From scanning electron microscopy (SEM) observations, it is suggested that the microbial degradation proceeded in at least two manners. One was preferential degradation of the amorphous region leaving the crystalline lamellae intact, which was considered to be a homogeneous enzymatic degradation over the surface. The other was nonpreferential spherical degradation on the surface. The SEMs indicate that the spherical holes were the result of colonization by degrading bacteria. The holes varied in size and number with the change of crystal structure. Therefore, it is considered that the crystal structure of PHB also influenced the physiological behavior of the degrading bacteria on the PHB surface.
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  • 8
    ISSN: 1572-9001
    Keywords: Cobaltocene ; molecular geometry ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The molecular and crystal structures of the monoclinic modification of cobaltocene Cp2Co (P21/n, Z=2) was determined at 100 K and 297 K with new sets of X-ray diffraction data (MoKα radiation, 3995 and 6534 reflections, refinement toR = 0.026 and 0.030 using 1061 and 1299 independent observable reflections, respectively). At 297 K the structure is disordered (similar to the isomorphous ferrocene and nickelocene) with two distinct orientations of the ring, differing in occupancy factors (80% and 20%) and by a rotation angle in the ring plane of approximately 34°. Just as for nickelocene but in contrast to ferrocene, no sharp phase transition was found on cooling Cp2Co to 100 K, but an essential ordering of the Cp-ring position was detected with a decrease of the contribution of the second minor orientation to nearly 10%. On the basis of a careful analysis of the molecular geometry, crystal packing, and anisotropic atomic displacement parameters, a dynamic temperature-dependent nature of the disorder in Cp2Co is assumed.
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  • 9
    ISSN: 1572-8862
    Keywords: Molybdenum ; acetate, carboxylate ; hexamolybdenum ; 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 hexamolybdenum cluster complex [Mo6(μ3-Cl)8(O2CMe)6]2−, 1 was isolated as the Bu4N+ salt in 71% yield from the reaction of (Bu4N)2[Mo6(μ3-Cl)8Cl6] with AgO2CMe in CH2Cl2 solvent. The compound was characterized by single crystal X-ray diffraction analysis. The cluster contains an octahedral arrangement of six molybdenum atoms with eight chloride ligands bridging the eight trianglar faces and six carboxylate ligands terminally coordinated through one oxygen atom to each of the six molybdenum atoms. Crystal data: space group =P21/n,a=10.713(3)Å,b=14.43(1)Å,c=21.919(4)Å, β=94.37(2)°,Z=2, 1965 reflections,R=0.036.
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  • 10
    ISSN: 1573-1111
    Keywords: 12-membered crown ethers ; crystal structure ; conformation peculiarities ; X-ray analysis ; CH...O contacts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The crystal structures of two 12-membered crown ethers, benzo-12-crown-4 (1) and naphtho-12-crown-4 (2), have been determined by X-ray analysis. Both structures are molecular. Compound1 is monoclonic,P21/b,a=8.466(3),b=8.019(3),c=33.590(10) Å, γ=90.99(3)o. The unit cell contains two crystallographically independent molecules of1 with similar conformations. Compound2 is also monoclinic,P21/a,a=24.148(8),b=14.535(4),c=7.987(5) Å, γ=102.87(2)o. Two independent molecules in the unit cell have significantly different conformations.
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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 15 (1993), S. 159-165 
    ISSN: 1573-1111
    Keywords: Dibenzo-30-crown-10 ; crystal structure ; complexation ; dysprosium isothiocyanate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Crystalline [Dy(NCS)3(dibenzo-30-crown-10)(H2O)2]·H2O·MeCN can be obtained by slowly evaporating a reaction mixture of Dy(NCS)3·nH2O with dibenzo-30-crown-10 in a solution of acetonitrile. The material crystallizes in the monoclinic space groupP21/n, the cell parameters area=11.450(5),b=23.284(4),c=18.424(6)Å, β=106.28(4)°,V=4715Å3,M=968.47,D x=1.36 g cm−1, μ=17.80 cm−1,F(000)=1972,Z=4.2740 independently observed [I≥3σI] reflections were used in the final least-squares refinement leading to an agreement index ofR=0.085. The Dy(III) ion coordination geometry approximates a square antiprism, involving two water oxygens and three dibenzo-30-crown-10 oxygen atoms and three isthiocyanate nitrogens. Hydrogen bonds are formed between the two water molecules and four uncoordinated crown ether oxygen atoms.
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 15 (1993), S. 341-349 
    ISSN: 1573-1111
    Keywords: Molecular asymmetry ; calixarene ; acetone ; clathrate ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The crystal and molecular structure of the 1:1 clathrate of the asymmetric calix[4]arene,1, and acetone has been determined by X-ray analysis. The crystal data are: tetragonal, space groupP4/n,a=b=12.574(6),c=12.572(6) Å,V=1988(2) Å3,Z=2,D x =1.111 g cm−3,D m =1.108 g cm−3. Least-squares refinement based on 1131 observed reflections withF 0〉3σ(F 0) and anisotropic temperature factors led toR=0.096. In spite of the molecular asymmetric calixarene1 the crystal structure has high symmetry, because a part of the host and guest molecules are in disordered states.
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 15 (1993), S. 385-398 
    ISSN: 1573-1111
    Keywords: Hydrogen bonding ; alicyclic diol ; helical tubulate ; crystal structure ; ferrocene ; squalene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The inclusion compounds of 2,8-dimethyltricyclo[5.3.1.13,9]dodecane-syn-2,syn-8-diol,3, with ferrocene and with squalene have been prepared. The crystal structures of these helical tubulate compounds: (3)3·(ferrocene)0.75 [P3121,a=b=13.7480(6),c=7.0312(5) Å,Z=1,R=0.038] and (3)3·(squalene)0.23 [P3121,a=b=13.677(1),c=7.0533(9) Å,Z=1,R=0.042] are described.
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  • 14
    ISSN: 1573-1111
    Keywords: Werner clathrate ; nickel octahedral complex ; tetrahydrofuran ; crystal structure ; NMR ; molecular recognition ; hydrocarbon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract This paper addresses the general question: what are the significant guest properties selected by this host when interacting with guest molecules in the liquid phase, resulting in cocrystallization of the host and guest? In particular, to what extent do π electrons in a guest molecule effect its potential as a guest? Werner clathrates of the host [Ni(NCS)2(4-ViPy)4] with mixtures of tetrahydrofuran (THF) and cyclic hydrocarbons as guests have been synthesised and their structures elucidated. Clathrate (1): [Ni(NCS)2(4-ViPy)4](1.78 THF)(0.22 cyclohexane), crystallizes in the orthorhombic space groupP bcn a=9.976(6),b=20.630(25),c=19.861 (4) Å,V=4087Å3,Z=4,R=0.087 for 1461 reflections; (2): [Ni(NCS)2(4-ViPy)4](1.76 THF)(0.24 cyclohexene),P bcn ,a=9.987(7),b=20.614(4),c=19.898(4)Å,V=4096Å3,Z=4,R=0.084 for 1304 reflections; (3): [Ni(NCS)2(4-ViPy)4](0.48 THF)(0.52 1,3-cyclohexadiene), tetragonalI41/a,a=16.898(3),b=16.898(3),c=26.463(6)Å,V=7556Å3,Z=8,R=0.120 for 1698 reflections; (4): [Ni(NCS)2(4-ViPy)4](0.36 THF)(1.04 1,4-cyclohexadiene),I41/a,a=16.986(4),b=16.986(4),c=25.896(15)Å,V=7472Å3,Z=8,R=0.103 for 2025 reflections; (5): [Ni(NCS)2(4-ViPy)4](0.35 THF)(1.05 benzene),I41/a,a=17.102(10),b=17.102(10),c=25.498(8)Å,V=7458Å3,Z=8,R=0.118 for 2200 reflections; (6): [Ni(NCS)2(4-ViPy)4](3 benzene), triclinicP1,a=10.432(24),b=11.155(9),c=21.581(7)Å, α=78.70(5), β=82.60(7), γ=74.09(13)°,V=2361Å3,Z=2,R=0.078 for 3427 reflections. Host-guest ratios and, for mixtures of guests, guest1/guest2 ratios, were elucidated by density and NMR. We show that the conformational freedom of the substituted pyridines is not the primary reason for the clathrating ability of Werner hosts. All six structures show no host-guest interaction at the level of van der Waals interactions. As non-bonding interactions are not observed between the host and guest, this study shows that the above host's selectivity by enclathration of particular guest molecules cannot be accounted for by solid state structural analysis.
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  • 15
    ISSN: 1573-1111
    Keywords: Iminophosphoranes ; amine inclusion compounds ; 13C CPMAS NMR spectroscopy ; salt-like crystalline aggregates ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The crystal and molecular structure is reported for the inclusion compound 2-[o-(triphenylphosphoranylidenamino)benzyliden]amino-1H-2,3-dihydroindazol-3-one/isopropylamine/water3b. The crystal structure consists of discrete dimeric salt-like aggregates joined together by strong N+−H...−O−C hydrogen bonds between pairs of centrosymmetrically-related indazolonate anions and isopropylammonium cations. Six other inclusion compounds have been prepared and characterized by NMR [with propylamine (3a), withtert-butylamine (3c), withsec-butylamine (3d), withtert-pentylamine (3e), with 1-methylbutylamine (3f) and withiso-pentylamine (3g)]. Two different arrangements are found, both with the host being in the anionic form. The guests are either: (i) one protonated amine and one water molecule (3b and3f); or (ii) one protonated amine and the corresponding neutral amine (3a, 3c, 3d, 3e and3g).
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 16 (1993), S. 267-272 
    ISSN: 1573-1111
    Keywords: Crown ether ; ytterbium nitrate ; phen ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The title complex was prepared by reacting Yb(NO3)3 (12-crown-4) with 1,10-phenanthroline (hereafter phen) in acetone. It crystallized in the triclinic space group $$P\bar 1$$ witha=10.095(5),b=17.415(4),c=8.710(2) Å α=92.45(2), β=115.83(3), γ=74.08(3)0 andD c=1.85 g cm−3;Z=2. The metal ion in this complex is nine-coordinated to three bidentate nitrate ions, two nitrogen atoms of a phen and a water molecule. The crown ligand is hydrogen bonded to the coordination water molecule. The symmetry change of the crown ether is also discussed.
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  • 17
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Proteins: Structure, Function, and Genetics 16 (1993), S. 205-213 
    ISSN: 0887-3585
    Keywords: calcium binding ; crystal structure ; protein stability ; site-directed mutagenesis ; subtilisin ; X-ray crystallography ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A version of subtilisin BPN′ lacking the high affinity calcium site (site A) has been produced through genetic engineering methods, and its crystal structure refined at 1.8 Å resolution. This protein and the corresponding version containing the calcium A site are describedand compared. The deletion of residues 75-83 was made in the context of four site-specific replacements previously shown to stabilize subtilisin. The helix that in wild type is interrupted by the calcium binding loop, is continuous in the deletion mutant, with normal geometry. A few residues adjacent to the loop, principally those that were involved in calcium coordination, are repositioned and/or destabilized by the deletion. Because refolding is greatly facilitated by the absence of the Caloop, this proteinoffers a new vehicle for analysis and dissection of the folding reaction. This is among the largest internal changes to a protein to be described at atomic resolution. © Wiley-Liss, Inc.
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  • 18
    ISSN: 0887-3585
    Keywords: thrombin ; bifunctional inhibitor ; crystal structure ; hirutonis ; drugdesing ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The crystal structure of the complexes of hirutonin-2 and hirutonin-6 with human α-thrombin have been solved and refined to R-factors of 0.169 (2.0 Å resolution) and 0.162 (201Å), respectively. Hirutonins belong to a family of bifunctional inhibitors bearing a noncleavable moiety mimicking the scissile bond. Hirutonin-2 is an analog of (D)Phe-Pro-Arg-Gly-hirudin49-65; hirutonin-6 has the same N-terminal tripeptide connected to a shortened fibrinogen exosite-binding part by a short, non-peptidyl linker. The hirutonin-6 molecule is well defined in the electron density with the exception of the C-terminal Leu-h61. The linker follows near the bottom of the canyon connecting the active site with the exosite, forms a short antiparallel β-sheet-like arrangement with Leu-40-Leu41 and makes van der Waals contacts with Glu39-Leu40-Leu41 of thrombin. In the thrombin-hirutonin-2 complex, the N- and C-terminal parts of the inhibitor are well or dered (except the C-terminal Gln-h65) while the central portion of the linker is partially disordered. The glycine analog in the P1′ position of hirutonin-2 assumes a conformation similar to that of the canonical form (Bode and Huber (1992) Eur. J. Biochem. 204 : 433-451) and supports the identification of the S1′ site as restricted by His57, Trp60D, Lys60F, and the Cys42-Cys58 disulfide bridge. The carbonyl oxygen of the P1 arginine residue is located in the oxyanion hole formed by the NH groups of Gly193 and Ser195, while the carbonyl carbon is positioned within a short distance, 2.8 Å, from the Oγ of Ser195. This resembles the conformation of the substrate-like inhibitors bound to other serine proteases. The N-terminal (D)Phe-pro-Arg fragment common to both inhibitors binds to thrombin in a fashion very similar to that of other inhibitors having this motif. The binding of the C-terminus of hirutonins to the fibrinogen-binding exosite is similar to that observed in hirudin and hirulog complexes. © 1993 Wiley-Liss, Inc.
