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  • Artikel: DFG Deutsche Nationallizenzen  (2.391)
  • 1995-1999
  • 1990-1994  (2.391)
  • 1975-1979
  • 1970-1974
  • 1890-1899
  • 1994  (2.391)
  • Biochemistry and Biotechnology  (1.044)
  • Inorganic Chemistry  (688)
  • Atomic, Molecular and Optical Physics  (368)
  • Genetics  (291)
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  • Artikel: DFG Deutsche Nationallizenzen  (2.391)
Materialart
Erscheinungszeitraum
  • 1995-1999
  • 1990-1994  (2.391)
  • 1975-1979
  • 1970-1974
  • 1890-1899
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Schlagwörter
  • 201
    ISSN: 0009-2940
    Schlagwort(e): 1,2-Dithiines ; Thioindigo ; Thioketones ; Disulfides, cyclic, molecular structure and reactions ; Valence isomerization, electrocyclic ; Thiophenes, derivatives of ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Bis(benzo[4,5]thieno)[3,2-c:2′,3′-e][1,2]dithiin, ein Valenzisomer von „Dithioxo-thioindigo“3-Mercaptobenzo[b]thiophene (1) is transformed with assistance of bases, especially of amines, into the benzo[b]-thieno-annellated 1,2-dithiine 6 and not into the originally claimed “Dithioxo-thioindigo” trans-3. Primarily, the formation of 6 from 1 involves oxidation to the disulfide 4 which may also be used separately. Conceivable rationalizations are discussed. The same compound is accessible (in lower yield)by thionation of thioindigo with the aid of the Lawesson reagent. X-ray elucidation of 6 reveals a non-planar structure of the cyclic disulfide with a dihedral C—S—S—C-angle of 53°. Despite of the absence of any established chromonphoric moiety, 6 is deeply red in the crystal and in solution, as it is representative for the “undisturbed” 1,2-dithiine system. Contrary to the usual behaviour of the non-annellated 1,2-dithiines, 6 displays no spontaneous sulfur extrusion under mild conditions, but only at high temperatures and in the presence of sulfur-binding agents, leading to the benzo[b]thieno-annellated thiophene 22. Moreover, 6 may be reduced to the dithiol 14 (or 13, respectively) and regenerated exclusively from this by oxidation. Further characteristic reactions of 6 are described (e.g. to the sulfoxide 18, to the pyridazine 19, and to the thiphosphoric ester 21).
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 202
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 445-445 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 203
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 449-455 
    ISSN: 0009-2940
    Schlagwort(e): Trifluoromethylsulfanyl compounds ; Pentafluorophenylsulfanyl compounds ; Trifluoromethylselenanyl compounds ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Tris(perfluoroorganochalkogenyl)methyl Compounds: Synthesis, Structures, and PropertiesReaction of (CF3S)2CHC(OC2H5)3 with CF3SCl or CF3SeCl in the presence of NaH in ether provides X(CF3S)2CC(O)OC2H5 (1a, b: X = CF3S, CF3Se). These compounds react with NH3 to form (CF3S)2CHC(O)NH2 (2b) which is also obtained from (CF3S)2CHC(O)OC2H5 and NH3. Dehydration of the amide 2b yields (CF3S)2CHCN (3b), which reacts with NaH and then with CF3SX (X = Cl, SCF3) or with RfCl (Rf = CF3Se, C6F5S) to give Rf (CF3S)2CCN [Rf = CF3S (3c), CF3Se (3d), C6F5S (3e)]. 3c is also obtained from (CF3S)3CBr and AgCN. Hydrolysis of 3c with conc. H2SO4 leads almost quantitatively to (CF3S)3CC(O)NH2 (2c), which on treatment with COCl2 gives only 3c and not the corresponding isocyanate. If phosgene is replaced by oxalyl chloride and treated with 2c in a 1:1 molar ratio, (CF3S)3CC(O)NCO (4a) is formed. The urea derivative (CF3S)3CC(O)NHC(O)NHC(O)C(SCF3)3 (4b) is obtained either by using a 2:1 molar ratio of 2c and [C(O)Cl]2 or from 2c and 4a. Attempts to substitute (CF3S)2CHCO2H - after treatment with NaH in ether - with CF3SCl provides low yields of 2,4-bis[bis(trifluoromethylsulfanyl)methylene]-1,3-dithietane (5). X-ray structure analyses are performed for (CF3S)3CCN (3c) and the 1,3-dithietane 5.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 204
    ISSN: 0009-2940
    Schlagwort(e): 2-Pyridylalkylphosphanes ; Hemilabile ligands ; Nickel complexes ; Palladium complexes ; Platinum complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Synthesis and Coordination Chemistry of Hemilabile P,N-Hybride Ligands with Terminal 2-Pyridyl Donor Groups*P,N-hybride ligands 1-7 containing terminal 2-pyridyl donor groups have been obtained by base-catalyzed addition of diphenylvinylphosphane or 2-vinylpyridine to primary or secondary phosphanes [2-Py-(CH2)2-PR′H (R′ = H, Ph), HMeP-(CH2)3-PMeH] or by alkylation of organolithium phosphides, R2P-(CH2)3-PMeLi or 2-Py-(CH2)2-PR′Li (R = Ph, iPr; R′ = H, Ph), with 2-(2-chloroethyl)pyridine or di-tert-butylphosphetanium bromide. Upon reaction with NiBr2 3 H2O or K2MCl4 (M = Pd, Pt) the phosphanes (L) of type 2-Py-(CH2)2-P(R′)-(CH2)m-PR2 (1, 3, 6) form square planar Ni(II), Pd(II), and Pt(II) complexes of composition MX2(L) (10-14). With NiBr2 and K2MX4 the tripod type phosphane 2 forms square pyramidal complexes [MX(2)]X (M = Ni, Pd; X = Cl, Br; 15, 16). An X-ray structural analysis of [NiBr(2)]+Br- (15) reveals a distorted square pyramidal coordination geometry at Ni(II), the 2-Py donor being in apical position with a long Ni—N bond [2.270(15) Å]. The tetradentate ligand 7 forms Ni(II), Pd(II), and Pt(II) complexes MX2(7) which for M = Pd, Pt show dynamic behaviour by exchange of the terminal Py donor groups. With [RhCl(COD)]2 the tridentate ligands L (1 and 3) yield complexes of composition RhCl(L) (20, 21). The structure of 20 has been determinated by X-ray diffraction. The ligand 3, acting in a tridentate manner, is coordinated to Rh(I) in a distorted square-planar arrangement with a normal Rh—N distance [2.145(3) Å].
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 205
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 519-523 
    ISSN: 0009-2940
    Schlagwort(e): Calixarenes ; Friedel-Crafts reaction ; selective ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The para-acylation of calix[4]arene (2), calix[6]arene (3), and calix[8]arene (4) by Friedel-Crafts reaction with a wide variety of acyl chlorides leads to 5-7 in moderate to good yields. Friedel-Crafts reaction of 26,28-dimethoxycalix[4]arene (8) gave products 9 selectively disubstituted in the para-positions of phenol rings.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
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  • 206
    ISSN: 0009-2940
    Schlagwort(e): Radicals ; Cyclization ; Triquinanes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Radical-Type Cyclization of Dienes, VIII[1].  -  On the Regioselective Synthesis of Unsaturated Cyclopenta[b]furan-2-ones from (S)-(+)-Carvone  -  Building Blocks for the Synthesis of Enantiomerically Pure TriquinanesThe diastereomeric products 2a and 2b, which were synthesized from (S)-(+)-carvone (1), are converted to (3aS,5S,6aS)-(-)-5-acetoxyhexahydro-6a-methyl-2H-cyclopenta[b]furan-2-one (4) in ca. 50% yield. 4 is regioselectively converted to (3aR,6aS)-(-)-3,3a,6,6a-tetrahydro-6a-methyl- (8a) and (3aS,6aR)-(+)-3,3a,4,6a-tetrahydro-6a-methyl-2H-cyclopenta[b]-furan-2-one (8b). These are used at the 10-g scale for the synthesis of enantiomerically pure triquinanes.