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  • 19
    ISSN: 1573-9171
    Keywords: titanasilanes ; titanasilazanes ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An X-ray structural study of two titanium-containing organosilicon compounds, (Me3Si)3SiTi(NEt2)3 (1) and ClTi[N(SiMe3)2]3 (2), has been performed. The conformation of molecule1 in a crystal is staggered (approximate inherentC 3 symmetry), the Ti-Si and Ti-N bond lengths are 2.671(2) and 1.874–1.890(5) Å, respectively. A crystal of1 consists of one type of enantiomers (the space group is P41212; the absolute configuration has been determined). The structure of2 studied previously has been refined to the value of R=0.029 on the basis of 3442 reflections (the absolute structure has been determined), the Ti-Cl and Ti-N bond lengths are 2.260(1) and 1.926(1) Å, respectively. The strong distortions in the symmetry of the valence environment of the N atoms in the molecules of1, 2, and related structures are caused by electronic effects, in which the conformation of the relevant molecular fragments plays a determining role.
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  • 20
    ISSN: 1573-9171
    Keywords: synthesis ; crystal structure ; azepinethiones ; trimethylsilyl derivative
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The title compounds were prepared and X-ray analysis was performed (R = 0.064 and 0.035 for 1309 and 1637 reflections, respectively). In the former the intramolecular S→Si coordination interactions are absent and the Si atom has undistorted tetrahedral coordination with an S...Si distance of 4.034 Å. Crystals of the latter are built of centrosymmetric dimeric H-complexes (S...H(N) 2.58 Å, the S...HN angle 168°).
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  • 21
    ISSN: 1573-9171
    Keywords: peroxosolvates ; potassium fluoride ; monoperoxosolvate ; thermal stability ; crystal structure ; hydrogen bond
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Potassium fluoride peroxosolvate KF-H2O2 was obtained upon action of a 30% aqueous solution of hydrogen peroxide on solid potassium fluoride dihydrate. As compared to other peroxosolvates, KF-H2O2 is characterized by the highest thermal stability: the decomposition rate constantk 1, at 120°C is 1.4 10−3 min−1, the enthalpy of H2O2 addition to KF is 8.1 kcal/ mol. The correlation between the high stability of KF-H2O2 and the absence of catalytic properties of KF towards H2O2, and the formation of strong intermolecular O-H...F and intramolecular O-H...O hydrogen bonds in the crystal is discussed.
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  • 22
    ISSN: 1573-9171
    Keywords: synthesis ; crystal structure ; pentacoordinated silicon ; chelate cycle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The X-ray diffraction structural study of the (N-Si)-chelate of 2-(chlorodimethyl-silylmethylthio)-1-pyrroline was carried out (R = 0.033 for 1894 reflections). The Si atom has a somewhat distorted trigonal bipyramidal coordination with the Cl and N atoms in axial positions. The Si-Cl and Si-N distances (2.423(1) and 1.945(1) Å) belong, respectively, to the longest and shortest known Si-Cl and Si-N distances in pentacoordinated silicon derivatives with an axial N-Si-Cl moiety.
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  • 23
    ISSN: 1573-9171
    Keywords: iron(II) and ruthenium(II) complexes ; synthesis ; carbonyl, cyclopentadienyl, benzoate ligands ; crystal structure ; X-ray diffraction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Complexes of Fe(II) and Ru(II) of the general formula Cp(OC)2MOC(O)C6H4X-p, where M=Fe, X=H, F (1, 2) or M=Ru, X=H, F (3, 4) have been prepared by reactingp-XC6H4COOAg with [CpFe(CO)2]2 or CpRu(CO)2I. The crystal structures of complexes1–3 have been determined using X-ray diffraction. Compounds1 and3 are isomorphous. The COO group in1–3 is coordinated as a monodentate ligand. As the latter and the CO ligands are electronically non-equivalent, the coordination of the Cp ligand to the metal is slightly asymmetric.
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  • 24
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    Electronic Resource
    Springer
    Russian chemical bulletin 42 (1993), S. 1149-1151 
    ISSN: 1573-9171
    Keywords: Pt(dddt)2 ; organic conductors ; 5,6-dihydro-1,4-dithiin-2,3-dithiolate((dddt)2−) ; sulfur-containing platinum complexes ; crystal structure ; synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A neutral metal complex, [Pt(dddt)2]° (1), has been obtained by oxidation of the [Pt(dddt)2]− anion with excess (Bu4N)AuBr4 in nitrobenzene. Crystallographic data for 1∶a=17.854(9) Å,b=18.409(9) Å,c=4.717(5) Å, γ=68.83(2)°, space group P21/n,Z=4,d calc=2.55 g/cm3. In1 two independent centrosymmetric [Pt(dddt)2]° molecules are packed in stacks that form layers parallel to the (110) plane. The molecules of1 in the layers have shortened S...S contacts 3.491(9) Å, and 3.594(10) Å. The average bond lengths Pt-S 2.242(7) Å, S-C 1.71(2) Å and C=C 1.40(3) Å, together with the square-planar coordination of Pt in PtS4, suggest considerable conjugation in the metal cycles.
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  • 25
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    Springer
    Russian chemical bulletin 42 (1993), S. 1415-1417 
    ISSN: 1573-9171
    Keywords: vanadatrane ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An X-ray diffraction study of a substituted vanadatrane-1-one (space groupPna21,R= 0.019 for 1394 reflections, the absolute structure was determined) showed that the geometry of its atrane framework is similar to that of the Si- and Ge-analogs. The bond lengths are: V=O, 1.614(2) Å; V←N, 2.329(2) Å; V-O, 1.800–1.806(2) Å. The deviation of the V atom having distorted trigonal bipyramidal coordination from the equatorial plane of the O atoms is 0.35 Å, the 0=V←N bond angle is 179.4(1)°.
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  • 26
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1923-1940 
    ISSN: 0887-6266
    Keywords: poly(4,4′-oxybibenzoate) ; polymerization ; morphology ; transitions ; crystal structure ; disclination domains ; Iamellae ; single crystals ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 4-Acetoxy 4′-carboxy biphenyl has been polymerized from solution, the bulk melt, and in constrained thin films, all below the melting point of the monomer as measured by differential scanning calorimetry (DSC). An isothermal sublimation-recrystallization-melting (and chemical change)-polymerization-crystallization process is proposed. From solution and in the thin films, single crystals consisting of ca. 100 Å thick lamellae are observed, with evidence for monomer addition-reaction on the end (top and bottom) surfaces. The bulk samples are fibrous, the “fibers” consisting of whisker-like single crystals. The polymer is highly heat and radiation (electron beam) resistant, with numerous successive electron diffraction (ED) patterns from the same crystal or sheared sample permitting comparison of the changes in ED patterns with transitions seen by DSC at ca. 350, 530, and 590°C. Phase I (a = 7.8, b = 5.5, c = 10.8 Å), a possible phase II (a = 15.6, b = 3.6 Å c = unknown), and a phase III (a = 9.0, b = 5.2 = √3a, c = 10.8 Å). Phases I and II are seen in samples polymerized at temperatures at and below 310°C; phase III is observed in samples polymerized at and above 350°C and in sheared samples. © 1993 John Wiley & Sons, Inc.
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  • 27
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1713-1723 
    ISSN: 0887-6266
    Keywords: phthalocyanine siloxane ; crystal structure ; epitaxial growth ; high-resolution electron microscopy ; molecular imaging ; polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thin films of SiPc(OH)2 (Pc = phthalocyanine) were formed epitaxially on the (001) surface of mica by vacuum deposition and were then polymerized by heat treatment. The molecular packing of the SiPc(OH)2 was determined by electron diffraction and high-resolution electron microscopy as triclinic\documentclass{article}\pagestyle{empty}\begin{document}${\rm P\bar 1} $\end{document} having dimensions a = 0.727, b = 1.307, c = 0.688 nm, α = 102.5, β = 104.2, and γ = 97.4°. This monomer crystal grows with its c-axis parallel to the a-axis of the substrate mica and its bc-plane parallel to the (001) surface of mica. By heat treatment at 320°C, the SiPc(OH)2 polymerized with the c-axis of the polymer parallel to the c-axis of the monomer. At 420°C, the c-axis of the polymer became parallel to the a*-axis of the monomer (i.e., perpendicular to the film surface). From high-resolution electron microscopy of partially polymerized specimens, the polymerization was shown to start at the edges of small monomer crystals. This may be considered to be due to the volume expansion during the polymerization. © 1993 John Wiley & Sons, Inc.
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  • 28
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    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1759-1767 
    ISSN: 0887-6266
    Keywords: rigid rod polymer ; thermotropic ; aromatic polyester ; fiber ; modulus ; crystal structure ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Fiber spinning and mechanical properties of four rigid polyesters with alkoxy substituents of different length and placement were evaluated. Properties of oriented fibers from the polymer with dodecyloxy substituents on the terephthalate moiety, PTA12HQ, were significantly affected by the crystal modification. At room temperature the following properties (tensile modulus E, tensile strength σb, and strain at break εb) could be obtained: E = 9.5 GPa, σb = 85 MPa and εb = 1.1% for phase Lf (the “frozen in layered mesophase”); E = 10.4 GPa, σb = 59 MPa and εb = 0.6% for modification A; E = 17.3 GPa, σb = 158 MPa and εb = 1.2% for modification B. Because of the higher amount of main chains per cross sectional area the polymer with hexyloxy side chains, PTA6HQ, showed better properties at a comparable degree of molecular orientation: E = 24 GPa, σb = 270 MPa, εb = 1.4%. Fibers obtained from the polyester with dodecyloxy substituents on the hydroquinone moiety, PTAHQ12, were too brittle to handle. The polyester with dodecyloxy substituents on both moieties, PTA12HQ12, was spun from the isotropic melt. Because of the obtained low degree of orientation, properties (E = 1 GPa, σb = 40 MPa, and εb = 6.3%) were governed by interactions between the chains (the main chains are not load-bearing). © 1993 John Wiley & Sons, Inc.
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  • 29
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 30
    ISSN: 0009-2940
    Keywords: Diphosphamanganacyclopropanes ; Alkyne insertion ; Alkyne addition ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal-;Containing Heterocycles: Preparation, Properties, Reactions, LXXX.  -  Insertion and Addition Reactions on Diphosphamanganacyclopropanes with Activated AlkynesThe thermally and kinetically stable diphosphamanganabicyclooctadienones 3a  -  e [R2 = tBu: R1 = iPr (a), nPr (b), Ph (c); R2 = Cy: R1 = nPr (d), Ph (e)] are obtained by the reaction of the alkyne (CCO2Me)2 with the diphosphamanganacyclopropanes (OC)4Mn-PR12=PR2 (2a  -  e). Depending on steric factors the formation of 3a  -  e occurs in two different ways. In a first step the alkyne is inserted into the P  -  P bond of 2a  -  e to give the kinetically labile five-membered rings 1a  -  e. Subsequently another alkyne is added to the PR2 and a CO group of 1a  -  e to give 3a  -  e. In an alternative way the alkyne is added first to the PR2 and a CO group of 2a with formation of the diphosphamanganabicyclohexenone 4a. Insertion of a second alkyne into the P  -  P bond of 4a affords the bicyclooctadienone 3a. Compound 2a, 3c, and 4a have been characterized by X-ray structural analyses.
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  • 31
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 11-15 
    ISSN: 0009-2940
    Keywords: Indium compounds ; Indate, tetrafluorenyl ; Indate, chlorotrifluorenyl ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fluorenylindates: Compounds with Weak In  -  C BondsIn diethyl ether, fluorenyllithium reacts with indium(III) chloride to yield a lithium tetrafluorenylindate (1). Recrystallisation from THF gives [Li(THF)4][In(C13H9)4] (2). If the reaction is carried out in THF, the chlorotrifluorenylindate [Li(THF)4]-[ClIn(C13H9)3] (3) is isolated. According to crystal structure analyses 2 has long and weak In  -  C bonds [224.8(5) - 230.3(5) pm], while these distances in 3 are somewhat shorter [222.9 (5) - 226.7(4) pm].
    Additional Material: 3 Ill.
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  • 32
    ISSN: 0009-2940
    Keywords: Dinuclear complexes ; Iron complexes ; Platinum complexes ; Silyl complexes ; Phosphide bridges ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Transition Metal Silyl Complexes, 44.  -  Preparation of the Binuclear Silyl Complexes (CO)3(R3Si)Fe(μ-PR′R′′)Pt(PPh3)2 by Oxidative Addition of (CO)3(R′R′′HP)Fe(H)SiR3 to (C2H4)Pt(PPh3)2The complexes (CO)3(R′R′′HP)Fe(H)SiR3 (1) [PHR′R′′ = PHPh2, PH2Ph, PH2Cy; SiR3 = SiPh3, SiPh2Me, SiPhMe2, Si(OMe)3] react with Pt(C2H4)(PPh3)2 to give the dinuclear, silyl-substituted complexes (CO)3(R3Si)Fe(μ-PR′R′′)Pt(PPh3)2 (2) in high yields. Upon reaction of 2 (R = R′ R′′ = Ph) with CO, the PPh3 ligand at Pt being trans to the PPh2 bridge is exchanged, and (CO)3(Ph3Si)Fe(μ-PPh2)Pt(PPh3)CO (3) is formed. Complex 3 is characterized by an X-ray structure analysis. The rather short Fe  -  Si distance [233.9(2) pm] and the infrared spectrum of 3 indicate that the Fe  -  Pt bond is quite polar.
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  • 33
    ISSN: 0009-2940
    Keywords: Osmium tetraoxide ; Oxidation ; Fluoroolefins ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Multiple Bonds Between Main Group Elements and Transition Metals, CIX.  -  Structural Aspects of Fluoroolefin Oxidation by Osmium Tetraoxide: Halogenated Osmate Esters and Their ProductsThe crystal and molecular structures of the first fluorinated osmate ester 1, the dioxoosmium(VI) dichloride 2, and the dioxoosmium(VI) oxalate 3 have been determined by single-crystal X-ray diffraction. They all contain the trans-osmyl group {OsO2}2+ and cis-oriented sets of ligands, typical of complexes (py)2OsO2X2 (py = pyridine). Increasing electron-withdrawing power of the ligands X entails shortening of the OsN bonds, resulting in higher stability of these complexes against dissociation of pyridine.
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  • 34
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2255-2257 
    ISSN: 0009-2940
    Keywords: Gallane, chlorobis(supermesityl) ; Rearrangement ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis, Structure, and Rearrangement of Chlorobis(2,4,6-tri-tert-butylphenyl)gallaneThe title compound 1 is easily obtained from GaCl3 and 2 equvialents of supermesityllithium. According to an X-ray structure analysis one of the supermesityl rings shows a large deviation from planarity. Heating of 1 in vacuo gives mainly two products: an isomer of 1 in which one of the supermesityl groups is bound to Ga by one of its tert-butyl groups (2) and a benzo[b]gallolane (3) formed by elimination of HCl, X-ray structure analyses and full NMR (1H, 13C) data are provided for 1 and 2, MS and characteristic NMR (1H, 13C) data for 3.
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  • 35
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2265-2268 
    ISSN: 0009-2940
    Keywords: Chemoselectivity ; Protonolysis ; Transfer hydrogenation ; Alkenes, reduction of ; Alkynes, reduction of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The H2PO2 - NH4+ · H2O/Pd-C system acts as an unusually powerful reducing agent, which is able to reduce cyclooctene to cyclooctane, Δ9,10-octalin to decalins, α- and β-pinenes to pinanes at room temperature in high yield without the formation of byproducts. This system selectively reduces each of these compounds or partly (alkynes to alkenes), depending on the competition between the transfer hydrogenation to give alkanes and the protonolysis to give hydrogen gas on the palladium catalyst.
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  • 36
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2269-2273 
    ISSN: 0009-2940
    Keywords: Bipyrroles ; Tetrapyrroles ; Tripyrroles ; Polypyrroles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electrochemical and chemical oxidative α,α'-coupling of 3-methoxy-4-methyl-2-pyrrolecarboxylic acid (2) and its ethyl ester 4 is compared with that of the corresponding 4-methoxy-2-pyrrolecarboxylates (1 and 3 respectively). The β-alkoxy substituent exerts a strong directing influence on its vicinal α-position, which in the case of compounds 2 and 4 determines the 2,5'-coupling and allows the isolation of the corresponding 1H,2'H-2,2'-bipyrrole 6 in the case of 4. For 2 the polypyrrole can be obtained by exhaustive electrochemical or chemical coupling, whereas in the case of 1 only the corresponding tetramers are formed. The structures of these tetrapyrroles, already described in the literature, here obtained by oxidation of 4-alkoxy-2-pyrrolecarboxylic acid (1), have been reexamined: they are mixtures of tetramers with zwitterionic structure, have at least two substitution patterns and are partially oxidized to the corresponding bipyrrolylidenes.
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  • 37
    ISSN: 0009-2940
    Keywords: Molybdenum(VI) compound ; Siloxanes ; Vanadium(V) compound ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Model Reactions to Anchor Molybdenum and Vanadium Oxides on Silica-Oxygen SurfacesThe eight-and twelve-membered ring compounds [(tBu)21-Si(O)2MoO2]2 (1) and [(tBu)2Si(O)2V(O)Cl]3 (2) have been prepared by the reaction of di-tert1-butylsilanediol or its dilithium salt with MoO2Br2 or VOCl3, respectively. Single crystal X-ray structure analyses of 1 · 2 py and 2 have been performed. Crystals of 1 · 2 py contain two molecules of 1 · 2 py and four additional molecules of pyridine in the unit cell.
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  • 38
    ISSN: 0009-2940
    Keywords: Diastereoselective synthesis ; Homoallylic alcohols ; 1,3-Diols, homoallylic ; β1-Hydroxyalkyl ketones ; 2,5-Dihydro-1H1-boroles ; 1,2-Oxaborolanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1-Phenyl-3-borolenes CH2CR1=CR1CH2BPh) (1a: R1=H; b: R1=Me) react with aldehydes R2CHO to give cis-1,2-oxaborolanes CH2CR1[CR1(=CH2)]CR2R3OBPh (2, R2 = e.g. Me, Ph, CH=CH2, tBu, CCl3, R3 = H). Yields are nearly quantitative. Stereoselectivities usually are 100% (but only 95% for R2=CH=CH2, 97% for R2=Me). Oxidation with NaOH/H2O2 in THF affords homoallylic anti-1,3-diols HOCR2R31-CR1[CR1(=CH2)]CH2OH (3). An X-ray diffraction analysis of 3a (R2=p1-tolyl) proves the assigned stereochemistries. Ketones R2R3CO react analogously. Ketenes R2CCO form 5-alkylidene-4-vinyl-1,2-oxaborolanes (4), which tend to undergo double-bond migration. Oxidation produces two types of β1-hydroxylalkyl ketones R22CHCOC[(E)=CHMe]CH2OH (5) and R22CHCOCMe[CMe=CH2]CH2OH (6).
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  • 39
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 305-317 
    ISSN: 0009-2940
    Keywords: cis-1,2-Diborylalkenes, electron acceptors, anion sponge ; Diborates, hexaorgano, μ1-hydro, μ1-alkoxy, alkali metal salts ; Borates, hydrotriorgano- ; Substituent exchange, diborates ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organosubstituted cis-1,2-Diborylalkenes as Electrophilic ChelatesTriethylborane (1), 9-ethyl-9-borabicyclo[3.3.1]nonane (9-ethyl-9-BBN) (2), and the cis-1,2-diborylalkenes (Z)1-R2BC(R′)=C(Et)BEt2 [3: R=Et, R′=Me; 4: R,R′=Et; 5: R=Et, R′=Ph; 6: R2=C8H14, R′=Et; 7: R=Ph, R′=Et] react with alkali metal salts MX [M=Na, K; X=H, OMe, OtBu, OSiMe3, OSiEt3] in toluene to give the borates MX-1, MX-2, and the cyclic cis-1,2-diborates M, resp., [e.g. KH-3 to KH-7; NaOMe-4 to NaOMe-6; KOtBu-4, KOSiMe3-4, KOSiEt3-4] with BHB-and B(OR)B-bridges (IR, Multi NMR). Reaction of 1, 2, and 3-6 with KCN leads to the monoborates KCN-1, KCN-2, and to the acyclic cis-1,2-diborates KCN-3 to KCN-7.  -  The cis-2-Boryl-1-silylalkenes (E)1-Me3SiC(R′)=C(Et)BEt2 [8: R′=Me; 9: R′=Et] and KX [X=H, CN, OMe] form the acyclic borates K[Me3SiC(R′)=C(Et)1-BEt2X]. The cyclic salts KOtBu-4 and KOSiEt3-4 undergo a B1-substituent exchange to the acyclic cis-1,2-diborates K[Et3BC(Et)=C(Et)B(Et)OR] (K-10: R=tBu; K-11: R=OSiEt3).
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  • 40
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 73-77 
    ISSN: 0009-2940
    Keywords: 1-Alkynyl disulfides ; Thioketenes, thio-substituted ; α-Dithiones ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of novel 1-alkynyl disulfides 1 is described together with their 1-thiapropargyl  -  3-thiaallenyl rearrangement and a [1,3]-sigmatropic shift of 1-alkynyl amino disulfides, followed by rearrangement of the aminothio-substituted thioketenes so formed.
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  • 41
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 285-288 
    ISSN: 0009-2940
    Keywords: Nitriles ; Hydroboration ; Bis(9H-9-borabicyclo[3.3.1]nonane) ; N-Base-Organoboron adducts ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hydroboration of benzo-, tolu-, p1-methoxybenzo-, or pivalonitriles with bis(9-borabicyclo[3.3.1]nonane) (9H-9-BBN)2 affords the corresponding 9-aldimino-9-borabicyclo[3.3.1]1-nonanes (1a  -  d) in about 80% yields. Compounds 1a and 1d readily react with an excess of (9H-9-BBN)2 to form the 1:1 adducts 2a or 2d, respectively, containing a NB2H four-membered ring (X-ray structure of 2a). The adducts 2 are thermally rather stable. Compound 2a is converted to benzylbis(1,5-cyclooctanediylboryl)amine (3a) only after 48 h at reflux in mesitylene. Compounds 1a  -  d are stable towards strong N-bases. Compound 1d reacts with Et2O · BF3 to form 9-fluoro-9-borabicyclo[3.3.1]nonane (4) and the 1:1 cyclic adduct (5d) of (2,2-dimethylpropylideneamino)difluoroborane (6d) and 1d.
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  • 42
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 331-337 
    ISSN: 0009-2940
    Keywords: Neodymium complexes ; Cyclopentadienyl, substituted and functionalized ; Volatility ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complexes of the Lanthanides, IV[1].  -  Alkyl-and Donor-substituted Cyclopentadienyl Complexes of NeodymiumNeodymium trichloride reacts with the potassium salt K(DoCH2CH2Cp) (2c, Do=OMe; 2d, Do=NMe2) of the functionalized cyclopentadienyls in THF to yield the sublimable homoleptic complexes Nd(DoCH2CH2Cp)3 (3c, d). Under the same conditions, K(iBuCp) (2a) yields the adduct Nd(i1-BuCp)3(THF) (3a′), which is obtained free of THF by thermal treatment. The silylamide route is applied to synthesize the homoleptic neopentylcyclopentadienyl derivative Nd-(NeopCp)3 (3b). The alkyl-substituted complexes, particularly the isobutyl derivative, show a remarkable volatility. The first solvent-free, monomeric complex of the type „LnCp2Cl“, namely Nd(Me2NCH2CH2Cp)2Cl (4), is obtained from NdCl3 and two equivalents of 2d.
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  • 43
    ISSN: 0009-2940
    Keywords: Crotonate, lithium ; Fumarate, dilithium ; Maleate, dilithium ; Polymerization solid-state ; Conductivity, ionic ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crystal Structure, Solid-State Polymerization, and Ionic Conductivity of Alkali Salts of Unsaturated Carboxylic Acids, 3[1].  -  Investigations on Lithium Crotonate, Dilithium Fumarate-Tetrahydrate, and Dilithium Maleate MonohydrateThe structures of lithium crotonate (1), dilithium fumarate tetrahydrate (2), and dilithium maleate monohydrate (3) have been determined by single-crystal X-ray diffraction and are discussed in detail in view of the possibility to realize a topochemical polymerization. Compounds 1 and 3 can be polymerized thermally, however this results in a complete breakdown of the crystal structure. Impedance measurements show a weak ionic conductivity in the case of 2. The other compounds and the products of thermal polymerization are isolators with a mean Dkr′ of about 4.0.
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  • 44
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 399-404 
    ISSN: 0009-2940
    Keywords: Chromium complexes ; Aniline as an η61-ligand ; Voltammetry, cyclic ; Nerst-Clark plots ; Acid dissociation constants ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal π Complexes of Benzene Derivatives, XLI[1].  -  Bis(η61-aniline)chromium: Synthesis, Redox Properties and Brønsted BasicityBis(η61-aniline)chromium (6) has been prepared by protodesilylation of its N,N,N′,N′1-tetrakis(trimethylsilyl) derivative 5, which is accessible by metal-atom ligand-vapor cocondensation (cc). Bis(η61-dimethylaniline)chromium (3) is obtained directly from cc. The couples 3+/0 and 6+/0 feature the most negative redox potentials E1/2 ever reported for bis(arene)1-metal complexes. According to EPR spectroscopy, applied to the radical cations 3+· and 6+· the site of oxidation is largely localized on the metal. The pH dependence of E1/2 is cast in Nerst-Clark plots, whose breaks supply the pKs values of the mono-and diprotonated forms of 3 and 6. η61-Coordination to CrI increases the basicity of aniline by three pK units, whereas η61-coordination to Cr1 effects a decrease by more than seven pK units. The first and second dissociation constants of the organometallic bis(ammonium) ions 3(H+)2 and 6(H+)2 differ by 2.7 pK units. This interval reflects the interaction of the two basic centers in 3 and 6 which approaches that of p1-phenylenediamine. Thus, conjugation across the bis(η61-arene)chromium unit is virtually uninhibited.
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  • 45
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2353-2355 
    ISSN: 0009-2940
    Keywords: Ylides ; Distonic ions ; Neutralization-reionization mass spectrometry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The recently described (Maier et al.[2]) title compound is not only viable in an argon matrix (10 K) but is also accessible in the gas phase. Electron impact ionization of (CH3)3CCX2NC (X = H, D) gives rise to HCNCX2+, which can be successfully neutralized in a beam experiment.