    Materialart: Digitale Medien
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  • 207
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 585-585 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 208
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 597-603 
    ISSN: 0009-2940
    Schlagwort(e): (Trifluoromethylthio)carbon ; Carbenium ions ; One-electron oxidation ; Superacidic systems ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Syntheses and Reactions of Fluoroorganic Acyclic Thiocarbenium IonsHerrn Prof. Dr. W. Sawodny zum 60. Geburtstag gewidmet.Arsenic pentafluoride oxidizes (F3CS)4C (1) but not (F3CS)2C = C(SCF3)2 (2) to yield the stable salt (F3CS)3C+AsF-6 (3). It reacts with halide ions to form (F3CS)3CX (3a-c, X = F, Cl, Br). Iodide is oxidized to iodine with formation of (F3CS)3CC(SCF3)3 (4) which reacts with nitrogen dioxide to give (F3CS)3CNO2 (3e). - (F3CS)3C+AsF-6 (3) removes from (F)-SCF3 (5a) a ring-bound fluorine atom to afford (F3CS)3CF and -SCF3]+AsF-6 (5). When (F3CS)3CCl (3b) is treated with AsF5, 3 and [(F3CS)2-CCl]+AsF-6 (6) are formed in a 2:1 molar ratio. The latter reacts with F- or Cl- to give (F3CS)2CClX (6a,b; X = F, Cl). AsF5 is capable of abstracting a fluoride ion from (F3CS)3 - n Cln,CF only if n = 0 or 1. For n = 2 no similar reaction takes place, but with AlCl3 in BCl3 halogen exchange to F3CSCCl3 (7b) is observed. - Alkylation of (F3CS)2C=S (8) with H3CF/AsF5 yields [(F3CS)2CSCH3]+AsF-6 (9), which adds a fluoride ion to give (F3CS)2(H3CS)CF (9a). The molecular structures of (F3CS)2C = C(SCF3)2 (2) and (F3CS)3CC(SCF3)3 (4) have been determined by X-ray diffraction methods.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 209
    ISSN: 0009-2940
    Schlagwort(e): Ruthenium complexes ; Osmium complex ; Hydrido complexes ; α-Amino acids ; Oxidative Addition ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Metal Complexes of Biologically Important Ligands, LXX[1].- Synthesis, Stereochemistry and Reactions of Ruthenium(II) and Osmium(II) Complexes with α-Amino CarboxylatesHerrn Professor Helmut Werner zum 60. Geburtstag gewidmet.The reactions of MHCl(CO)(PPh3)3 with salts of α-amino acids give the hydrido-N,O-chelate complexes MH(CO)(NH2CHR-COO)(PPh3)2 (1a-g;) M = Ru, Os). Complexes 1a-c can alternatively be prepared by oxidative addition of the appropriate α-amino acid to Ru(CO)3(PPh3)2. The crystal structure of 1b has been determined by an X-ray structural analysis. The leucinato compound 1c is an effective catalyst for the decomposition of formic acid. In contrast, reactions of RuHCl-(CO)(PPh3)3 with α-amino acids afford the chloro-N,O-che-late complexes RuCl(CO)(NH2CHRCOO)(PPh3)2 2a-h. The decomposition reactions of 2c, 2g and2h have been investigated.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 210
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 643-646 
    ISSN: 0009-2940
    Schlagwort(e): λ5-Germanate, zwitterionic ; Germanium, pentacoordinate ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The zwitterionic spirocyclic λ5-germanate bis[2,3-naphthalenediolato(2 - )](pyrrolidiniomethyl)germanate (8) was synthesized and the crystal structure of its tetartoacetonitrile solvate 8 · 1/4 CH3CN studied by single-crystal X-ray diffraction. Compound 8 was prepared by reaction of (MeO)3-GeCH2NC4H8 (11; NC4H8 = pyrrolidino) with two equivalents of 2,3-naphthalenediol (isolated as 8 · 1/4 CH3CN; yield 92%). The coordination polyhedron around the pentacoordinate germanium atom of 8 · 1/4 CH3CN can be described as a strongly distorted trigonal bipyramid (the structure is displaced by 38.9% from the ideal trigonal bipyramid towards the ideal square pyramid), the carbon atom occupying an equatorial position. In the crystal lattice of 8 · 1/4 CH3CN, the zwitterions form intermolecular N—H⃛O hydrogen bonds leading to the formation of dimers. 1H- and 13C—NMR studies revealed that 8 also exists in solution ([D6]DMSO).
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 211
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 673-675 
    ISSN: 0009-2940
    Schlagwort(e): Radicals ; Addition ; Alkynes ; Kinetics ; Supercritical fluid conditions ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The kinetics of the addition of cyclohexane (2) to phenylethyne (1) proceeding via 2-cyclohexyl-1-phenylethenyl radical (3) to give 1-cyclohexyl-2-phenylethene (4) was investigated in the temperature range from 260 to 340°C. The radical chain is initiated by a bimolecular reaction of cyclohexane with phenylethyne to give a cyclohexyl radical and a 1-phenylethenyl radical. The physical state of the reaction mixture was varied from liquid to supercritical and to gasphase conditions. No effect on the reaction rate constant near the critical point was observed.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 212
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 685-689 
    ISSN: 0009-2940
    Schlagwort(e): 1,2-Oxazines ; Bromination, radical ; SN2 reaction ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 5,6-Dihydro-4H-1,2-oxazines 1a-b, 2, and 3 are easily brominated at C-4 with N-bromosuccinimide/dibenzoyl peroxide in tetrachloromethane. The bromo substituent is incorporated with surprisingly high diastereoselectivity trans to the substituent at C-6. 4-Bromo-5,6-dihydro-4H-1,2-oxazines are useful reagents for substitution reactions with N-nucleophiles such as primary amines and azide ions. Inversion of configuration at C-4 provides derivatives of 4-amino-1,2-oxazines with uniform relative configuration. As a minor byproduct the dibromo adduct 7 is obtained by bromination of 3. The dehydrohalogenation of this compound allows the synthesis of the 4-bromo-6H-1,2-oxazine 12. The presented reaction sequence thus constitutes an “umpolung” reaction that allows the introduction of nucleophiles into a position of the oxazine ring that so far was accessible only for electrophiles. The diastereoselectivity of the bromination reaction is discussed.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
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  • 213
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994) 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 214
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 821-824 
    ISSN: 0009-2940
    Schlagwort(e): Alkoxide complexes ; Manganese complexes ; Iron complexes ; Cobalt complexes ; Zinc complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Volatile Metal Alkoxides According to the Concept of Donor-Functionalized LigandsHomoleptic metal(II) alkoxides 3-5 of manganese, iron, cobalt, and zinc are prepared by applying the concept of donor-functionalized ligands. The trifunctional ether ligands 1 thus form volatile metal alkoxides that sublime below 100°C at 10-2 mbar. Monomeric molecules are present in the gas phase and are likely to occur in the solid state, too. The heterodimetallic alkoxide 6 (Li/Co) sublimes without decomposition.
    Materialart: Digitale Medien
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  • 215
    ISSN: 0009-2940
    Schlagwort(e): Silver(I) complexes ; Bis(diphenylphosphanyl)-o-carborane ; o-Carborane ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Silver(I) perchlorate or nitrate react readily with bis(di-phenylphosphanyl)-o-carborane to give the complexes [AgX{(PPh2)2C2B10H10}] [X = ClO4 (1), NO3, (2)]. The perchlorate ligand is weakly bound to the silver atom and thus can be displaced by other ligands affording the three-coordinated complexes [AgL{(PPh2)2C2B10H10}]ClO4 [L = PPh3 (3), PPh2Me (4), AsPh3 (5), C5H4NCOOH (6), C9H6NCOOH (7), SPPh3 (8)]. Compounds 3 and 4 can also be obtained by reaction of [Ag(OClO3)PR3] with the diphosphane. Treatment of complex 1 with bidentate ligands leads to the cationic four-coordinated [Ag(L—L){(PPh2)2C2B10H10}]ClO4 [L—L = (PPh2)2C2B10H10 (9), bipy (10), phen (11), (SPPh2)2CH2 (12)] or to the neutral [Ag(S2CNR2){(PPh2)2C2B10H10}] [NR2 = NEt2 (13), NC4H8 (14)]. The crystal structures of 11 and 12 have been established by X-ray crystallography. In both complexes the silver(I) atoms exhibit tetrahedral coordination by two phosphorus and two nitrogen or two sulfur atoms, respectively.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 216
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 853-855 
    ISSN: 0009-2940
    Schlagwort(e): Diethylamine - arachno-nonaborane ; Diethylamine - octadecaborane ; conjuncto-Bis[6′5′:5,6]decaborane ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: On the Thermolysis of Amine-arachno-NonaboraneTwo molecules of diethylamine-arachno-nonaborane, B9H13-(NHEt2), undergo a condensation at 140°C to give diethylamine-conjuncto-bis[6′,5′:5,6]decaborane, B18H20(NHEt2) (4). The deprotonation of 4 yields the anion [B18H19(NHEt2)]-which can be crystallized with the cation [NEt3(CH2Ph)]+ (space group P1).
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 217
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 875-879 
    ISSN: 0009-2940
    Schlagwort(e): [2.2]Paracyclophanes ; Electron transfer reactions ; Radicals ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Single electron transfer (SET) oxidation of [2.2]paracyclophane (1) with cerium ammonium nitrate (CAN) produces the corresponding radical cation (1+.), which undergoes cleavage of the carbon-carbon bond of the ethano bridge to generate the double-benzylic radical cation 2+. Trapping of this intermediate by oxygen and nucleophiles gives rise to aldehydes 3, while a second oxidation and subsequent nucleophilic trapping affords nitrates 4. This facile cleavage of the carbon-carbon bond is explained by alignment of the latter with the π systems in the rigid structure of [2.2]paracyclophane, which enables charge delocalization across both benzene rings. When the reaction is carried out in methanol, aromatic substitution takes also place as a minor reaction pathway, which is responsible for the formation of the polyfunctionalized cyclophane 5d.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 218
    ISSN: 0009-2940
    Schlagwort(e): Chromium, [2-(methyleneamino)ethenyl]carbene complexes ; Michael addition of imines ; (1-alkynylcarbene)-chromium complexes ; 2H-Pyrroles ; Cyclization of {[2-(methyleneamino)ethenyl]carbene}chromium complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Imines 7, 11-13 were added to (1-alkynylcarbene)chromium complexes 6a-d to form {[2-(methyleneamino)ethenyl]-carbene}chromium complexes 8a-d, 14a-d, 15a-d, 16a-d in good to very good yields (63-98%) except for two cases (41-59%). The carbene ligands of the latter compounds cyclize to 2H-pyrroles 9a-d, 17a-d, 18a-d, 19a-d upon heating in tetrahydrofuran solution to 50-55°C.
    Zusätzliches Material: 4 Tab.