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  • 46
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2357-2360 
    ISSN: 0009-2940
    Keywords: α-Oxo ketenes ; Wolff rearrangement ; Matrix isolation ; Ketenes, α-oxo- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title compound 8a was generated by both flash vacuum pyrolysis and matrix photolysis of diazoquinolone 7 and identified by Ar-matrix IR spectroscopy and mass spectrometry. Trapping of the highly reactive α-oxo ketene 8a with methanol leads to β-keto ester 9, whereas dimerization of 8a furnishes spiro compound 10.
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  • 47
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2363-2365 
    ISSN: 0009-2940
    Keywords: Dimethoxysulfane ; Dimethoxydisulfane ; Photoelectron spectra ; Calculations, MO ; Ligand properties ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The He(I) photoelectron spectra of dimethoxysulfane (1) and dimethoxydisulfane (2) have been recorded. The lowest energy ionizations in the PE spectrum of 1 can be explained by assuming C2 symmetry. They can be described as arising from linear combinations between the 3p lone-pair at sulfur and 2p lone-pairs at the oxygen atoms. A comparison between the calculated MO sequence of 2 for different conformations and the first PE bands shows a good agreement with an OSSO torsional angle near 90°. The highest occupied MOs of 2 can be described as linear combinations between the 3p MOs of the S2 unit and linear combinations between the 2p AOs of the oxygen atoms.
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  • 48
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2367-2371 
    ISSN: 0009-2940
    Keywords: Tin, (alkylthio)stilbene complexes of ; cis-stilbene-α-thiol, β-(methylthio)-, tin(IV) complexes of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The S-methyl-cis-stilbene-α,β-dithiolate of Sn(IV), Sn[Ph(S)C=C(SCH3)Ph]4, has an octacoordinate structure with two sets of four covalent and coordinate Sn-S and Sn-S(CH3) bonds of 2.425(3) and 3.599(3) Å, respectively. Both types of Sn-S bonds are close to being tetrahedral, the coordination geometry is a distorted cube. This unprecedented structure appears to involve conventional covalent and outer-sphere coordinative Sn-S bonds. In the diphenyl derivative Ph2Sn[Ph(S)C=C(SCH3)Ph]2 the SnC2S2 core formed by the covalent Sn-C and Sn-S(thiolato) bonds is tetrahedral, but two coordinate outer-sphere Sn-S(CH3) bonds of 3.500(3) Å are also present. In the related SnCl2[Ph(S)C=C(SCH3)Ph]2 the presence of the polar Sn-Cl bonds prevents outer-sphere bonding; the coordination geometry is distorted octahedral. In the triphenyltin derivative Ph3Sn[Ph(S)C=C(SCH3)Ph] the coordination geometry is tetrahedral, the thiol-thioether ligand being monodentate with the SCH3 group in a non-interactive position.
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  • 49
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2379-2382 
    ISSN: 0009-2940
    Keywords: Steric overcrowding ; Trisphosphane, linear, bismethylene-bridged ; Molybdenum, complexes with bis- and trisphosphanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis[(di-tert-butylphosphanyl)methyl]methylphosphane[1]The synthesis of [(di-tert-butylphosphanyl)methyl]dimethyl-phosphane (3) and of the title compound 5 is described. 5 reacts with sulfur to form the trisulfide 6. Both 3 and 5 behave as bidentate ligands in forming the molybdenum complexes 8 and 10, which are characterized by single crystal X-ray structure determinations. 10 reacts with sulfur to yield the sulfide 11, which decomposes in solution within 6 h.
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  • 50
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2373-2378 
    ISSN: 0009-2940
    Keywords: Imidazolium manganese complexes ; Carbene complexes ; Cyclization ; Carbyne manganese complexes, cationic ; Cyanamides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Coupling of Cyanamides with a Carbyne Ligand - Formation of η2-(C,N)-Imidazolium Complexes and Ansa-Carbene ComplexesHerrn Prof. Dr. Ernst Otto Fischer zum 75. Geburtstag gewidmet.Dicarbonyl(cyclopentadienyl)(phenylcarbyne)manganese complexes [Cp(CO)2Mn≡CPh]+X- (1-X) (X = BF4, BCl4) react with dimethyl- (2a), diethyl- (2b), and diisopropylcyanamide (2c) in five-fold excess by a head-to-tail cyclization of two cyanamides with the carbyne ligand to give η2-(C,N)-imidazolium complexes (3a-c-X). As byproducts ansa-amino(alkylide-neamino)carbene complexes (4a-c) are formed in which a N=C(Ph) group bridges the carbene carbon and the Cp ring. With increasing excess of the cyanamide the product ratio 3-X: 4 increases. Among the products of the reaction of 1-X with the cyanamides N≡CNR2 [NR2 = N(iBu)2, N(Bzl)2, N(Me)Ph] no imidazolium complexes 3-X are detected, only ansa-carbene complexes 4 are isolated. PMe3/H2O or pyridine/H2O displaces the heterocyclic ligand from 3a-BF4. The structure of 3a-BF4 is established by an X-ray analysis.
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  • 51
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2389-2391 
    ISSN: 0009-2940
    Keywords: Butatriene, phosphanyl-substituted ; Phosphane ligands ; Phosphane sulfide ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Treatment of bis(diphenylphosphanyl)ethyne with potassium diphenylphosphide in tetrahydrofuran leads to the formation of tetraphenyldiphosphane Ph2P-PPh2 and the title compound (Ph2P)2C=C=C=C(PPh2)2 (1). A mechanism is proposed for this process. Compound 1 reacts with elemental sulfur to give the tetrasulfide [Ph2(S)P]2C=C=C=C[P(S)Ph2]2 (2). The crystal structures of 1 and 2 have been determined by single-crystal X-ray diffraction. In both cases the linear butatriene unit shows strongly alternating C=C bond lengths as predicted in theoretical studies.
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  • 52
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2383-2388 
    ISSN: 0009-2940
    Keywords: Silazane, phenoxy- ; Metal amides (Li, Cu, Ag, Cd) ; Metal-metal interactions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Structurally Different Metal Amides (Li, Cu, Ag, Cd) with the Chelating Ligand [tBu-N-SiMe2-O-C6H4-O-SiMe2-N-tBu]2-Herrn Professor Heinrich Nöth zum 65. Geburtstag gewidmet.The amino hydrogen atoms in the silylamine o-C6H4O2(Me2SiN(H)tBu)2 (1) can be replaced by monovalent (Li, Cu, Ag) or divalent (Cd) metallic elements. Whereas the lithium compound is obtained as an ether adduct, [C6H4O2(Me2SiNtBu)2]Li2 · OEt2 (2), the copper and silver compounds are solvens-free. The latter two form similar dimers comprising four metal atoms: [C6H4O2(Me2SiNtBu)2]2Cu4 (3) and [C6H4O2 (Me2SiNtBu)2]2Ag4 (4). The cadmium compound is also a dimer with two ligands and two cadmium atoms making up the molecule, [C6H4O2(Me2SiNtBu)2]2Cd2 (5). X-ray structure analyses reveal that in all compounds the metallic elements are highly coordinated by N and O interactions, with coordination numbers of 4 (2, 3, 4) and 5 (5). The oxygen contacts are quite long ranging from 260 to 301 pm. In the Cu und Ag compounds quadratic planar arrangements at the metals are found (bridged by nitrogen) with distances Cu-Cu 262.6(2)-270.1(2) and Ag-Ag 291.7(1)-301.8(2) pm.
    Additional Material: 4 Ill.
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  • 53
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 575-580 
    ISSN: 0009-2940
    Keywords: Silaethene derivatives ; Furans ; Cycloaddition reactions ; Rearrangements ; Sila heterocycles ; Diels-Alder reactions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sila Heterocycles, XXII[1]. - Diels-Alder Reactions of Dichloro(neopentyl)silaethene with Furans and Rearrangement of the Resulting Bicycles into Monocyclic Si - O Seven-Membered Ring compoundsThe reaction of trichloro(vinyl)silane (1) and LitBu (2) initially leads to the α1-lithio adduct Cl3SiCH(Li)CH2tBu (3) which can be trapped by trimethylsilyl triflate yielding the C1-silylated product [Cl3SiCH(SiMe3)CH2tBu (5)]. 1,2-LiCl elimination from 3 gives dichloro(neopentyl)silaethene [Cl2Si=CHCH2tBu (4)] as intermediate. This can be established by insertion of 4 into the Si - O bond of Me3SiOMe to Cl2Si(OMe)CH(SiMe3)CH2tBu (6). 4 is a dienophile of high activity and reacts with the furans 7 - 9 to give the [4 + 2] cycloaddition compounds 10 - 12. These Diels-Alder products are thermally unstable and decompose slowly at room temperature into the starting furans and tetrachlorodisilacyclobutane (15). Under thermolysis conditions (3 d/17°C) they rearrange into the monocyclic Si - O seven-membered ring compounds 16 - 18. A mechanism for the 7-Oxa-2-silabicyclo[2.2.1]hex-5-en → 1-Oxa-2-silacyclohepta-4,6-diene rearrangement is proposed.
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  • 54
    ISSN: 0009-2940
    Keywords: Heterodinuclear cyclooctatetraene complexes ; Paramagnetism ; ESR of electron spin doublet and of electron spin quartet ; Redox properties ; d-d Interactions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cooperative Effects in π1-Ligand-Bridged Dinuclear Complexes, XIII[1]. - Unexpected Weak d-d Interactions in Synfacial Heterodinuclear μ1-Cyclooctatetraene Complexes of the Type {(CpCr)[(CO)3M′]}μ1-Cot (M′=Fe, Cr, W)The heterodinuclear complexes {(CpCr)[(CO)3M′]}μ1-Cot (Cot=C8H8; M′=Fe, Cr, W) (5 - 7) and {(Cp*Cr)[(CO)3Cr]}μ1-Cot (Cp*=C5Me5) (9) are synthesized by the reaction of the corresponding mononuclear Cot complexes CpCr(η61-Cot) (4) and Cp*Cr(η61-Cot) (8), respectively, with M′(CO)3(EtCN)3 (M′=Cr, W) and with Fe2(CO)9. The CrFe compound 5 is obtained in very low yield only. However, much better yields of 5 are achieved in the reaction of CrCl2 and CrCp2 with (CO)3Fe(η41-Cot) (10) in the presence of an excess of Zn. X-ray structure determinations of 5 and 6 reveal synfacial configurations of the CpCr and M′(CO)3 units with a μ1-η5:3- and μ1-η4:51-Cot bonding mode for 5 and 6, respectively. The metal - metal distances are 2.9369(13) Å for 5 and 2.81(2) Å for 6 indicating metal - metal single bonds. 5 contains 33 valence electrons (ve) and is paramagnetic with one unpaired electron. A well-resolved fluid-solution ESR spectrum of 5 shows a 53Cr and 1H hyperfine structure (hfs). The 1H hfs can be calculated with three different 1H hyperfine coupling constants (1H hfcc) indicative of protons in α1-position with respect to the paramagnetic metal center: one 1H hfcc of the five Cp protons (1.68 G), one of three (3.32 G) and one of two protons of the Cot ligand (5.04 G). This agrees with the Cot bonding mode of the CpCr unit in the crystalline phase. The ratio of 3:2 protons for the Cot ligand prove the rigidity of the Cot ligand on the ESR time scale. The excellent agreement of the ESR data of the liquid and frozen solution ESR spectra of 5 with the ESR data of the mononuclear complex CpCr(η61-Cot) leads to the conclusion that the unpaired electron in 5 must predominantly be chromium-centered. 6, 7, and 9 have 31 ve and are paramagnetic with three unpaired electrons as shown by means of ESR spectroscopy and magnetic measurements. The calculations of the quartet ESR spectra of 6, 7, and 9 reveal zero-field splitting parameters D ranging from 3.6 to 4.8 cm-1 which are similar to that of the mononuclear quartet compound vanadocene. The small range in the parameters D prove the minor influence of the second metal on going from Cr to W. Hence, the three unpaired electrons are assumed to be mainly localized on the Cr center of the CpCr unit. Cyclic voltammetry studies result in the redoxcascade - 2 ⇄ - 1 ⇄ 0 ⇄ + 1 for 5 and 7 at +20°C and for 6 at -35°C. However, at +20°C 6 and 9 only show one electrochemically reversible reduction wave 0/-1, whereas the oxidation 0/+1 and the second reduction -1/-2 are irreversible. The redox potentials indicate a considerable influence of the metal combinations. On the strength of the ESR spectroscopic results and according to the results of crystal structure determinations, an isolobal relationship is drawn between the (CO)3M′(η8 - ×1-Cot) fragment and a cyclic organic π1-ligand with the hapticity × + 1.
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2415-2419 
    ISSN: 0009-2940
    Keywords: Periodic acid, protonation of ; Hexahydroxoiodine(VII) cation ; Hexahydroxoiodine(VII) hydrogensulfate, bimorphism of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Existence of the Hexahydroxoiodine(VII) Cation - Crystal Growth and Structure Analysis of α- and β-H6IO6HSO4*Periodic acid H5IO6 dissolves at 50°C in 90-97% H2SO4 to give the hexahydroxoiodine(VII) cation H6IO6+. Depending on the concentration of the sulfuric acid, two modifications of H6IO6HSO4 can selectively and reproducibly be precipitated. The crystal structures determinations prove the existence of H6IO6+ in the solid state. The crystal structures and Raman spectra of α-H6IO6HSO4 (1a) and β-H6IO6HSO4 (1b) are discussed and compared. The temperature-dependent behaviour of 1a and 1b is studied by means of DTA, temperature-dependent X-ray powder diffraction, and Raman spectroscopy.
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  • 56
    ISSN: 0009-2940
    Keywords: Palladium complexes ; Rhodium complexes ; α-Amino acids ; 2-Iminocarboxylate as ligand ; Chiral glycine ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Biologically Important Ligands, LXVII[1]. - Synthesis of α-Amino Acids from Palladium(II)- and Rhodium(III)-Coordinated Imines and Oximes of α-OxocarboxylatesThe bis-chelate complexes Pd[O2CC(R1)=NOR2]2 (1) and Pd[O2CC(R1)=NR2]2 (2, R2 optically active substituent) are synthesized by template condensation of an α-oxocarboxylic acid with a hydroxylamine or amine component, respectively. Similarly, the Rh(III) complexes Cp*Rh(Cl)[O2CC(R)=N(CHMePh)] (3a: R = H, 3b: R = Me) were obtained from α-oxocarboxylic acids and optically active 1-phenylethylamine. Catalytic hydrogenation of 1 and 2 gives directly the free α-amino acids with, in case of 2, ee's between 0 and 36%. Nucleophilic attack by the carbanions of RC(O)CH2CO2Et and H2NCH(CO2Et)2 at the imino carbon atom of 3a leads to the α-amino carboxylato complexes 4 and 5. - Compounds 4a and 5 have been characterized by X-ray diffraction. Reaction of 3a with NaBH4 or NaBD4 followed by decomposition of the complex with HCl yields N-substituted glycine and N-substituted α-deuterio-glycine, respectively. The diastereoselectivity (70:30) of the α-deuteration could be determined by NMR spectroscopy.
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  • 57
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2429-2432 
    ISSN: 0009-2940
    Keywords: Aspartic acid ; Asparagine ; Diamino carboxylic acid ; Cobalt complexes ; Alkali complexes ; Pentamethylcyclopentadienyl ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Biologically Important Ligands, LXVIII[1]. - Organometallic Asparaginato Cobalt Complexes as Ligands for Alkaline IonsThe trischelate complexes of the dianion of aspartic acid and β-methylaspartic acid (η5-C5Me5)] (R = H, Me) form adducts with alkali iodides MI (M = Li, Na, K). The polymeric structure of (η5-C5Me5)Co(L-asp.-2H+)KI (1c) was determined by X-ray diffraction. In the crystal of 1c the potassium ions are surrounded by five oxygen atoms of the carboxylate groups whereby two oxygen atoms form bridges between two K+ ions. Similarly, trischelate complexes 4 and 5 have been obtained from (η5-C5Me5)Co(CO)I2 and 2,3-diaminopropionic, 2,4-diaminobutyric acid, and asparagine, respectively.
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  • 58
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2437-2439 
    ISSN: 0009-2940
    Keywords: Sulfur tetrafluoride imides ; Fluorosulfonylamines ; Pentafluorosulfanylamines ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of (Fluorosulfonylimino)-λ6-sulfur Tetrafluoride FSO2N=SF4Herrn Professor Pedro J. Aymonino zum 60. Geburtstag gewidmet.FSO2N=SF4 (1) reacts with CsF, HF and CIF to form Cs+N(SO2F)SF5- (2), HN(SO2F)SF5 (3) and ClN(SO2F)(SF5) (5); 5 adds to ethylene to give ClCH2CH2N(SO2F)SF5 (6).
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  • 59
    ISSN: 0009-2940
    Keywords: Cobalt, (η2-thiophosphinito) and (η3-cyclobutenyl) complexes ; Alkyne insertion ; [2 + 2] Cycloaddition ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal-Containing Heterocycles: Preparation, Properties and Reactions, LXXXV[1]. - Consecutive Insertion and [2 + 2] Cycloaddition Reaction of Hexafluoro-2-butyne with an (η2-Thiophosphinito)cobalt complexInsertion of hexafluoro-2-butyne (2) into the Co - P bond of the (η2-thiosphosphinito)cobalt complex (OC)2Ph3PCo(η2-SPt2) (1) and subsequent [2 + 2] cycloaddition to a second alkyne 2 results in the formation of the stable (η3-cyclobutenyl)cobalt complex 3. According to an X-ray structural analysis 3 crystallizes in the triclinic space group P1 with Z = 2.
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2441-2441 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 703-710 
    ISSN: 0009-2940
    Keywords: Pyrazolylborate ligand ; Zinc hydroxide complex ; Enzyme model ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An L3ZnOH Complex as a Functional Model of the Enzyme Carbonic AnhydraseThe tridentate ligand hydrotris(3-tert1-butyl-5-methylpyrazolyl)borate (L3) reacts with zinc perchlorate hexahydrate to form L3ZnOH (1) which is the first mononuclear neutral zinc hydroxide complex. 1 is a structural model of the enzyme carbonic anhydrase due to its tetrahedral coordination with three N-heterocycles and one OH ion as ligands. Its functional analogy to the enzyme involves (a) reversible uptake of CO2 forming the unstable bicarbonate complex L3ZnOCOOH (4) in solution from which the dinuclear carbonate complex L3ZnOC(O)OZnL3 (3) crystallizes, (b) reaction with dialkyl pyrocarbonates forming the complexes L3ZnOC(O)OR (5) which are stable esters of the bicarbonate complex and which are easily hydrolyzed to ROH, CO2, and L3ZnOH, (c) thermal decarboxylation of the ethyl carbonate complex 5b resulting in the ethanolate complex L3ZnOEt (6) which is extremely sensitive to hydrolysis, (d) “inhibition” by small anions due to conversion of 1 into the complexes L3ZnX (7; X=Cl, CN, N3, OAc). The identity of the various L3Zn derivatives is established by NMR methods and structure determinations.
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  • 62
    ISSN: 0009-2940
    Keywords: cis1-Stannyl-boryl-alkenes ; Sulfur bis(trimethylsilylamide) ; N1-Sulfinyl(trimethylsilyl)amine ; NMR, multinuclear ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New heterocyclic systems (1-amino-1λ41-thia-2-azonia-3-borata-1,4-cyclopentadienes 4a and 4b, a 1λ41-thia-2-aza-3-bora-1-cyclopentanone 7 and a 1-trimethylstannyloxy-1λ41-thia-2-azonia-3-borata-1,4-cyclopentadiene 8) are formed by reaction of (E)1-2-diethylboryl-1-trimethylstannyl-1-butene (1a) and (E)1-3-diethylboryl-2-trimethylstannyl-2-pentene (1b) with sulfur bis(trimethylsilylimide) (2) and N1-sulfinyl(trimethylsilyl)amine (3). There is a marked influence of other substituents at the C=C bond on the product distribution. It appears that all reactions proceed via an intermediate borane adduct A. In A the proximity of the electrophilic site of 2 or 3 to various reactive sites of the alkene derivative opens the way to the final products. The proposed structures are supported by consistent 1H-, 11B-, 13C-, 29Si-and 119Sn-NMR data. In the case of compound 4a an X-ray analysis has been carried out.
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  • 63
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 64
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 845-847 
    ISSN: 0009-2940
    Keywords: Hetero[4]radialene ; 1,2-Diphosphetane ; Butadiene, 2,3-bis(chlorophosphanyl)- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2-Diphosphetane 4, the first “1,2-diphospha[4]radialene”, has been prepared in 83% yield by the reductive coupling reaction of 2,3-bis(chloroisopropylphosphanyl)butadiene 3a with lithium in THF. The X-ray crystal structure of 4 was determined, and it shows that 4 is a highly strained 1,2-diphosphetane.
    Additional Material: 1 Ill.
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  • 65
    ISSN: 0009-2940
    Keywords: Spirosilicates, zwitterionic ; Silicon, pentacoordinate ; Bond cleavage, Si - C ; Solid-state NMR, 29Si and 15N ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New Zwitterionic λ51-Spirosilicates: Syntheses, Single-Crystal X-Ray Structure Analyses, and Solid-State NMR StudiesThe zwitterionic spirocyclic λ51-silicates bis[3,4,5,6-tetrabromo-1,2-benzenediolato(2-)][2-(pyrrolidinio)ethyl]silicate (5; and its monohydrate 5 · H2O) and bis[1,2-benzenediolato(2-)]1-[(dimethylammonio)methyl]silicate (6) were synthesized by various methods including Si - C bond cleavage reactions. The crystal structures of 5, 5·H2O, and 6 were investigated by X-ray diffarction. Furthermore, 5, 5·H2O, 6, and the related zwitterionic λ51-spirosilicates 1·1/4 CH3CN, 2·CH3CN, 3·CH3CN, and 4 were characterized by solid-state NMR spectroscopy (29Si and 15N CP/MAS). The pentacoordinate silicon atoms of 5, 5·H2O (two cystallographically independent zwitterions and two crystallographically independent water molecules), and 6 (two crystallographically independent zwitterions) are surrounded by four oxygen atoms and one carbon atom. The coordination polyhedrons around the silicon atoms of 5 and 6 can be described as distorted (5) or nearly ideal (6) trigonal bipyramids, the carbon atoms being in equatorial positions. 5 forms intramolecular and 6 intermolecular (→ for-mation of dimeric units) N - H…O hydrogen bonds. The co-ordination polyhedrons around the two crystallographically independent silicon atoms of 5·H2O can be described as a nearly ideal and slightly distorted square pyramid, respectively, the carbon atoms being in the apical positions. In the crystal lattice of 5·H2O, intermolecular N - H…O O - H…O hydrogen bonds between the zwitterions and water molecules are observed. The results obtained by X-ray diffraction and solid-state NMR spectroscopy are consistent for each compound studied.
    Additional Material: 7 Ill.
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  • 66
    ISSN: 0009-2940
    Keywords: 1,3,2,4-Diphosphadiboretanes, 2,4-bis(dialkylamino)- ; Boranes, (dialkylamino)bis(alkylphosphanyl)- ; Chromium, pentacarbonyl[2,3-bis(dialkylamino)1-1,3,2,4-diphosphadiboretane] complexes ; Chromium, pentacarbonyl[(2,2,6,6-tetramethylpiperidino)phosphane-P]- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Contributions to the Chemistry of Boron, 216[1]. - On the Complex Formation of 1,3,2,4-Diphosphadiboretanes with Pentacarbonylchromium and the Preparation and Reactivity of Borylidenephosphane Complexes2,4-Bis(dialkylamino)1-1,3,2,4-diphosphadiboretanes (R2NBP-CMe3)2 with sterically undemanding amino substituents are prepared together with the corresponding bis(phosphanyl)1-boranes R2NB(PHCMe3)2 by the reaction of R2NBCl2 with Li-P(H)CMe3. Complexes of 1,3,2,4-diphosphadiboretanes with one or two pentacarbonylchromium fragments were obtained by the reaction of the ligands with Cr(CO)5·THF or Cr(CO)5·NMe3. If substituents are sterically demanding, cycloreversion is observed with formation of [(aminoborylidene)1-phosphanyl-P]pentacarbonylchromium compounds tmpB=PR[Cr(CO)5] (10, 29) with an allene-like structure. Complex 29 may also be prepared by HCl elimination from tmp-B(Cl)-P(H)CMe3[Cr(CO)5] (34) with lithium diisopropylamide. This reaction can by reversed be the addition of HCl. The diphosphadiboretane 11 reacts with HCl, ethanol, and secondary amines with cleavage of all BP bonds. The X-ray structures of complexes (Et2NB - PCMe3)2[Cr(CO)5]2 (23) and (iPr2NB - PCEt3)2 [Cr(CO)5] (25) as well as of the diphosphadi-boretanes (Me2NB - PCMe3)2 (11) and (iPr2NB - PCEt3)2 (24) are presented. The intra ring angles of 23 remain almost unchanged upon complexation. In contrast, the B2P2 ring of 25 is slightly folded and its noncoordinated P atom approaches a planar environment.
    Additional Material: 5 Ill.
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  • 67
    ISSN: 0009-2940
    Keywords: Cyclopentadienyl complexes ; Cyclooctatetraenyl complexes ; Yttrium compounds ; Terbium compounds ; Lutetium compounds ; Lanthanoides, organo-, alkoxides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organometallic Compounds of the Lanthanoids, 73[1]. - Synthesis and Structure of New Monocyclooctatetraenyl Complexes of Yttrium, Terbium, and Lutetium[(C8H8)Ln(μ1-Cl)(THF)]2 (Ln=Y, Lu) react with NaOR (R=Ph, C6H3Me2-2,6) to give the dinuclear cyclooctatetraenyl rare earth alkoxides [(C8H8)Ln(μ1-OR)(THF)]2 [R=Ph, Ln=Y (1a), Lu (1b); R=C6H3Me2-2,6, Ln=Y (2a), Lu (2b)]. The reactions of [(C8H8)Ln(μ1-Cl)(THF)]2 with LiOC(tBu)3, NaOSiPh3, and NaC5H3tBu2 result in the formation of (C8H8)LnOC(tBu)3(THF) [Ln=Y (3a), Lu (3b)], (C8H8)LnOSiPh3(THF) [Ln=Y (4a), Lu (4b)], and (C8H8)Tb(C5H3tBu2) (5), respectively. Treatment of (C8H8)Y(C5Me5) with acetylacetone yields (C5Me5)Y(acac)2 (6). The 1H-and 13C-NMR and mass spectra of the new compounds as well as the X-ray crystal structures of 1a and 5 are discussed.