    Materialart: Digitale Medien
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  • 219
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A53 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 220
    ISSN: 0009-2940
    Schlagwort(e): Diphosphaallenes ; 1H-Diphosphirenes ; 3H-Diphosphirenes ; Phosphanylphosphaalkynes ; Calculations ; ab initio MO ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Ab initio MO calculations at the QCISD(T)/6-31G* */MP2/6-31G* * + ZPE level on the XX′CP2 isomers (X = H1 F and Cl) show that the energies of the isomeric species are often reordered following halogen substitution. The phosphorushalogen moiety behaves as the main stabilizing factor on the rest of the molecular structure. This is particularly true when X = F is involved. In the dihalogenated series phosphanyl-phosphaalkyne (4) becomes the most stable species followed by diphosphaallene (3) and 1 H-diphosphirene (6). The effect on the geometry following halogenation is larger if substitution takes place at carbon than at phosphorus. The behaviour of the P species is found to be quite different from, if not opposite to, that of their nitrogen analogues. Finally, the infrared spectra of the most stable isomers are also predicted.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 221
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2381-2385 
    ISSN: 0009-2940
    Schlagwort(e): Zinc complexes ; Pyrazolylborate ligands ; Drugs as ligands ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Pyrazolylborate-Zinc Complexes with Drugs as LigandsThe model complexes for hydrolytic zinc enzymes L3Zn-OH with L3a = tris(3-tert-butyl-5-methylpyrazolyl)borate and L3b = tris(3-cumyl-5-methylpyrazolyl)borate (1a, b) were tested for their interaction with drugs. With acetazolamide (HAcm) the complex L3bZn-Acm (2b) is obtained which according to a structure determination contains the Acm ligand chelating by one azole and the sulfonamide nitrogen atoms. Furosemide (HFur) forms the two complexes L3Zn-Fur (3) which according to their spectra contain the furosemide anion as a monodentate carboxylate ligand. Aspirin (AcSalH) is saponified by both L3Zn-OH complexes yielding L3Zn-Sal (4). The structure determination of L3bZn-Sal (4b) has shown the salicylic acid to be bound as a monodentate carboxylate as well.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 222
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2417-2419 
    ISSN: 0009-2940
    Schlagwort(e): Epoxides, optically pure ; Zirconocenes, enantiomerically pure ; Octahydrofluorenyl ligands ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Ring opening of (R)-(-)-epoxystyrene (1) with fluorenyllithium leads to the optically active alcohol 2 in high yield. Derivatization of 2 to the trifluoromethanesulfonate 4 and subsequent reaction with one equivalent of fluorenyllithium gives the ligand precursor (1S)-1,2-bis(9-fluorenyl)-1-phenylethane (5), which is used for the synthesis of [(1R)-1,2-bis(η5-9-fluorenyl)-1-phenylethane]ZrCl2 (6).
    Materialart: Digitale Medien
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  • 223
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2431-2433 
    ISSN: 0009-2940
    Schlagwort(e): Protonation, regioselective ; Allyllithium compound ; Allyl anion ; General acid ; Regioselectivity ; Aging ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: By varying the general acid, the regioselectivity of the protonation of (triphenylsilyl)allyllithium (1) in diethyl ether in the presence of HMPT can be changed from 9:1 to 1:9 at room temperature. When other aprotic solvents are used, the nature of the lithium salt changes, and the selectivity decreases. The regioselectivity of the protonation of the dithio-stabilized allyllithium 4 by water is highly dependent on the age of the allyllithium solution with α/γ ratios varying from 2.7:1 to 1:3.5.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 224
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1219-1221 
    ISSN: 0009-2940
    Schlagwort(e): Tetrasulfane, bis(2,3,4,6-tetra-O-acetyl-1-deoxy-β-D-glucopyranosyl)- ; Undecasulfane, bis(2,3,4,6-tetra-O-acetyl-1-deoxy-β-D-glucopyranosyl)- ; Polysulfanes, bisorganyl ; Sulfanes, dialkoxy- ; 1-Thio-β-D-glucopyranose, tetra-O-acetyl- ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Dialkoxysulfanes (RO)2Sn (n ≥ 2) react with thiols R′SH as sulfur transfer reagents to form long-chain diorganylpoly-sulfanes R′2Sn+2 under mild conditions. Condensation of tetra-O-acetyl-1-thio-β-D-glucopyranose (acGlcSH) with diisopropoxydisulfane (iPrO)2S2 and diisopropoxynonasulfane (iPrO)2S9 at 40°C yields bis(2,3,4,6-tetra-O-acetyl-1-deoxy-β-D-glucopyranosyl)tetrasulfane (1) (acGlc)2S4 and bis(2,3,4,6-tetra-O-acetyl-1-deoxy-β-D -glucopyranosyl)undecasulfane (2) (acGlc)2S11, respectively. The analogous reaction using diisopropoxymonosulfane does not yield the corresponding trisulfane.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 225
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1223-1233 
    ISSN: 0009-2940
    Schlagwort(e): Cysteine derivatives ; Zinc complexes ; Constitution and structure ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Zinc Complexes of Amino Acids and Peptides, 3[1]. - Zinc Complexes of Peptides with N-terminal CysteineConventional methods were used to prepare three dipeptides Cys-X-OR (X = Gly, Phe), nine dipeptides Cys-X-NH2 (X = Gly, Ala, Val, Leu, Ile, Pro, Phe, Met, Ser), three tripeptides Cys-X-OR (X = Gly-Gly, Phe-Phe, Met-Phe), and three tripeptides Cys-X-NH2 (X = Gly-Gly, Gly-Ala, Gly-Leu). All these peptides have the unprotected amino acid cysteine at the N terminus. Their reactions with basic zinc carbonate resulted in the formation of mononuclear complexes ZnL2, with L being the peptide anion resulting from SH deprotonation, IR and NMR spectra indicate that in all these complexes the zinc ion is coordinated by the cysteine thiolate and amino functions of two peptide ligands. This tetrahedral ZnN2S2 coordination by two chelating peptides is confirmed by a crystal structure determination of the complex Zn(Cys-Gly-NH2)2.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 226
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1235-1241 
    ISSN: 0009-2940
    Schlagwort(e): Cysteine derivatives ; Zinc complexes ; Solution equilibria ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Zinc Complexes of Amino Acids and Peptides, 4. - Zinc Complexes of Peptides with C-terminal CysteineThe cysteine derivatives N-Ac-Cys, N-Ac-Gly-Cys, N-Ac-Ala-Cys, and N-Ac-Gly-Gly-Cys with unprotected SH and CO2H functions (LH2) were prepared by the mixed anhydride method. Their reactions with basic zinc carbonate resulted in the formation of complexes Zn(LH)2 which were converted by KOH to complexes K2[ZnL2]. Potentiometric titrations revealed ZnL and [ZnL2]2- as the major solution species. By pD-dependent NMR measurements (1H, 13C) in D2O carboxylate coordination in acidic solution and carboxylate and thiolate coordination in neutral and basic solution was identified.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 227
    ISSN: 0009-2940
    Schlagwort(e): η1-Allyl iron complexes ; 1,3-Dipolar cycloaddition ; Nitrile oxides ; Isoxazolines ; Diastereoselective synthesis ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Cycloadditions of Organometal Fragment-Substituted Alkenes, I. - [3 + 2] Cycloaddition of η1-Allyl Iron Complexes with Nitrile Oxides: Ferriomethyl-Substituted IsoxazolinesThe isoxazolines C5H5(OC)(L)Fe-CH2-CH-CH2-C(R) = N-O (3a-f) [R = Ph, 2,4,6-Me3C6H2; L = CO, P(OCH2)3CCH3, PPh3], substituted with a ferriomethyl group in 5-position, are obtained by 1,3-dipolar cycloaddition of the η1-allyliron complexes C5H5(OC)(L)Fe-CH2-CH=CH2 [L = CO (1a), P(OCH2)3CCH3 (1b), PPh3 (1c)] with the nitrile oxides RCNO [R = Ph (2a), Mst (2b)]. The chiral complexes 1b, c produce the diastereomeric isoxazolines 3b, c, e, f with diastereomer ratios of 59:41 to 93:7. The structure of 3d is established by crystal structure analysis.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 228
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1251-1253 
    ISSN: 0009-2940
    Schlagwort(e): Coronene(1-), radical anion ; Potassium compounds ; Graphite model studies ; Calculations, MNDO ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Crystallization of potassium(1+) and the radical ion coronene(1-) from a mixture of tetramethylethylenediamine (tmeda), tetrahydrofuran (THF), and diethyl ether yields a monomeric solvated ion pair 1 with potassium unsymmetrically π-coordinated to an external ring of the polyaromatic system according to an X-ray structure determination and in agreement with a MNDO theoretical investigation.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 229
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1257-1262 
    ISSN: 0009-2940
    Schlagwort(e): Electrochemistry ; Oxidation, anodic ; CH Acids ; Dehydromerization ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Oxidative Dimerization of CH AcidsAnodic oxidation of alkyl- (1) and acylmalonic acid esters (7) yields the dehydromiers 4 and 8, respectively. Preparative electrolyses are performed in acetonitrile in the presence of a base to generate the carbanion corresponding to the CH acid. The carbanions are oxidized to the radicals which dimerise on the electrode surface. The yields of the preparative electrolyses and the formation of the dehydrodimers 4 and 8 are discussed in terms of the CH acidity and enolization of starting materials.
    Zusätzliches Material: 8 Tab.
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  • 230
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1247-1249 
    ISSN: 0009-2940
    Schlagwort(e): 1,5,2,4-Diazadiphosphorinane-6-one, cis-trans isomerism of ; 1,5,2,4-Diazadiphosphorinan-6-one, 2,4-disulfides ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The 2,4-bis(dialkylamino)-1,5-dimethyl-1,5,2,4-diazadiphos-phorinan-6-ones 1a and 1b (R = CH3, a; C2H5, b) are thermally unstable and are transformed into the bicyclic species 2 when heated to 150°C (2 Torr). The reactions of 1a and 1b with elemental sulfur lead to the P,P′-disulfides 4a and 4b as a mixture of cis and trans isomers which are separated by column chromatography. Single-crystal X-ray structure determinations were conducted on compound 2 and on the cis and trans isomers of 4b. The bicyclic compound 2 is found to display crystallographic twofold symmetry. Its structure is closely similar to that of the diphenyl analogue. For the cis and trans isomers of 4 almost ideal S-P…P-S torsion angles are observed. The isomers adopt different ring conformations.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 231
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    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1263-1267 
    ISSN: 0009-2940
    Schlagwort(e): Photochemistry ; Stereoselective bromination ; Deoxygenation ; Allyl-Cyclopropyl ring closure ; 2D-NMR ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Synthesis of Medium and Large Rings, XXXVI.  -  Synthesis of a Bridged Bicyclo[2.1.0]pentane Derivative with inside ConfigurationDihydrocyclobutafurans 4 (H instead of Br) are reactive intermediates in the photochemical rearrangement of 3,6-hexanooxepine-4,5-dicarboxylic esters. The synthesis of the bromo derivative 4 was achieved by irradiation of the epoxyoxepine 1 followed by a regio- and stereoselective NBS bromination of 2 and deoxygenation of 3 with tungsten hexachloride/n-butyllithium. Treatment of the allylic bromide 4 with sodium methoxide gave surprisingly the title compound 5. The structure of 5 was established by thorough NMR analysis.