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  • 68
    ISSN: 0009-2940
    Keywords: Organometallic fluorides ; Titanium ; π1-Complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preparation and Reactions of (η51-Pentamethylcyclopentadienyl)1- and (η51-Ethyltetramethylcyclopentadienyl)titanium Trifluoride[1]Compound Cp*TiCl3 (1, Cp*=η51-Me5C5) reacts with an excess of AsF3 to yield the crystalline complex [Cp*TiF3]2·2 AsF3 (2). AsF3 can be removed from 2 in vacuo to give Cp*TiF3 (3). Complex (η51-EtMe4C5)TiCl3 (4) is converted by an excess of AsF3 to (η51-EtMe4C5)TiF3 (5). Compound 3 reacts with a lithium 1,3-diketonate to form the hexacoordinated complex (6) and with a lithium benzamidinate to yield pentacoordinated Cp*TiF2[(Me3SiN)2 C-C6H4OMe-(4)] (7): The reaction of 3 with Ph3PNSiMe3 and C2H2(Ph2PNSiMe3)2 leads to Cp*TiF2NPPh3 (8) and (Cp*TiF2NPPh2)2C2H2 (9), respectively. X-Ray structure analyses of compounds 2 and 5-9 have been performed.
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  • 69
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 941-945 
    ISSN: 0009-2940
    Keywords: Aluminium - aluminium bond ; Dialuminate(5) with three-and fourfold coordinated aluminium ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tetraalkylhydrido-and Tetraalkylmethyldialuminate(5) with Aluminium - Aluminium Bond: [R2Al - AlXR2]- {R=CH(SiMe3)2; X=H, Me}Tetrakis[bis(trimethylsilyl)methyl]dialuminium(4) (1) with an aluminium - aluminium bond reacts with tert1-butyllithium in the presence of the chelating tetramethylethylenediamine (TMEDA) to give a hydridodialuminate(5) 2 [R2Al - AlHR2]- {R=CH(SiMe3)2} by β1-elimination and addition of the hydride anion to one aluminium atom. By treatment of 1 with methyllithium a similar product is formed containing a methyl group bound to aluminium: [R2A1 - AlMeR2]- 3. As shown by crystal structure determination the aluminium - aluminium bond of both molecules is not bridged. Instead, the compounds contain a saturated, four-coordinated aluminium neighbouring an unsaturated, threefold coordinated aluminium atom. While in the hydrogen compound 2 the aluminium - aluminium bond length [266.7(3) pm] remains unaffected in comparison to the neutral starting compound 1, it is lengthened in the methyl derivative 3 by 9 pm to 275.2(3) pm probably due to the higher sterical demand of the methyl group.
    Additional Material: 1 Ill.
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  • 70
    ISSN: 0009-2940
    Keywords: Thiolato ligands ; Nickel complexes ; Hydrogenase models ; Bioinorganic chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mononuclear Nickel Thiolate Complexes Containing Nickel Sites in Different Oxidation States: Molecular Definition of [Ni(SC6H4O)2]2- and [Ni(SC6H4O)2]Herrn Professor Dietrich Mootz zum 60. Geburtstag gewidmet.A solution of NiCl2·6 H2O in EtOH/H2O reacts with nBu3N and o1-mercaptophenol to form [nBu3NH]2[Ni(SC6H4O)2]·EtOH (2) containing the nickel(II) complex [Ni(SC6H4O)2]2- (1). The molecular structures of 1 and its oxidation product, [Ni(SC6H4O)2]- (3), have been determined by X-ray diffraction. With respect to the chemical as well as electrochemical properties of the nickel sites of various hydrogenases, 3 is the first relevant model complex of coordination number four whose structural properties have been determined in different oxidation states.
    Additional Material: 2 Ill.
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  • 71
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1003-1009 
    ISSN: 0009-2940
    Keywords: Diamine ; Host-guest chemistry ; Macrocycle ; Supramolecular chemistry ; Receptor molecule, synthetic ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tailor-Made Host for Piperazine and Related AminesThe 38-membered bis-catechol 4b is obtained by cyclisation of the diacyl dichloride 3c with the diamine 2b in 45% yield, whereas a 68-membered octalactam 7 is formed under similar conditions from 5 and 1b. Bis-catechol 4b is a selective host compound for piperazine (8) and the structurally related diamine 9. Association constants for the 1:1 complexes have been measured by 1H-NMR titration experiments. A nucleobase guest (pterine, 24) was extracted into a hydrochloric acid phase by complex formation with the host 4b. The results are compared with solubility and transport experiments obtained by use of analogous macrobicyclic tris-catechol hosts.
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  • 72
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1015-1021 
    ISSN: 0009-2940
    Keywords: Indigo ; Calculations, AM1 ; cis/trans Isomerization ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: AM1-SCF and AM1-SDCI calculations have been carried out for indigo and three conformers of N,N′1-diacetylindigo in their cis and trans configurations. The molecular structure of trans- N,N′1-diacetylindigo was determined by X-ray diffraction. The calculated ground-state data obtained within the SCF approximation (relative energies, structural parameters) are in excellent agreement with the corresponding experimental values. Potential energy curves (PEC) for the isomerization reaction cis/trans in several electronic states were obtained from AM1-SDCI calculations. For N,N′1-diacetylindigo the ground state PEC has a maximum at a torsion angle about the central C—C bond of 90°, whereas the S1- and T11-state PEC's show minima at the corresponding geometry. For indigo itself significant barriers to the photoisomerization in the S1- and T11-excited states are predicted because of increased NH…OC hydrogen bonding. The results provide an explanation for the phototropic behaviour of N,N′1-diacetylindigo and the photostability of indigo. The calculated enthalpies of activation for the isomerization process cis → trans in the ground state compare well with available experimental data, thus rendering feasible the prediction of the thermal stability of cis isomers not yet synthesized.
    Additional Material: 4 Ill.
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  • 73
    ISSN: 0009-2940
    Keywords: C—C Bond cleavage, kinetics of ; Heat of formation ; Radicals, stability of ; Capto-dative effect ; Geminal substituents, energetic interaction of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Substituent Effects on the Strength of C—C Bonds, 13[1]. - Kinetic and Thermodynamic Stability of α1-alkylated α1-Amino Acid Esters - Energy of Stabilization of α1-Amino-α1-(ethoxycarbonyl)alkyl RadicalsThermolytic cleavage of 1a-c and 2a-c into radicals in solution are clean first-order processes. The activation parameters for C—C bond homolysis were determined. Compared with the corresponding data for hydrocarbons of equal strain a decrease of bond strength of 14.4 kcal/mol results by the combined interaction of the amino and the ethoxycarbonyl substituents. The heat of formation of 5 was determined by combustion calorimetry [δHco (1)=- 1207.75 ± 0.20 kcal/mol] combined with the heat of vaporization (δHvo=13.31 ± 0.10 kcal/mol). Compared with the additive behaviour of group increments the resulting heat of formation (δHfo (g)=- 112.02 ± 0.24 kcal/mol] suggests a synergetic, geminal destabilization of Hsyn=1.9 ± 1.4 kcal/mol. Combination of the kinetic data of bond homolysis of 1a-c and 2a-c with the synergetic ground-state destabilization leads to a synergetic, capto-dative radical stabilization of Hsyn (rad)=6.7 kcal/mol.
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  • 74
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1071-1076 
    ISSN: 0009-2940
    Keywords: Selenium halogen compounds ; Poly(o1-phenylenediselenide), cleavage of ; Oxidative cleavage ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidative Cleavage of Poly(o1-phenylenediselenide)Poly(o1-phenylenediselenide) is cleaved at the Se-Se bond by treatment with SOCl2 to give benzene-1,2-bis(selenenyl chloride) (2) and benzene-1,2-bis(selenium trichloride) (3), respectively. In the solid state 2 is dimerized by Se…Se bonds whereas 3 is monomeric having terminal as well as intramolecular bridging Cl atoms. Treatment of 2 with SbCl5 gives an ionic compound (4) with a dimeric cation exhibiting a weak Se—Se bond and SbCl6- as a counterion 3 reacts with W(CO)6 to give trigonal prismatic dicarbonyl bis(o1-phenylenediselenolato)tungsten (5).
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  • 75
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1091-1100 
    ISSN: 0009-2940
    Keywords: 3,4-Bis(phosphanyl)pyrrolidines ; Palladium complexes ; Rhodium complexes ; Asymmetric hydrogenation ; Phosphanes, chiral ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enantioselective Catalysis, IX[1]. - New Optically Pure 3,4-Bis(phosphanyl)pyrrolidines with Phenyl and Anisyl Groups Including Their Palladium and Rhodium ComplexesMethods for the synthesis of the diastereomeric mixture of the [P(R,S),3R,4R,P′(R,S)]1-1-(tert1-butoxycarbonyl)1-3,4-bis[(2-methoxyphenyl)phenylphosphanyl]pyrrolidines (2a, b, c) are described. For the chromatographic separation and purification of the ligand diastereomers we transformed them into the PdI21-complexes (10a, b, c). The structure of (PR,3R,4R,P′R)1-1-(tert1-butoxycarbonyl)1-3,4-bis[(2-methoxyphenyl)phenylphosphanyl]pyrrolidine-P,P′}diiodopalladium (10 b) was determined by X-ray diffraction. Treatment of the palladium complexes with KCN yielded the pure phosphanes. The rhodium complexes (11a, 11b, 11c), which can be used as catalysts in enantioselective hydrogenations, were obtained by reaction of [Rh(COD)2]BF4 with compound 2a, 2b, or 2c.
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  • 76
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1107-1114 
    ISSN: 0009-2940
    Keywords: Dialkynylsilanes, intermolecular 1,1-ethyloboration of ; 1,1-Vinyloboration, intramolecular ; 3-Borylsiloles, protodeborylation of ; (Ligand)transition metal, η4 complexes of ; Sandwich complex, cyclodiastereomers of ; Siloles, boryl-organo-substituted ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organo-Substituted Siloles by Twofold Organoboration of Di-1-alkynylsilanesMe2Si(C≡CR)2 [R=Me (A), Bu (B), tBu (C), iPent (D), Ph (E), Me3Si (F)], prepared from Me2SiCl2 and MC≡CR (M=Li, Na, K), react with Et3B by 1,1-ethyloboration to form the organo-substituted siloles Me2 (1a - f) in high yields with different reaction rates: F 〉 B ≍ D 〉 A 〉 C 〉 E. Me2Si(C ≡CiPent)(C ≡ CPh) (H) and Et3B give a 5 : 1 mixture of the two regioisomeric substituted siloles 2 and 2′. - 1a and e are deborylated with H2NCH2CH2OH or MeCO2H to 3a and e, respectively. 1a reacts with maleic anhydride to yield the [4 + 2] addition compound 4a. With (OC)5Fe, Cp-Co(C2H4)2, and (CDT)Ni the cycloracemic (ligand)transition metal η41-complexes [(OC)3Fe-1a (5a), (OC)3Fe-3a (6a), CpCo-3a (7a)] and the cyclodiastereomeric η4,η41-complexes Ni-(3a)2 (8a/8a′) are formed. All products were characterized by multinuclear NMR, including measurements of J(29Si13C) and J(13C13C).
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  • 77
    ISSN: 0009-2940
    Keywords: Cycloaddition reactions ; 1,2-Oxaboretanes ; 1,2-Thiaboretanes ; 1,2-Azaboretidines ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Contributions to the Chemistry of Boron, 217[1]. - [2 + 2] Cycloaddition Reactions of 9-Fluorenylidene(tetramethylpiperidino)borane with Carbonyl and Thiocarbonyl CompoundsAmino-9-fluorenylidene-borane 1 reacts with acetone or benzophenone in a [2 + 2] cycloaddition manner to give stable 1,2-oxaboretane derivatives 2. Aldehydes behave similarly but the oxaboretanes formed decompose readily. The esters MeCO2Et and MeC≡C - CO2Me as well as Cp(CO)2Fe - COCH3 also provide access to novel oxaboretane derivatives (2e, f, h). In contrast, no oxaboretane is obtained from 1 and MeC(O)NMe2 and only (tmpBO)n (n=2, 3) was isolated as a decomposition product. The amides MeC(O)NHMe and MeC(O)NH2 also provide no access to cycloaddition since their NH bonds insert into the BC double bond of 1. Thioketones react with 1 to yield 1,2-thiaboretanes 5. Tetramethyl-cyclobutan-1-one-3-thione 8 adds 1 at its carbonyl function regiospecifically to form 9. No reaction between 1 and CO2 was observed, but COS produces an 1,2-oxaboretane-4-thione 7, and CS2 in the form of [CpFe(CO)2]2CS2 the corresponding 1,2-thiaboretane-4-thione 10. Analogously, the ketimine Ph2C=NMe adds to 1 producing the 1,2-azaboretidine 11. X-ray structure determination of the 1,2-oxaboretane 2h reveals a butterfly structure (folding anlge: 159.9°) of the four-membered ring in contrast to the 1,2-thiaboretane 5a whose four-membered ring is almost planar, the folding angle being 176.9°.
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  • 78
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1161-1169 
    ISSN: 0009-2940
    Keywords: Azobenzene units ; Dendrimer ; Divergent synthesis ; Solvent inclusion ; Supramolecular chemistry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dendrimers with bulky repeating units containing up to 43 benzene rings (in 9) have been obtained by using a repetitive divergent synthetic strategy (three generations). The new functional dendrimer 13 containing six azobenzene units at the periphery was synthesized allowing a reversible switching of the shape and size of the molecule upon irradiation. An X-ray structure analysis of the dendritic molecule 3a shows the inclusion of acetonitrile.
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  • 79
    ISSN: 0009-2940
    Keywords: Radical additions ; Acrylonitriles ; Diphenylmethyl radicals ; Steric effects ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Additions of the substituted diphenylmethyl radicals Ar11-Ar2CR 2 (R=CMe3, SiMe3, GeMe3, SnMe3, OSiMe3, CF3, CO2Me, CN) to various acrylonitriles CH2=C(X)CN 3 (X=SMe, SiPr, StBu, OAc, OSiMe3, OSiEt3, OMe, OEt) lead to 1,2-5 or 1,4-adducts 6 (ketenimines), depending mainly on the steric hindrance by the substituents R and X. Bulky substituents like tBu in 2 and tBuS in the acrylonitrile favour the formation of the extended and nearly strainless ketenimine system 6 (1,4-adduct); smaller substituents like OSiMe3 (radical 2) and SMe, OAc, OSiMe3, OSiEt3, OMe, OEt (acrylonitrile) allow isolation of the sterically crowded 1,2-adducts. Substituents of intermediate bulkiness like CF3 (radical 2) and SiPr (acrylonitrile) give a mixture of 1,2-adducts (6cb, hb) and dimers 7 of the adduct radicals 4 (7cb, hb). The voluminous tBu group directly bound to the olefin (3j,k) prevents addition. The latter is generally reversible, and the various adducts 5, 6, or 7 dissociate to the adduct radicals 4 and/or fragment to the initial radicals 2 at temperatures which reflect the steric strains of the corresponding substituents R, X. The complete inertness, even toward the electron-rich olefin 3i, of the electrophilic α1-carbonyl-substituted radicals 2q - s (R=CHO, COMe, COPh) in the above additions is discussed. Additions of the radicals 2a - c, f, i, n, o to the conjugated olefin 3n are described and are in accordance with the conclusion that steric effects predominate in adduct formation, whereas electronic effects are of distinct but minor importance.
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  • 80
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1205-1215 
    ISSN: 0009-2940
    Keywords: Carbanions ; Protonation, diastereoselective ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The diastereoselectivity of the kinetically controlled protonation of carbanions derived from 4-tert1-butyl-1-X-cyclohexanes (1: X=CN, 2: X=CO2Me, 2-Si: X=C(OMe)OSiMe3, 3: X=COPh, 4: X=SO2Ph) is systematically investigated. By variation of (a) the base for deprotonation of 1 - 4, (b) OH-, NH-, and CH-proton sources, (c) added salts, Lewis bases, and acids, (d) solvents (cf. Tables 2 - 5) the cis/trans ratios of diastereomers could be influenced as follows: 1: 41/59→85/15; 2: 26/74→73/27; 3: 26/74→〉93/〈3; 4: 1/99→37/63. The results are discussed with regard to structure and aggregation of 1Li to 4Li and compared with relevant data from the literature. It is concluded that so far an empirical approach to high diastereoselectivities cannot be avoided and that the results cannot be predicted from the ratios obtained by the much slower alkylation reactions.
    Additional Material: 8 Tab.
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  • 81
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1217-1225 
    ISSN: 0009-2940
    Keywords: Bianthronyls ; Bianthronylidenes ; Helianthrone ; Mesonaphthobianthrone ; Photocyclization ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of the novel alkyl-substituted helianthrones 8a, c and mesonaphthobianthrone 9 by photocyclization of the corresponding bianthronylidenes 7a, b is described. Regioselectivity and scope of the photocyclizations of 7a and 7b depend on the substitution pattern. The structures of 7a and 8a have been established by X-ray crystallography and indicate an isomerization about the central double bond of 7a in the photoreaction. The structures of the protonated species of 8a and 9 are elucidated, and their optical absorption and emission behavior is examined.
    Additional Material: 4 Ill.
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  • 82
    ISSN: 0009-2940
    Keywords: Azinium halides, N-(1-haloalkyl)- ; Pyridines, 1,4-dihydro- ; Rates of Formation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-(1-Haloalkyl)azinium halides react with methyl 3-amino-2-butenoate to yield 4-substituted dimethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylates. The rates of formation of the latter compounds are monitored by 1H-NMR spectroscopy. Mechanistic and practical considerations are discussed.
    Additional Material: 1 Tab.
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  • 83
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    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1047-1060 
    ISSN: 0009-2940
    Keywords: Bicyclo[3.3.1]nonane, derivatives of ; 2-Oxatwistane, derivative of ; 2-Oxatricyclo[4.4.0.03,8]decane, derivative of ; Phenyllithium-cerium(III) chloride reagent ; 1,2-Addition to carbonyl groups ; Transannular reaction ; Dipotassium tetraphenylbicyclo[3.3.1]nonadienediide by deprotonation with butylpotassium ; Barbaralane, 2,4,6,8-tetraphenyl-, by oxidation of dipotassium tetraphenylbicyclo[3.3.1]nonadienediide with 1,2-dibromo-ethane ; Thermochromism ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,4,6,8-Tetraphenylbarbaralane - an Orange-Red, Thermochromic Hydrocarbon Devoid of a Chromophore[1,2]The diphenylbicyclo[3.3.1]nonanedione 6 adds phenylcerium-(III) dichloride to afford a high yield of the triphenyl-2-oxa-twistanol 8. In contrast, phenyllithium yields a mixture of tri-phenylhydroxyketone exo-7, tetraphenylbicyclo[3.3.1]nona-nediol 9, and 8. The latter is dehydrated by sulfuric acid in acetic acid to produce the triphenylbicyclo[3.3.1]nonenone 10 in almost quantitative yield. Addition of phenylcerium(III) dichloride to 10 affords a 3:2 mixture of the tetraphenylbicy-clo[3.3.1]nonenols exo- and endo-11 which may be separated by chromatography. Dehydration of the mixture yields quantitatively the tetraphenyldiene 12. On treatment with an excess of butylpotassium in pentane, 12 is converted to the deep violet, crystalline dipotassium salt 17 which may be purified by reprecipitation from its tetrahydrofuran solution with pentane. When the solution of 17 in tetrahydrofuran is slowly added to an excess of 1,2-dibromoethane at -60°C, the dianion is immediately oxidized to produce the tetraphenylbarbara-lane 4 which is isolated in 30% yield as orange-red crystals after chromatography. - The structures of the new compounds are based on spectroscopic evidence and X-ray diffraction analyses of 4, 8, exo-11, and 12. The conformations in solution are inferred on the basis of vicinal proton coupling constants and a comparison with coupling constants calculated with the aid of the Karplus equation from torsional angles obtained by X-ray diffraction analyses. The conformation of exo-11 in solution closely resembles that present in the crystal. - While the barbaralane 4 exists as a pair of very rapidly rearranging degenerate valence tautomers in solution, the degeneracy is lifted in the crystal lattice. As a result, the crystal consists of two rapidly rearranging but non-equivalent valence tautomers in a ratio of 9:1 as estimated from the apparent atomic distance C2-C8 of 4 and the C2-C8 bond length of the model barbaralane 18. - The orange-red colour of 4 in the crystal and in solution results from a pronounced shoulder in the UV/Vis spectrum at 430 nm, the intensity of which strongly depends on the temperature. Thus, 4 is the first barbaralane which exhibits colour though it is lacking a classical long-wavelength chromophore.
    Additional Material: 7 Ill.
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  • 84
    ISSN: 0009-2940
    Keywords: Chromium ; Molybdenum ; Tungsten ; Manganese ; Rhenium ; Iron ; Cobalt ; Diphenylmethane ; Fluorene ; 9,10-Dihydroanthracene ; Cyclohexadiene ; Cyclohexadienyl ; Cycloheptadiene ; Cycloheptatriene ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrocarbon-Bridged Complexes, XXVII[1]. - C—C Coupling of Unsaturated Hydrocarbons of Anionic and Cationic Complexes. Addition of Anions from μ1-(Diphenylmethane)1-, μ1-Fluorene-, and μ1-(9,10-Dihydroanthracene)1-bis(tricarbonylchromium) to Coordinated Olefin, Benzene, Cyclohexadienyl, Cycloheptadienyl, and Cycloheptatrienyl LigandsHerrn Professor Herbert D. Kaesz zum 60. Geburtstag gewidmet.The addition of the anions 1 - 3 of μ1-(diphenylmethane)1-, μ1-fluorene-, and μ1-(9,10-dihydroanthracene)1-bis(tricarbonylchromium) to π1-bonded hydrocarbons (olefin, benzene, cyclohexadienyl, cycloheptadienyl, and cycloheptatrienyl) in cationic complexes of manganese, rhenium, iron, chromium, molybdenum, tungsten, and cobalt provides a synthesis of new hydrocarbon-bridged heterometallic complexes 4 - 10.
    Additional Material: 1 Ill.
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  • 85
    ISSN: 0009-2940
    Keywords: Germanes, silyl ; Stannanes, silyl ; Phosphanes, silyl ; Organometallphosphanes ; Recycling ; Si - Si bond ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions at Silicon-Silicon Bonds, 3[1]. - A New Path to Si - Ge and Si - Sn Bonds: Hexachlorodisilane Cleavage of Organometalphosphanes and (Trichlorosilyl)phosphane RecyclingTrimethyl(trichlorsilyl)germane and -stannane (4, 5) have been prepared through hexachlorodisilane cleavage by germyl-and stannylphosphanes R2PMMe3 (1, 2, R=i1-C3H7, t1-C4H9; M=Ge, Sn). The (trichlorosilyl)phosphane byproduct R2PSiCl3 (3) may be recycled by transmetalation and methylation steps to provide starting germylphosphane (MeGeCl3, 2 MeLi) and stannylphosphane (Me3SnCl, 3 MeLi).
    Additional Material: 1 Tab.
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  • 86
    ISSN: 0009-2940
    Keywords: 3-Azabicyclo[3.3.1]nonanes ; 1-Azaadamantane derivatives ; Clemmensen reduction ; Dichlorination, geminal ; Radical deoxygenation, dehalogenation, nBu3SnH ; Grob fragmentation, regiospecifity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Azabicyclononanes by Fragmentation, II[1]. - Synthesis of 3-Azabicyclononanes by Regiospecific (Grob) FragmentationClemmensen reduction of the non-enolizable β1-dioxo group in the 1-azaadamantanedione derivative 1 gives the β1-hydroxy ketone 2, which is converted to the thioesters 3. Treatment of 3a or 3b with nBu3SnH/toluene yields the partially deoxygenated monoketone 4. Chlorination of 2 with SOCl2 generates 6 (geminal dichlorination). Dehalogenation with nBu3SnH produces 5. On the other hand, 2 can be monochlorinated to give 7, selectively. Preparative Grob fragmentation of the aza-tricyclic skeleton in 7 regiospecifically provides the 3-azabicyclo[3.3.1]nonane derivative 8. An even better access to 8 from 2 proceeds via an intermediate tosylate.
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  • 87
    ISSN: 0009-2940
    Keywords: Palladium complexes, alkyl-and acyl- ; Ether phosphanes ; Fluxional behavior ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A Simple Method for the Preparation of Alkylpalladium Compounds by Pd—O Bond Cleavage in Cationic Bis(etherphosphane)palladium(II) Complexes with Grignard ReagentsHerrn Professor Heinrich Nöth zum 65. Geburtstag gewidmet.The bis(chelate) complexes [Pd(P∩O)2][ClO4]2 (3a - e) react with methylmagnesium chloride with a concomitant cleavage of two weak Pd—O bonds to give the methyl complexes trans1-ClPd(P∼O)2(CH3) (4a - e) (P ∼ O; η1-P1-coordinated; P∩O: η21-O, P1-chelated; Scheme 1). Diffusion of pentane into the reaction mixture of 4a-e in the presence of the formed magnesium salts yields the cationic complexes trans-[Ch3Pd(P∼O)1-(P∩O)][ClO4] (6a, c). The reaction of 3a-e with benzylmagnesium chloride affords the cationic benzyl complexes cis-[PhCh2Pd(P∼O)(P∩O)][ClO4] (8a-e) in which only one Pd—O bond has been cleaved. In the presence of carbon monoxide 4a-e adn 6a, c are transformed into the corresponding acyl complexes CH3C(O)Pd(P∼O)2Cl (5a-e and [CH3C(O)Pd-(P∼O)(P∩O)][ClO4] (7a, c). Whereas at 183 K variable-temperature 31P{1H}1-NMR measurements of 6a, c, 7a, c indicate a non-rigid behavior of the two differently bound ether-phosphanes, the dynamic process is frozen out for 8a-e. By a lineshape analysis of the spectra the thermodynamic parameters ΔG≢, ΔH≢, and ΔS≢ are obtained. According to a crystal structure analysis 3d and 6c crystallize in the monoclinic space group P21/c with Z=4.