    Zusätzliches Material: 1 Ill.
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  • 232
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1275-1281 
    ISSN: 0009-2940
    Schlagwort(e): Ketenes (dimeric) ; reactions with nucleophiles and electrophiles ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The title lactone 2 acylates a variety of amines including phenylalanine, sterically hindered alcohols, and phenols. With activated non-enolizable carbonyl compounds, bis-spiro 6-membered β-keto lactones are formed. Oxidative rearrangement of 2 affords bis-spiro lactones 12 and 13.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 233
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1269-1274 
    ISSN: 0009-2940
    Schlagwort(e): Ketene cycloadditions ; Cycloheptadienones ; Carbocations ; Rearrangements ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reaction of ketenes 1a or 1b with diene 2 in the presence of trifluoromethanesulfonic acid providing the cycloheptadienones 5a and 5b constitutes the first example of an acid-induced ketene/diene «cycloaddition». The thermal [2 + 2] cycloadducts, bicyclo[3.2.0]hept-2-en-6-ones 9, are not intermediates in the acid-catalyzed reaction since they rearrange under acidic conditions to the tetralinone derivatives 10. The acid-catalyzed «cycloaddition» was mechanistically investigated and the scope of the reaction explored.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 234
    ISSN: 0009-2940
    Schlagwort(e): (Aminomethylene)cyanoacetate, ethyl, derivatives ; Coordination polymers, 1D ; Self-organization, spontaneous ; Copper complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Reaction of a solution of copper(II) acetate in methanol with ethyl (aminomethylene)cyanoacetate derivatives 10 (H2L4) or 13 (H2L5) yields the corresponding 1D-coordination polymers 11 ([CuL4]∞ and 14 ([CuL5]∞, respectively. The products are insoluble in non-coordinating solvents and thermally highly stable. The structures of 11 and 14 have been established by X-ray diffraction. The one-dimensional coordination polymers 11 and 14 have different geometries, depending on the lateral group of the ligands.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 235
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1295-1303 
    ISSN: 0009-2940
    Schlagwort(e): Imines ; Iminium salts ; 3-Trifloxypropeniminium salts ; Propyniminium salts ; Cyclization reactions ; Azacyclobutadiene ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The imines 5 and 11 react with 3-trifloxypropeniminium triflates 1a-d to afford the heterocyclic iminium salts 8, 9, 13, 15, and 17, respectively, or the propeniminium salt 21. Propyniminium triflates 22, 24 react with imines by initial conjugated addition, followed by a reaction sequence analogous to the one observed for the reactions of 1a-d with imines. Thus, salt 22 and aldimine 5b yield the propeniminium salt 21, while 24 reacts with tri-tert-butylazete 25 to afford the semicyclic vinamidinium salt 28. A crystal structure analysis of 28 is performed.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 236
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1287-1293 
    ISSN: 0009-2940
    Schlagwort(e): Ynamines, N,N-bis(trimethylsilyl)- ; Cycloaddition reactions ; Cyclopropenes ; Furans ; Ketenes ; Cyclobutenones ; Allenylcarboxamides ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: N,N-Bis(trimethylsilyl)ynamines 1 react with dimethyl acetylenedicarboxylate (2) in a molar ratio of 1:2 to afford 3-cyclopropenylfurans 3. Configuration and conformation of 3a are confirmed by X-ray crystallography. Addition of a further mol of 1 furnishes the fumarates 4. With ketenes 5 (5c, d are prepared in situ) a competition between the formation of cyclic butenone derivatives 6 and allenic imidates 7 is observed, depending on the substitution pattern of 1. After hydrolytic workup, the corresponding amides 10 or the vinylogous amides 9 are obtained in good yield. These experiments indicate that the silylated ynamines 1 show a completely different, more selective reactivity towards dimethyl acetylenedicarboxylate compared to N,N-dialkyl-substituted ynamines, yielding furan derivatives instead of anilines. Towards ketenes, however, a similar cycloaddition reactivity as for N,N-dialkylynamines is observed.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 237
    ISSN: 0009-2940
    Schlagwort(e): Radicals ; Cyclobutanes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Radical-Type Cyclization of Dienes, IX. - On the Stereoselectivity of the Radical 4-exo-trig-Cyclization of Optically Active Ethyl (2E)-6-Oxohex-2-enoates with Samarium(II) IodideEthyl (5R, 2E)-5-(benzyloxy)-4,4-dimethyl-6-oxohex-2-enoate (9) was prepared from (R)-(-)-pantolactone (3) by a series of straightforward reactions. The reaction of 9 with samarium(II) iodide produces enantiomerically pure ethyl (1S,3R,4R)-(-)-[3-(benzyloxy)-4-hydroxy-2,2-dimethylcyclo-butyl]acetate (10) in 60% yield. The absolute configuration at C-1 and C-3 was confirmed by the conversion of 10 to the crystalline 15a, whose absolute configuration is known from its synthesis from (1S,5S)-( + )-α-pinene (12). The configuration of the hydroxy group at C-4 in 10 was determined from NOE studies on the epimiric 17. The radical 4-exo-trig-cyclization of optically active (2E)-6-oxohex-2-enoates with samarium(II) iodide opens a new pathway to enantiomerically pure cyclobutanol and cyclobutanone derivatives, which are of interest as building blocks in natural products synthesis.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 238
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1311-1316 
    ISSN: 0009-2940
    Schlagwort(e): 1-Iodoalkylmagnesium reagents ; Stability, configurational ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: α-Iodoalkylmagnesium species were generated by reaction of 3-oxygenated 1,1-diiodoalkanes with isopropylmagnesium halides at -78%C. The resulting magnesium carbenoids were found to be configurationally stable at temperatures up to -20%C and were trapped by benzaldehyde or allyl iodide at low temperatures. Stereoselectivity on exchange of the diastereotopic iodine atoms in 3 was found to be low.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 239
    ISSN: 0009-2940
    Schlagwort(e): Allylamine nickel complexes ; Allylamine cobalt complexes ; 2D NMR, TOCSY ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 16-Electron complexes of zerovalent nickel with diallylamines, Ni[(C3H5)2NR]L [1, 2: L = P(CH3)3, R = CH3, C6H5; 3: L = P(C6H5)3, R = CH3] and [NiP(CH3)3]2CH2[N(C3H5)2]2 (4), were synthesized by reduction of NiCl2L2 with magnesium in tetrahydrofuran. NiCl(η3-C3H5)[P(CH3)3]2 (5), a low-yield byproduct, was also obtained in high yield from NiL4 and C3H5Cl. With triallylamine as starting material complexes Ni[(C3H5)3N]L [6: L = P(CH3)3; 7: L = P(C6H5)3] were generated exhibiting η6- and η4-olefin coordination, respectively. 17-electron cobalt(O) compounds Co[(C3H5)2NR](PMe3)2 (8, 9: R = CH3, C6H5) were obtained by reaction of Co(cyclo-C5H8)(PMe3)3 with the corresponding diallylamine, while CoR(PMe3)4 (R = CH3, C6H5) reacted with N,N-diallylaniline to give diagmagnetic Co[(η3-C3H4)(η2-C3H5)NC6H5](PMe3)2, (10). The coordination mode of allylic functions was deduced from IR, ESR and especially 1H- and 13C-NMR spectra including 2D-NMR experiments.
    Zusätzliches Material: 1 Ill.
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  • 240
    ISSN: 0009-2940
    Schlagwort(e): Alkynylnickel halides ; Nickel complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Oxidative Linear Trimerization of Alkynyl Groups in (Trimethylphosphane)nickel Complexes: Structures and the Role of Ligand-Rich Precursors NiX(C≡CR)(PMe3)n (n = 2-4)Oxidative additions of 1-halogenoalkynes XC≡CR; to Ni(PMe3)4 afford high yields of pentacoordinate ionic alkynylnickel compounds [Ni(C≡CR)(PMe3)4]+X- [R = SiMe3, X = I (1); R = CMe3, X = I (2), Br (3); R = SiEt3, X = I (6), Br (7); R = SiiPr3, X = I (10), Br (11), R = Ph, X = I (21), Br (22)] or complex molecules Ni(C≡CR)X(PMe3)3 [R = SiPh3, X = I (14), Br (15); R = Ph, X = I (19), Br (20)]. Dissociation of trimethylphosphane gives square planar trans-Ni(C≡CR)X-(PMe3)2 [R = CMe3, X = Br (4), Cl (5); R = SiEt3, X = Br (8), Cl (9); R = SiiPr3, X = Br (12), Cl (13); R = SiPh3, X = I (16), Br (17), Cl (18); R = Ph, X = I (23), Br (24), Cl (25)] but with R = SiR'3, X = I the title reaction dominates with formation of trans-Ni[C(C≡CR)=CR(C≡CR)]I(PMe3)2 [R = CMe3 (26), SiEt3 (29), SiiPr3 (32)]. Thermal activation is necessary in order to obtain trans-Ni[C≡CR)=CR(C≡CR)]X(PMe3)2 [R = CMe3, X = Br (27), Cl (28); R = SiEt3, X = Br (30), Cl (31); R = SiiPr3, X = Br (33), Cl (34)], while only thermal decomposition is observed with trans-Ni(C≡CR)X(PMe3)2 (R = Ph, SiPh3). Examples for both types of reactivity including structural data are given: trans-Ni(C≡CRSiMe3)Br(PMe3)2 and 25 crystallize in the space group P1. Pentacoordinate 19 (space group P21) adopts a trigonal pipyramid of ligand donor atoms with equatorial phenylethynyl and iodo ligands.
    Zusätzliches Material: 5 Ill.