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  • 88
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1397-1402 
    ISSN: 0009-2940
    Keywords: 2-Boraindanes ; 2-Benzoboroles, 1,3-dihydro- ; 2-Benzoborole-1,3-diides, 1,3-dihydro- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Boraindanes and 2-(Dialkylamino)1-2-benzoborole Dianionsortho1-Xylene reacts with the Lochmann-Schlosser base to produce a mixture of the potassium derivatives K2[1,2-C6H4(CH2)2] (2) and K[2-MeC6H4CH2] (3). Condensation of 1 + 2 with BCl2(NR2) (R=Me, Et, iPr) affords 2-(dialkylamino)1-2-boraindanes (1a-c) (50%). Treatment of 1a, b with LiTMP/TMEDA in THF yields dilithio derivatives [Li(tmeda)]2[C6H4(CH)2BNR2] (8a, b) (40%) which show tripledecked structures consisting of an aromatic 10′-electron 2-benzoborole dianion and two [Li-(tmeda)]+ units facially bound to the borole ring. 1a reacts with HCl/Et2O/hexane to give C6H4(CH2)2BCl · OEt2 (1d · OEt2) (76%) which decomposes in vacuo to give the chloro derivative 1d. The methyl derivative C6H4(CH2)2BMe (1e) is obtained from 1a by treatment with LiMe/Et2O at -78°C and subsequently with HCl/Et2O at -78°C (41%). 1a, b react with MeOH at -78°C to give solid adducts C6H4(CH2)2BOMe · NHR2 (12a, b) while 1c affords C6H4(CH2)2BOMe (1f). Subsequent ring-opening produces 2-MeC6H4CH2B(OMe)2 (13). With the exception of 1b the 2-boraindanes 1 are crystalline solids. The silylation of the 2-benzoborole dianions and various (2-methylbenzyl)borane derivatives is also described.
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  • 89
    ISSN: 0009-2940
    Keywords: Cationic amido osmium(II) complexes, synthesis from dichloro metal precursor and primary amines ; Os-N double bond ; Aldimino(hydrido)osmium(II) complex, formation by β1-hydride migration ; Amino(chloro)osmium(II) complex, preparation by protonation of an amido derivate ; Dinuclear imidoosmium complex, presence of a Os2N2 four-membered ring ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbene-Type Amidoosmium Complexes with an Os—N Double Bond: Synthesis, Structure and Reactivity of [(Mes)Os(=NHR)(PiPr3)]PF6*The reaction of [(Mes)Os(PiPr3)Cl2] (1) (Mes=1,3,5-C6H3Me3) with primary amines RNH2 (R=Ph, Me, Et) in acetone/water (1:1) gives, after addition of KPF6, the amidoosmium(II) complexes [(Mes)Os(=NHR)(PiPr3)]PF6 (2-4) in 60-80% yield. From 1 and Et2NH, the chloro(hydrido)compound [(Mes)1-OsH(PiPr3)Cl] (5) is formed. The X-ray structural analysis of 2 reveals that the geometry around the osmium atom is trigonalplanar (with the midpoint of the mesitylene ring as one coordination site) and that the Os—N distance of 1.923(4) Å is in agreement with an Os—N double bond. Thermolysis of 4 (R=Et) at 165°C leads to the formation of the aldimino(hydrido)osmium complex [(Mes)OsH(NH=CHMe)(PiPr3)]PF6 (6) by β1-hydride migration from the NCH2 carbon atom to the metal atom. Protonation of 3 (R=Me) with HCl gives the amine complex [(Mes)Os(NH2Me)(PiPr3)Cl]PF6 (7), whereas on treatment of 3 and 4 with CD3NO2 the deuterated derivatives [(Mes)Os(=NDR)(PiPr3)]PF6 ([D1]-3, [D1]-4) are almost quantitatively formed. Compound 2 (R=Ph) reacts with KOtBu by proton abstraction and phosphane elimination to give the dinuclear imidoosmium complex [(Mes)2Os2(μ1-NPh)2] (8).
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  • 90
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1425-1427 
    ISSN: 0009-2940
    Keywords: Cope rearrangement ; Bullvalenes, pentabromo-and hexabromo- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Penta-and HexabromobullvalenesThe Pentabromobullvalenes 2a-d and the hexabromobullvalenes 3a/b are synthesized and the corresponding isomers are identified. 2 constitutes an equilibrium of four isomers. The isomer 2a is separated from the mixture by column chromatography. For the kinetically most stable isomer 2a the half-life time for equilibration at 55°C amounts to ca. 30 h. Two non-equilibrating isomers 3a and 3b are isolated, however, in the case of hexabromobullvalene 3. The bullvalene-typical property of a fluxional structure is now practically no longer existent.
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  • 91
    ISSN: 0009-2940
    Keywords: Supramolecular chemistry ; Crown ethers ; Phanes ; Fluid solutions and single crystals, spectroscopic properties of ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis and X-ray molecular structure of the title compound, an heptaoxa[3,13]paracyclophane, as well as that of its 1:1 sodium complex are described; a study of the absorption and fluorescence spectra indicates that this crown-cyclophane behaves as a hybrid between strained classical cyclophanes and large macrocycles.
    Additional Material: 7 Ill.
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  • 92
    ISSN: 0009-2940
    Keywords: Barbaralane, 2,6-diphenyl- ; Bicyclo[3.3.1]nona-2,6-diene, 2,6-diphenyl-, deprotonation of, by butylpotassium ; Bicyclo[3.3.1]nonadienediide, dipotassium, oxidation of, by 1,2-dibromoethane ; Reversed-phase liquid chromatography, preparative, of hydrocarbons ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The diphenylbicyclo[3.3.1]nonadiene 11 is deprotonated by butylpotassium to afford the black-red crystalline dipotassium diphenylbicyclo[3.3.1]nonadienediide 12. At low temperatures, 12 is oxidized in tetrahydrofuran solution by 1,2-dibromo-ethane yielding the diphenylbarbaralane 13 which is isolated in 57% yield on a 20-mmol scale after cyclic liquid chromatography on C18 reversed-phase silica gel with methanol. The packing procedure for suitable columns is also detailed.
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  • 93
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1493-1494 
    ISSN: 0009-2940
    Keywords: Phthalocyanine, tetravinyl- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of TetravinylphthalocyanineTetravinylphthalocyanine (5) has been prepared by heating 1,3-dihydro-1,3-diimino-5-vinyl-isoinodole (4) in DMAE. 5 is characterized by IR-, UV/Vis-, and 13C CP/MAS-NMR spectroscopy.
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  • 94
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    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1499-1502 
    ISSN: 0009-2940
    Keywords: α1-Cyanodiazonium ions ; α1-Cyanoalkyl radicals ; Carbocations, destabilized ; Substitution, nucleophilic ; Deamination reactions ; Diazonium ions ; Radicals ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Deamination Reaction, 54[1]. - Decomposition of 1-Cyano-1-propanediazonium IonsThe nitrous acid deamination of 2-aminobutanenitrile (9) was studied with regard to product distribution and stereochemistry. The formation of 2-(hydroxyimino)butanenitriles (21, 22; 8 - 28%) indicates the intervention of 1-cyanopropyl radicals (24) that are captured by NO. The polar reactions lead mainly to elimination (10 - 13) and nucleophilic substitution (14 - 16), rearrangement playing a minor role. (R)-9 was prepared from (R)1-2-aminobutanoic acid. The nitrous acid deamination of (R)-9 afforded the cyanohydrin 16 with 81% net inversion. Owing to destabilization of the carbocation 26 by CN, the SN2 route of nucleophilic displacement is preferred over SN1. The influence of CN is shown to be smaller than that of CF3.
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  • 95
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1519-1527 
    ISSN: 0009-2940
    Keywords: Cobalt(II), (η3-allyl)(η5-pentamethylcyclopentadienyl) complexes ; Cyclodimerisation and -trimerisation reactions ; Cycloaddition reactions ; Allyl-complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Reactivity of (η3-Allyl)(η5-pentamethylcyclopentadienyl)cobalt(II) and its DerivativesReaction of (η5-pentamethylcyclopentadienyl)cobalt(II) chloride (1) with allyllithium- or allylmagnesium compounds leads to new (η3-allyl)(η5-pentamethylcyclopentadienyl)cobalt(II) complexes 2a-d. Complexes 2a reacts with acetonitrile by oxidative addition of a methyl group to cobalt to form 5. With alkynes complexes with cyclodimerisized or -trimerisized alkynes as ligands are formed, e.g. the tetraphenylcyclobutadiene complex 6 from 2a and tolan and the hexamethylbenzene complex 8 from 2a and 2-butyne. Reaction with phenylethyne catalytically leads to triphenylbenzene 10. The complexes 2a-d are oxidized by iodine and bromine to Co(III) iodides 12a-d and bromides 14a and b and by ferricenium tetrafluoroborate to the tetrafluoroborates 13-c. The tetrafluoroborates give with nitriles stable complexes (nitrile-co-ordinated end-on to Co), with alkynes substituted cyclopentadienyl ligands coordinated to Co are formed by cycloaddition of the allyl group and the alkyne.
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  • 96
    ISSN: 0009-2940
    Keywords: Enantioselectivity ; Diels-Alder reactions ; Spiro-β1-lactones ; Retro cleavage ; Resolution, topological ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The racemic β1-isopropyl-α1-methylene-β1-lactone 1 undergoes a configuration-dependent, highly selective [4 + 2] cycloaddition to the enantiomerically pure cyclopentadiene 2; chromatographic separation of the adducts and subsequent thermal retro cleavage provide the pure enantiomers (S)-1 and (R)-1 in 99% e.e.
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  • 97
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    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1529-1531 
    ISSN: 0009-2940
    Keywords: [4 + 2] Cycloadditions ; Thiazyl compounds ; 1λ4,2-Thiazines ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: [4 + 2] Cycloadditions of Halogeno Thiazyls with 2-Chloropentafluoro-1,3-butadieneReactions of (XSN)n (n=3, 1; X=Cl, F) with 2-chloropentafluoro-1,3-butadiene provide the 1λ4,2-thiazines 1a and 1b. Fluorination with KF converts 1a in 88% yield to 1b. CH3OH reacts with 1b to form the 1-methoxy derivative 1c. The structure of 1c was determined by single-crystal X-ray diffraction analysis. With water 1a forms the 1,2-thiazin-3-one 1-oxide 2.
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  • 98
    ISSN: 0009-2940
    Keywords: Polylithium compounds ; NMR, 6Li ; Shift correlation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Sizable scalar 6Li,1H spin-spin coupling constants have been observed for the new dilithio compound (Z)-2-lithio-1-(o-lithiophenyl)ethene (3) which allow an assignment of the two non-equivalent 6Li resonance signals measured for the dimer of 3. Two-dimensional 6Li,1H shift correlation experiments based on multiple quantum spectroscopy as well as on polarization transfer are introduced as new tools for structural research in the field of organolithium compounds.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 99
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 2759-2763 
    ISSN: 0009-2940
    Keywords: Dichloroketene ; Stereoselective ketone reduction ; Mitsunobu reaction ; Cyclobutyl bromides ; Cross-coupling reaction ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Stereoselective Synthesis of 3-Substituted Cyclobutanols and Products Derived Therefrom3-Substituted cyclobutanones 2 are prepared by alkene/dichloroketene cycloadditions and subsequent dehalogenation. Reduction with LiAlH(OtBu)3 furnishes cis-cyclobutanols 3 in 95-100% selectivity. Mitsunobu inversion turned out to be the only practical method to get trans isomers 4 in high selectivity. A stereoselective cyclobutanol→bromocyclobutane conversion could be achieved only by a modified Mitsunobu reaction. Cross coupling between zinc derivatives of bromocyclobutanes 9 and aromatic bromides is not stereoselective.
    Additional Material: 1 Tab.
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  • 100
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1565-1569 
    ISSN: 0009-2940
    Keywords: Boranes, amino(imino)- ; Boranes, alkylidene(amino)- ; Tantalum, alkylidene complexes ; Azadiboracyclobutanes ; [2 + 2] Cycloadditions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Further Reactions of the Amino(imino)borane Me3Si(tBu)N*B*NtBu and the Alkylidene(amino)borane Me3Si(tBu)-N=B=CHtBuThe alkylidenetantalum complexes [tBuHC=TaCl3(THF)2] (1b), [PhHC=TaCl3(PMe3)2] (1c), and [tBuHC=Ta(CH2tBu)3] (1d) were treated with the amino(imino)borane Me3Si(t-Bu)N*B*NtBu (2d). From 1b and 2d, the alkylidene(amino)borane Me3Si(tBu)N=B=CHtBu (7) is formed by metathesis. The 1:2 reaction of 1c with 2d gives the azadiboracyclobutane [-N(tBu)-B(X)-CHPh-B(X)-] [6d, X=Me3Si(tBu)N]. The six-membered ring compound [-N(tBu)=BR-N(tBu)-SiMe2-CH2-TaR(CHtBu)-] (8, R=CH2tBu) is obtained from 1d and 2d; the product 8 crystallizes in the space group P 21/c. The borane 7 is attacked at the BC double bond by Et2NH, tBuCHO, and Me3SiN3 giving the diamino(neopentyl)borane 9 by protolysis, the oxaboracyclobutane 10 by [2 + 2] cycloaddition, and the azaboracyclopropane 11 by cycloaddition and elimination of N2, respectively.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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