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  • 241
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    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A-105 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 242
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1811-1813 
    ISSN: 0009-2940
    Schlagwort(e): Vinylferrocene ; Palladium-catalyzed couplin ; (Ferrocenylvinyl)arenes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: (Ferrocenylvinyl)arenes 3, 5, and 7 are obtained from vinylferrocene (1) and substituted aromatic and heteroaromatic halides by palladium-catalyzed Heck-type reactions. Up to three ferrocene units are introduced in one step by the multi-fold reaction of 1,2-dibromo- (4) or 1,3,5-tribromobenzene (6) with 1. The first crystal structure of a bis(ferrocenylvinyl)benzene chromophore (5) is reported.
    Zusätzliches Material: 1 Ill.
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  • 243
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1851-1856 
    ISSN: 0009-2940
    Schlagwort(e): Grignard reagents, 1,3-di- ; Titanocene ; Zirconocene ; Platinum, complexes of ; Rhodium, complexes of ; Iridium, complexes of ; Metallacycles ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Five 1,8-naphthalenediyl transition metal compounds 2 were prepared by treating either 1,8-naphthalenediylmagnesium (1) or 1,8-dilithionaphthalene with the appropriate transition metal dichloride LnMCl2: LnM = Cp2Ti (2a), (PEt3)2Pt (2b), Cp* PPh3Rh (2c), Cp* PPh3Ir (2d), or Cp*2Zr (2e). The resulting metallacycles were characterized by NMR and mass spectrometry. X-ray crystal structure analyses were performed for (1,8-naphthalenediyl)titanocene (2a) and (1,8-naphthalenediyl)bis(triethylphosphane)platinum (2b). Despite the strain induced by the four-membered metal-containing rings, the naphthalene units show remarkably small distortions.
    Zusätzliches Material: 2 Ill.
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  • 244
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1871-1875 
    ISSN: 0009-2940
    Schlagwort(e): Oxidation by HOF ; Hypofluorous acid ; Addition compounds of HOF and HF with acetonitrile ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Oxidation Reactions with HOF and Adducts of HOF and HF with AcetonitrileIn acetonitrile solution HOF oxides CF3SSCF3 via CF3S(O)nSCF3 (n = 1, 2) to yield [CF3S(O)2]2O. Analogously, CF3Se(O)OH and CF3SeX (X = Cl, Br) are oxidized via CF3Se(VI) intermediates to provide finally [CF3Se(O)2]2O. With CH3CN at low temperatures HOF and HF form 1:1 adducts, whose structures have been elucidated by low-temperature X-ray structure analysis. Additional proof for the formation of CH3CN · HF in the liquid phase is provided.
    Zusätzliches Material: 3 Ill.
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  • 245
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1901-1908 
    ISSN: 0009-2940
    Schlagwort(e): Diborane(4) dianion, 1,2-bis(dimethylamino)-1,2-di-9-fluorenyl- ; Li, Na, K, Cs salts ; Ca, Ba salts ; Main group metallocenes ; Hetero-ansa-bridged metallocenes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 1,2-Bis(dimethylamino)-1,2-di-9-fluorenyldiborane(4) (1) is doubly metallated with group 1 and 2 metals to yield metal 1,2-bis(dimethylamino)-1,2-di-9-fluorenyldiborate(4) 2-Li to 2-Ba. The conformations of these compounds in solution are investigated by NMR spectroscopy, and the solid-state structures of 2-Li · 5 THF, 2-K · 4 THF, 2-K · 2 DME, and 2-Ca · 2 THF are determined by X-ray diffraction. All four structures can be described as main group metallocenes. The potassium derivatives form contact ion pairs, leading to polymeric chain-like structures. In contrast, 2-Li · 5 THF exhibits the rare combination of a contact ion pair with a solventseparated ion pair, giving the monomeric structure [Li(THF)4][(fl2B2(NMe2)2)Li · THF]. 2-Ca · 2 THF, which is also monomeric, adapts a severely distorted geometry.
    Zusätzliches Material: 5 Ill.
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  • 246
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 2369-2372 
    ISSN: 0009-2940
    Schlagwort(e): Cyclopentadienyl complexes ; Carbene complexes ; Samarium(II) compounds ; Ytterbium(II) compounds ; Lanthanides, organo- ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Organometallic Compounds of the Lanthanides, 91[1]. - Carbene Complexes of Divalent Samarium and Ytterbium(Imidazol-2-ylidene)lanthanide adducts (C5Me4Et)2Sm-CN-(iPr)CMe=CMeN(iPr) (5b), (C5Me5)2Yb-CN(Me)CMe=CMeN(Me) (6a), (C5Me5)2Yb-CN(iPr)CMe=CMeN(iPr) (6b), and (C5H3tBu2)2Yb-CN(Me)CMe=CMeN(Me) (7a) are obtained from 1,3,4,5-tetramethyl-imidazol-2-ylidene (4a) or 1,4-diisopropyl-2,3-dimethylimidazol-2-ylidene (4b) and (C5Me4Et)2Sm(THF) (1), (C5Me5)2Yb(THF) (2), or (C5H3-tBu2)2Yb(THF) (3). The molecular structure of the ytterbium carbene complex 7a has been determined by X-ray diffraction.
    Zusätzliches Material: 1 Ill.
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  • 247
    ISSN: 0009-2940
    Schlagwort(e): Dinuclear palladium(II) complexes ; Bis(1-methylimidazol-2-yl) ketone ; Pyridine-2-thione ; Pyrimidine-2-thione ; 4-Imidazoline-2-thione, 1-methyl- ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Three novel dinuclear palladium(II) complexes with the chelating ligand bis(1-methylimidazol-2-yl) ketone (bmik) as well as pyridine-2-thiolate (pyt), pyrimidine-2-thiolate (pymt), and 1-methylimidazole-2-thiolate (meimt) as bridging secondary ligands were prepared by reactions of diaqua[bis(1-methylimidazol-2-yl) ketone]palladium(II) nitrate with the ligands in aqueous solution. The thiolates bridge the two metal atoms in the μ-N,S mode. The structures of the following compounds were analyzed by single crystal X-ray diffraction: Bis(μ-pyridine-2-thiolato-N,S)-bis{[bis(1-methyl-imidazol-2-yl) ketone]palladium(II)}nitrate [Pd2(bmik)2-(pyt)2](NO3)2 · 5 H2O (1), bis(μ-pyrimidine-2-thiolato-N1,S)- bis{[bis(1-methylimidazol-2-yl) ketone]palladium(II)} nitrate [Pd2(bmik)2(pymt)2](NO3)2 · 5 H2O (2), and bis(μ-1-methyl-imidazole-2-thiolato-N3,S)-bis{[bis(1-methylimidazol-2-yl) ketone]palladium(II)} nitrate [Pd2(bmik)2(meimt)2](NO3)2 · 4.5 H2O (3). In the cases of 1 and 3 the bridging thiolate ligands show head-to-head orientation. For complex 2 a head-to-tail orientation of the pyrimidine-2-thiolates was found. The metal-metal distances vary from 2.963 Å in complex 3 and 2.915 Å in 1 to the shortest of 2.886 Á in 2. In addition to the X-ray crystallography the three compounds were characterized by 1H-NMR and IR spectroscopy.
    Zusätzliches Material: 6 Ill.
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  • 248
    ISSN: 0009-2940
    Schlagwort(e): Boranes ; Aminoboranes ; Phosphanyliminoboranes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Contributions to the Chemistry of Boron, 221[1].  -  Kinetic and Thermodynamic Product Control in the Addition of HX Compounds to an Amino Phosphanylimino Borane R2N—B≡N—PR2′The reaction of equimolar amounts of HI with tmp=B≡N—PtBu2 (3) (tmp = 2,2,6,6-tetramethylpiperidino group) in an unpolar solvent yields the phosphonium salt [tmp-B=N—PHtBu2]I (4). No such well-defined reaction was observed with triflic or tetrafluoroboric acid. In contrast, HCl reacts with 3 to produce a mixture of tmp-B(Cl)-NH-PtBu2 (5) and tmp - B(Cl) - N=PHtBu2 (6). On heating or on standing at ambient temperature the unique proton of 5 migrates from the N to the P atom with formation of 6, which, therefore, is thermodynamically more stable than 5.
    Zusätzliches Material: 2 Ill.
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  • 249
    ISSN: 0009-2940
    Schlagwort(e): (Trifluoromethyl)sulfane- and -disulfanesulfonic acids ; Mercury compounds ; (Trifluoromethyl)sulfanyl-disulfanyl-, and -sulfinylimine ; Arsenic compounds ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Synthesis and Properties of S-(Trifluoromethyl)polysulfanemonosulfonates CF3SxSO2M [x=1, M = OH, NH4O, 1/2 HgO2, (CH3)2N, NH2; x=2, M = NH4O]*Hydrolysis of CF3SNSO with 2 equiv. of H2O provides [NH4][CF3SSO3] (1), which on treatment with chlorine gives CF3SCl and [NH4][ClSO3]. Trifluoromethyl thiosulfates are synthesized from Hg(SCF3)2 and ClSO2M [M = NH4O, (CH3)3SiO (2), (CH3)2N (3), NH2 (4)]. Insertion of SO3 into Hg(SCF3)2 provides Hg[CF3SSO2O]2 (6). Similarly, S-(trifluoromethyl)thiosulfuric acid (5) is obtained from CF3SH and SO3. New preparations for CF3SXNSO (x=1, 2) are described. These compounds are formed either from Hg(NSO)2 or (CH3)3SiNSO and CF3SxCl in good yields. CF3SSNSO (8) reacts with water to give [NH4][CF3SSSO3] (9). A 1:1 adduct (10) is obtained from CF3SNSO and AsF5. A preliminary X-ray structure investigation proved that AsF5 is coordinated to the oxygen atom. Some reactions of [NH4][CF3SSO3] and CF3SSO2OSi(CH3)3 are mentioned.
    Zusätzliches Material: 1 Ill.
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  • 250
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 501-506 
    ISSN: 0009-2940
    Schlagwort(e): Tripod ligand synthesis ; Tripod iron trisacetonitrile complexes ; Tripod cobalt acetate complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Functionalized Tripod Ligands: Synthesis and Coordination of 1,1,1-Tris[(diphenylphosphanyl)methyl]methaneThe tripod ligand HC(CH2PPh2)3 (4) is easily available from the reaction of 1,3-dichloro-2-(chloromethyl)propane (3) with lithium diphenylphosphide. The ligand 4 itself and two of its coordination compounds, [(HC(CH2PPh2)3)Co(OOCMe)]+-[BPh4]- (5 · BPh4) and [(HC(CH2PPH2)3)Co(OOCMe)]2+ · 2[BF4]- [7 · (BF4)2] have been characterized by X-ray analyses. Coordination of 4 leads to an opening of the CH2—CH—CH2 bond angles (114° in 7 · (BF4)2 and 5 · BPh4 versus 111° in 4). This change in structure is reflected by the unusual low field shift of the methine hydrogen of 7 · (BF4)2 (δ = 3.90) in comparison with the corresponding signal of the free ligand 4 (δ = 1.53).
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 251
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 11-14 
    ISSN: 0009-2940
    Schlagwort(e): Niobium iodide telluride ; Polytellurides ; Chain compounds, one-dimensional ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The new ternary compound Nb4Te17I4 has been prepared and structurally characterized. It crystallizes in the monoclinic system, space group C2/c with unit-cell parameters a = 16.199(4), b = 8.128(2), c = 27.355(6) Å, β = 110.84(2)°, Z = 4. The structure consists of infinite one-dimensional niobium/tellurium chains running parallel to the crystallographic c direction. The chains are separated by iodine atoms. Short and long metal-metal distances alternate in the sequence of three consecutive short bonds ([d ≈ 3.1 - 3.2 Å) and one long (d = 4.268 Å) metal-metal separation. Each Nb atom is eight-coordinate. The composition of the chain is ∞11[(Nb5+)2(Nb4+)2(Te22-)4(Te32-)3(I-)4].
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 252
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 15-21 
    ISSN: 0009-2940
    Schlagwort(e): Copper niobium telluride ; Layer compounds ; Low-dimensional compounds ; Electrical properties ; Band structures ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Synthesis, Structure and Electronic Properties of Cu0.69NbTe2Cu0.69NbTe2 is obtained from the elements in a sealed quartz ampoule at 850°C. The structure of Cu0.69NbTe2 is related to the CdI2 type. The Cu atoms are disordered and situated in tetrahedral sites between the NbTe2 layers. The Nb atoms form zig-zag chains extending in one direction within the layers. This deformation of the Nb sublattice from trigonal symmetry is typical for CdI2 derivatives with formal electron counts close to d2 on the early transition metal. The magnetic susceptibility is temperature-independent between 4 K and 300 K (Pauli paramagnetism). Resistivity measurements confirm the metallic behavior of the compound. The crystal structure and the physical properties are in agreement with the results of tight-binding band-structure calculations.
    Zusätzliches Material: 7 Ill.
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  • 253
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 55-65 
    ISSN: 0009-2940
    Schlagwort(e): Organosilicon p-phenylenediamine derivatives ; Wurster's blue ; PE spectroscopy ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Structures of Sterically Overcrowded and Charge-Perturbed Molecules, 38[1].  -  The Different Conformations of N-Trimethylsilyl-Substituted p-Phenylenediamine Derivatives: Investigation of Single Crystals and in the Gas PhaseThe ESR-proven generation of a Wurster's Blue radical anion by one-electron reduction of N,N,N′,N′-tetrakis(trimethylsilyl)-p-phenylenediamine is rationalized by a posterior singlecrystal structure determination of the neutral molecule, which demonstrates inter alia that the bulky [(H3C)3Si]2N substituents are twisted out of the benzene plane by 83°. In contrast, the skeleton of the sterically congested N,N′-bis(trimethylsilyl)-p-phenylenediamine remains almost planar and, accordingly, allows nN/π interaction between the p-type nitrogen electron pairs of the also flattened [(H3C)3Si]HN groups and the benzene π system. These conformational differences are reflected in the gas-phase photoelectron spectra, in which nN/π ionisation bands are split by less than 1 eV or more than 3 eV, respectively. The evidence for analogous structures of the two organosilicon p-phenylenediamine derivatives in solution is confirmed by geometry-optimized AM1 calculations, which readily explain the surprising insertion of an extra electron into an already electron-rich molecule.
    Zusätzliches Material: 5 Ill.
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  • 254
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 97-99 
    ISSN: 0009-2940
    Schlagwort(e): (Sulfinylthio)phthalimides ; Thiosulfinato complexes ; Platinum complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The oxidative addition of N-[(alkyl- and arylsulfinyl)thio]-phthalimides 3a-d to Pt(PPh3)2(C2H4) gives the platinum(II) thiosulfinato complexes cis-Pt[(S-S(O)-R)(Nphth)(PPh3)2] 4a-d; the structure of N-[(benzylsulfinyl)thio]phthalimide (3c) has been characterized by X-ray crystallography.
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  • 255
    ISSN: 0009-2940
    Schlagwort(e): Host-guest complexes ; Molecular-dynamics (MD) simulation ; Enantioselective gas chromatography ; Cyclodextrins ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The energies of complexation of methyl (R)/(S)-2-chloropropionate [(R)/(S)-2] with heptakis(3-O-acetyl-2,6-di-O-pentyl)-β-cyclodextrin (1) and the structures of the corresponding complexes were determined by molecular-dynamcis (MD) simulations at 300 and 333 K. The geometry of the complexes, the conformations of complexed and uncomplexed 1 and (R)/(S)-2 and the closest H-H distances between host and guest in the complexes were determined from the trajectories. The results correspond to the experimental findings from enantioselective gas chromatography.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 256
    ISSN: 0009-2940
    Schlagwort(e): Triquinacenes ; Indenoindenes ; syn Elimination ; thermal ; Conformational effects ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis of tribenzotriquinacene 4 by a stepwise cyclization strategy involving phenyl-substituted diindan intermediates is discussed in detail. Based on the determination of the anti (α) stereochemistry of the previously known phenyldiindanone 8 by standard electron impact mass spectrometry as well as on synthetical evidence (8 → 12 → 14), the conversion of 8 to the syn (β) phenyl-substituted isomer 20 by means of dehydrogenation-rehydrogenation sequences has been achieved. In particular, the preparation of the isomeric diindenones 15 and 16 as key synthetic intermediates by thermal syn elimination of the corresponding phenylsulfinyl and phenylseleninyl ketones 22 and 25 is described and contrasted to a bromination/dehydrobromination approach adopted from a previous report. The synthesis is completed by reduction of 20 to diindanol 27 followed by cyclodehydration, giving 4 in 14-19% overall yield from 8. Non-cyclizing dehydration of 27 and the isomeric diindanol 9 gives the Δ4b,9-diindene 30 as the most stable non-cyclized isomer of 4. The steric effect of the syn- or anti-oriented phenyl substituents on the preferred conformation of the diindan skeleton is deduced from the contrasting vicinal 1H-1H spin coupling observed for the stereoisomers, e.g. the 9-phenyldiindans 28 and 29.
    Zusätzliches Material: 2 Ill.
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  • 257
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 201-204 
    ISSN: 0009-2940
    Schlagwort(e): Diazo compounds ; Homologation ; Valence isomerization ; Germanium compounds ; Tetrahedranes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Small Rings, 80[1].  -  Tri-tert-butyl(trimethylgermyl)cyclobutadiene and Tri-tert-butyl(trimethylgermyl)tetrahedraneIn the course of our research on silyl-substituted diazo compounds as precursors of cyclobutadienes and tetrahedranes the synthesis of the title compounds 16 and 17 has also been accomplished. Their properties are comparable to those of the silyl-substituted homologous compounds. Tri-tert-butyl(trimethylgermyl)tetrahedrane (17) melts without decomposition at 143°C and thus proves to be as stable as tri-tert-butyl(trimethylsilyl)tetrahedrane. The interconversion of the rectangular forms of tri-tert-butyl(trimethylgermyl)cyclobutadiene (16) proceeds with an activation energy below 4 kcal/mol, which is nearly the same as of tri-tert-butyl(trimethylsilyl)cyclobutadiene.
    Zusätzliches Material: 1 Tab.
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  • 258
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 219-221 
    ISSN: 0009-2940
    Schlagwort(e): Alkenes ; hyperstable ; Hydrogenation ; catalytic ; Hydrocarbons ; concave ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: (1α,6α,7α,8α,12α,17α,18α,19α)-Heptacyclo[17.3.1.18,12.05,23.06,18.07,17.016,24]tetracosa-5(23),16(24)-diene, a Hyperstable AlkeneHydrogenation of the cis-photodimer 1 of acenaphthylene yields the title compound 2, which, though still containing two double bonds, undergoes no further hydrogenation or reaction with bromine for steric reasons. The cyclobutane ring of 2 shows strong steric distortions as revealed by X-ray analysis as well as by force-field and semiempirical MO calculations.
    Zusätzliches Material: 1 Ill.
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  • 259
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 261-265 
    ISSN: 0009-2940
    Schlagwort(e): Bond activation ; C—H ; C—C ; Iron chemistry ; Reaction mechanisms ; Chelate effects ; Tandem mass spectrometry ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: For three α,ω-diphenylalkanes the mechanistic details of the Fe+-mediated activation of C—H and C—C bonds in the gas phase have been elucidated by isotopic labelling experiments. The unimolecular reactions, i.e. dehydrogenation of the alkane chain, formation of ethylene from internal methylene groups, and generation of toluene, proceed largely with high selectivity. Particularly interesting are the results for the dehydrogenation of the Fe+ complex 3-Fe+ of 1,8-diphenyloctane which involves to 93% the internal methylene groups C-4/C-5. In addition, the study of the stereoisotopomers 3c-d provides evidence for the operation of isotopically sensitive branching (“metabolic switching”) in the reaction, and the analysis of the data suggests that the selectivity of the reaction is, most likely, due to a sandwich-type structure.
    Zusätzliches Material: 3 Tab.
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  • 260
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 271-274 
    ISSN: 0009-2940
    Schlagwort(e): Pig liver esterase ; Enantioselective hydrolysis ; Asymmetrized neopentane ; Reactive chiral building block ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A Novel Chiral Building Block with Neopentane Framework for Synthesis: Chemo-Enzymatic Preparation of (R)-CH3C(CH2OSO2CF3)(CH2Cl)(CH2Br)The pig liver esterase (PLE) catalysed hydrolysis of the prochiral malonic ester (BzlOCH2)(Me)C(COOMe)2 (1) leads to its chiral monoester 2 in selectivities up to 81% ee. Compound 2 is an ideal entry point for the enantioselective synthesis of 1,1′,1″-substituted neopentanes CH3C(CH2X)-(CH2Y)(CH2Z) with three different leaving groups, X, Y, and Z. CH3C(CH2OSO2CF3)(CH2Br)(CH2Cl) (8) is a versatile reactive building block for the asymmetric synthesis of compounds containing the neopentane-C5 skeleton.
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  • 261
    ISSN: 0009-2940
    Schlagwort(e): Heterobimetallic complexes ; Iron complexes ; Platinum complexes ; Silyl complexes ; Phosphido bridges ; Hydrido complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Transition Metal Silyl Complexes, 48[1]. - Synthesis of the New Heterobimetallic Dinuclear Silyl Complexes (OC)3(R3Si)-Fe(μ-PR′R″)Pt(1,5-COD)(Fe-Pt), Phosphane Exchange Reactions of (OC)3(R3Si)Fe(μ-PR′R″)Pt(PPh3)2(Fe-Pt), and Preparation of the Dihydrido complexes [(OC)3Fe(μ-PPh2)(μ-H)2Pt(PR3)2][BF4](Fe-Pt)The dinuclear, silyl-substituted complexes (OC)3(R3Si)Fe(μ-PR′r″)Pt(1,5-COD) (1) [μ-PR′R″ = PPh2, PCY2, PHPh; SiR3 = SiPh3, Si(OMe)3] were prepared in high yields by the oxidative addition of the hydrido complexes (OC)3(PHR′R″)Fe(H)-SiR3 to Pt(1,5-COD)2. Upon reaction of (OC)3(R3Si)Fe(μ-PR′R″)Pt(PPh3)2 [μ-PR′R″ = PPh2, PHCy; SiR3 = SiPh3, SiPh2Me, SiPhMeCl, Si(OMe)3] with two equivalents of PR‴3 (PMe3, PBu3, PEt3) or with one equivalent of chelating di-phosphanes (vdpp, dppe, dppm) both PPh3 ligands are displaced, and (OC)3(R3Si)Fe(μ-PR′R″)Pt(PR‴3)2 or (OC)3(R3Si)-Fe(μ-PR′R″)Pt[(PPh2)2X] (X = C=CH2, C2H4, CH2) are formed, respectively. When one equivalent of PMe3 is used, only the PPh3 ligand trans to the μ-PPh2 bridge is substituted, and (OC)3(Ph3Si)Fe(μ-PPh2)Pt(PPh3)(PMe3 is formed. The 1,5-COD ligand in 1 is displaced by P(OR)3 to give (OC)3-(Ph3Si)Fe(μ-PPh2)Pt[P(OR)3]2 (R = Me, Ph). The complexes (OC)3(Ph3Si)Fe(μ-PPh2)Pt(PMe3)2and (OC)3(Ph3Si)Fe(μ-PPh2)Pt[(PPh2)2C=CH2] were characterized by X-ray structure analysis. The short Fe-Si distances [233.0(2) and 235.6(3) pm] and the infrared v(CO) absorptions indicate that the Fe-Pt bonds are quite polar. Protonation of (OC)3(Me2-PhSi)Fe(μPPh2)Pt(PPh3)2 with CF3COOH gives the hydrido-bridged complex [(OC)3(Me2PhSi)Fe(μ-PPh2)(μ-H)Pt-(PPh3)2][O2CCF3]. Upon addition of an excess of HBF4 · Et2O to (OC)3(R3Si)Fe(μ-PPh2)Pt(PPh3)2 (R = Ph, OMe), (OC)3-Si)Fe(μ-PPh2)Pt[Pt[P(OMe)3]2 or (OC)3(Ph2MeSi)Fe(μ-PPh2)-Pt(dppe) R3SiF is split, and the corresponding μ-dihydrido complexes [(OC)3Fe(μ-PPh2)(μ-H)2Pt(PR3)2][BF4] are obtained.
    Zusätzliches Material: 2 Ill.
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  • 262
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 343-346 
    ISSN: 0009-2940
    Schlagwort(e): Azole-borane adducts ; Azaboles ; Imidazabole ; X-ray analysis ; NMR, multinuclear ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Elimination of H2 from the imidazole - borane adduct 1 leads to a mixture of the imidazaboles 2 and 2′. The symmetrical isomer 2 (two H2BNC fragments) is isolated in pure state and characterized by an X-ray structure analysis (monoclinic, space group P21). 2-(Trimethylstannyl)thiazole (3a) and 1-methyl-5-(trimethylstannyl)-1,2,4-triazole (3b) react with triethylborane to form adducts 4 from which, in the presence of an excess of Et3B, tetraalkyltin is elimated to give the thiazabole 5a and the triazabole 5b, respectively. Multinuclear 1H-, 11B-, 13C-, 14N-, and 119Sn-NMR spectroscopy serve for following the reactions (compounds 3 to 5) and to characterize all final products.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 263
    ISSN: 0009-2940
    Schlagwort(e): Tin cations ; triorgano ; Coordination ; s̰ and π ; 1,1-Organoboration ; 1-Alkynyltin compounds ; functionally substituted ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Di-1-alkynyltin compounds 1 of the type Me2Sn(C≡CUL)2 [LU = 2-pyridyl (a), Me2NCH2 (b), MeOCH2 (c), MeOCH=CH (d), EtSCH2 (e)] were prepared and the 1,1-organoboration of 1 with triethyl- (2a) and triisopropylborane (2b) has been studied. The first detectable intermediates were in all cases zwitterionic compounds 3 (from Et3B) and 4 (from iPr3B) with a cationic triorganotin fragment, stabilized by coordinative s̰ L—Sn bonds and by side-on coordination to the C≡C bond of an alkynylborate moiety. The nature of this stabilization has been established by three X-ray analyses (3b, 4b, and 4d) in the solid state and by multinuclear NMR (1H-, 11B-, 13C-, 15N-, 119Sn NMR) in solution. The comparison of the molecular structure of 3b, 4b, and 4d with that of intermediates without functional groups shows that the distance of the tin atom to the C≡C bond is elongated. However, the planar arrangement of all relevant atoms proves that the side-on coordination of the tin atom to the C≡C bond is still present. These intermediates 3 and 4 rearrange to stannoles 5, 6 and/or to 1-stanna-4-bora-2,5-cyclohexadienes 9, 10. In the case of 3b and 3e, 119Sn NMR indicates that dialkenyltin compounds 7b and 7e are also formed as minor products. In the case of 3e, the 3-stannolene 8e is one of the final products. In the stannoles 5 and 6 a coordinative L—B bond is evident, and there is NMR spectroscopic evidence of a weak coordinative L - Sn bond.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 264
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 393-400 
    ISSN: 0009-2940
    Schlagwort(e): Cyclovoltammetry ; Charge-transfer complexes ; HOMO energy ; Naphthols ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Measurement of the Donor Strength of Substituted 1-NaphtholsThe oxidation potential of various substituted naphthols is available by cyclovoltammetry. The donor strength of substituents on the oxidation potential may be explained on the base of substituent increments. When correlating the oxidation potential with the transition energy of charge transfer complexes with TCNE, 1-naphthols with 8-alkoxy substituents and naphthols without oxygen in position 8 are giving different correlation curves. The experimental values correlate well with semiempirically calculated HOMO energies. Our measurements allow to predict the oxidation potentials of hitherto unknown substituted 1-naphthols with high probality. Thus, it may be possible to synthesize 1-naphthols with a defined oxidation potential.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 265
    ISSN: 0009-2940
    Schlagwort(e): Fenestranes ; Polyquinanes ; Centropolyindans ; Polycyclic compounds ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The synthesis and spectroscopic characterization of several benzoanellated [5.5.5]-, [5.5.5.6]-, and [5.5.5.5]fenestranes, including the parent difuso-centrotriindan 7, the parent tetrafuso-centrotetraindan 8 (“fenestrindan”) as well as the tribenzo[5.5.5.6]- and tribenzo[5.5.5.5]fenestranes 27 and 35, are described and discussed in full experimental detail. The highly efficient twofold cyclodehydration of 2,2-dibenzyl-1,3-indandiol 15 and the related spiro-condensed 1,3-indandiols 23 and 29 is the keystep of the synthetic strategy. The new synthetic variant involving the one-pot cyclodehydration/deketalization of the dispiro-ketal diol 29 is particularly convenient. In the case of 7, an alternative Lewis acid-catalyzed double cyclization has been developed. Stereochemical aspects of the 1,3-indandiols and the key tribenzo[5.5.5.6]fenestranes 24 and 25 are discussed in detail.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 266
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 437-444 
    ISSN: 0009-2940
    Schlagwort(e): Reductive coupling ; Oligo(9,10-anthrylene)s, derivatization of, cyclization of ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A homologous series of oligo(9,10-anthrylene)s up to the heptamer have been synthesized by reductive coupling of quinones with lithioanthrylenes, followed by reductive aromatization of the intermediate hydroxy species. The method used allows the introduction of different alkyl substituents, which ensure sufficient solubility of the newly synthesized anthrylene systems in common organic solvents. The solid-state conformations of trimers 4 and 5 have been established by X-ray structure analysis; UV/Vis-spectroscopic investigations in solution reveal the anthracene moieties in 9,10-anthrylenes to exist as electronically independent electrophores. The trianthrylenes can be subjected to electrophilic substitution which regioselectively provides e.g. 10-bromo- and 10,10″-dibromo derivatives. These bromides can easily be converted into the corresponding cyano compounds. Under the influence of potassium hydroxide in quinoline the trimer 5 partially cyclizes to helianthrene compounds.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 267
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A19 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 268
    ISSN: 0009-2940
    Schlagwort(e): Copper(II) complexes, dinuclear ; Schiff bases, macrocyclic ; Redox properties ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Complexes with Macrocyclic Ligands, I. - Dinuclear Copper(II) Complexes with a Totally π-Conjugated Macrocycle of Schiff Base Type: Syntheses, Structures, Electro-, and Magnetochemical PropertiesThe dinuclear copper(II) complexes 6, 7, and 8 of three novel macrocyclic ligands were synthesized by the Schiff base condensation of 2 equiv. of 1,2-phenylenediamine and 2,6-diformylphenol in the presence of 2 equiv. of copper(II) perchlorate and were characterized by X-ray structure analyses, electrochemical investigations (DCV), and variable-temperature magnetic susceptibility measurements. Complex 6 exists in two different solvated crystalline forms. The Copper(II) ions in all three complexes are octahedrally coordinated with long axial distances to solvent molecules or perchlorate ions. The copper ions in 6 (in solvate a) are only five-coordinate and square-pyramidal. The CuIICuII complexes were reduced in successive, quasi-reversible, one-electron steps. The antiferromagnetic exchange interactions were determined. Upon dissolution in acetonitrile complex 8 decomposed to form [Cu(MeCN)4]+ClO-4 and the benzimidazolium percholorate 9 (X-ray structure determination).
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 269
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 489-500 
    ISSN: 0009-2940
    Schlagwort(e): Alkenes ; Nickel complexes ; Stannenes ; Metal-metal bonds ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: {Bis[bis(trimethylsilyl)methyl]stannio(II)}bis(η2-ethene)nickel(0) and Related Compounds, Part IIThe coordinatively unsaturated (16e) (ethene)nickel(0) stannylene complex (C2H4)2Ni=Sn{CH(SiMe3)2}2 (1) reacts with 1,6-heptadiene with preservation of the Ni=Sn bond to yield quantitatively the 1,6-diene derivative (η2,η2-C7H12)Ni=Sn-{CH(SiMe3)2}2 (2). The alkene ligands of both 1 and 2 are readily displaceable. Compounds 1 and 2 react with butadiene at -50°C by a 4-e oxidation of the metal-metal pair Ni(0)/Sn(II) to Ni(II)/Sn(IV) and concomitant reduction of two butadiene molecules to butenediyl moieties to afford stereo-selectively the 16-e complex Ni-cis-{η3(Ni),η1(Sn)-anti-C3H4CH2}2Sn{CH(SiMe3)2}2 (3). Similarly, the reaction of 1 or 2 with isoprene yields regio- and stereoselectively the derivative Ni-cis-{η3(Ni,η1(Sn)-anti-C3(3-Me)H3CH2}2Sn{CH-(SiMe3)2}2 (4). These reactions imply the cleavage of one formal Ni—Sn bond and the formation of two new Sn—C bonds. Upon reaction of 3 with PMe3 the configuration of the allyl system changes and, again fully stereoselectively, the 18-e addition compound (Me3P)Ni-cis-{η3(Ni),η1(Sn)-syn-C3H4-CH2}2Sn{CH(SiMe3)2}2 (5) is formed. When 5 is treated with BPh3, the phosphane ligand is trapped and, kinetically controlled, Ni-cis-{η3(Ni),η1(Sn)-syn-C3H4CH2}2Sn{CH(SiMe3)2}2 (6) is obtained as a stereoisomer of 3. At 40°C 6 slowly rearranges into the thermodynamically stable stereoisomer Ni-trans-{η3(Ni),η1(Sn)-syn-C3H4CH2}2Sn{CH(SiMe3)2}2 (7). Mild protolysis of 3 with pyridine hydrochloride or hydrobromide affords region and stereoselectively (Me3Si)2CH}2(X)SnNi-(η3-1-MeC3H4)(NC5H5) (X = C1, 8a; Br, 8b). In the course of this protonation reaction one butadiene molecule is eliminated, accompanied by a 2-e reduction of the metal-metal pair Ni(II)/Sn(IV) to Ni(II)/Sn(II) and, at the expense of two Sn—C bonds, reformation of a Ni—Sn bond. All compounds are isolated in high yield and fully characterized by 1H-, 13C-, and 31P-NMR spectroscopy.
    Zusätzliches Material: 3 Tab.
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  • 270
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 533-539 
    ISSN: 0009-2940
    Schlagwort(e): Bissulfenyl chlorides ; fluoro substituted ; 1,3-Dithioles ; 1,3,2-Dithiazoles ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Halogen-Carbon-Sulfur Compounds: Syntheses with 1,1,1,4,4,4-Hexafluoro-2-butene-2,3-bissulfenyl ChlorideThe bifunctional bissulfenyl chloride 3 is obtained by chlorination of the dithiete 1 or tetrathiocine 2. By excessive chlorination the saturated bissulfenyl chloride 4 is formed. 3 reacts with primary amines to yield the 1,3,2-dithiazoles 5a-e, whereas by reactions with active methylene compounds like ketones or β-dicarbonyls the compounds 7-14 are obtained with HCl elimination. 13 as well as 14 are converted into the carboxylic acid 15 from which the 1,3-dithiole 17 is obtained by decarboxylation. 3 reacts with disulfene to form tetrakis-(trifluoromethyl)tetrathiafulvalene as well as 4,4′,5,5′-tetrakis(trifluoromethyl)-2,2′-spirobi[1,3-dithiole] (18), whose crystal structure has been determined.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 271
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 557-563 
    ISSN: 0009-2940
    Schlagwort(e): Hydrogen transfer ; Molecule-induced radical formation ; Reduction of C—F bond ; 1-Adamantylfluorodiphenylmethane ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 1-Adamantylfluorodiphenylmethane (2) was reduced to 1-adamantyldiphenylmethane (3) when heated with 9,10-dihydroanthracene to 330°C. From the second-order kinetics, the activation parameters (ΔH
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 272
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994) 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 273
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 611-613 
    ISSN: 0009-2940
    Schlagwort(e): 2,3-Diboratetralin,2,3-bis(dimethylamino)- ; 2,3-Diboranaphthalenediide,2,3-bis(dimethylamino)- ; 2,5-Benzodiborocine,2,5-bis(dimethylamino)-3,4-diethyl-1,2,5,6-tetrahydro- ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Synthesis, Deprotonation, and Ring Expansion of a 2,3-DiboratetralinHerrn Prof. Dr. Helmut Werner zum 60. Geburtstag gewidmet.Reaction of K2[1,2-C6H4(CH2)2] with [Cl(Me2N)B]2 leads to 2,3-bis(dimethylamino)-2,3-diboratetralin (4a) in 58% yield. Deprotonation of 4a with lithium 2,2,6,6-tetramethylpiperi-dide yields the crystalline dilithium salt 6a. Insertion of 3-hexyne into the B—B bond of 4a results in the formation of 2,5-bis(dimethylamino)-3,4-diethyl-1,2,5,6-tetrahydro-2,5-benzodiborocine (7a) in 38% yield. The constitutions of 4a, 6a, and 7a were derived from 1H-, 11B-, 13C-NMR, and MS data and proven for 6a and 7a by X-ray,structure analyses.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 274
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 631-637 
    ISSN: 0009-2940
    Schlagwort(e): N-Isocyanodialkylamines ; N-Isocyanide metal complexes ; Homoleptic complexes ; Stabilization by coordination ; N—N Bond cleavage ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Metal Complexes of Functional Isocyanides, XXIII[1]. - N-Isocyanodialkylamine Complexes of Boron, Rhodium, Palladium, Platinum, and CopperThe N-isocyanodialkylamines CNNEt2, CNNiPr2, and CNNCH(Me)(CH2)3CHMe (1a-c) react with triphenylboron, various transition metal halides, and mono- and dinuclear chloro complexes by addition, substitution, bridge cleavage and reduction to give the complexes Ph3BCNNR2 (2b, c), [MX2(CNNR2)2] (M = Pd, Pt; X = Cl, Br, I) (3-7), [M(Cl)-(CNNR2)(PPh3)2]BF4 (8, 9), cis- and trans-[PtCl2(CNNR2)-(PR′3)] (R′ = Et, Ph) (10-12), [Rh(CNNR2)4]Cll (15b, c) and [Cu(CNNR2)4]ClO4 (16b, c). The complexes [PdX2(CN—NR2)(PPh3)] (X = Cl, Br) (13c, 14c) have been obtained by substitution of an N-isocyanide ligand in 3c and 4c, respectively, with PPh3. The structural assignments are made on the basis of IR, NMR (1H, 13C, 31P, 15N) and mass spectrometry as well as of an X-ray structure analysis of [PdI2(CNNiPr2)2] (5b).
    Zusätzliches Material: 1 Ill.
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  • 275
    ISSN: 0009-2940
    Schlagwort(e): Ethaneselenol, pentafluoro-, IR, Raman, NMR, electron diffraction ; ab initio Calculation ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Reactive E=C(p-p)π Systems, XXXVII[1]. - Pentafluoroethaneselenol: Synthesis, Spectra, and Gas-Phase StructureHerrn Professor Wolfgang Sawodny zum 60. Geburtstag gewidmet.Pentafluoroethaneselenol HSeC2F5 (1) and its deuterated analogue DSeC2F5 (2) are obtained in moderate yields by cleavage of the diselane (SeC2F5)2 with Me3SnH and Me3SnD, respectively. Complete characterization of the labile compounds was accomplished by spectroscopic investigations (IR, Raman, MS; 1H, 13C, 19F, 77Se NMR). The molecular structure was determined by electron diffraction in the gas phase together with ab initio calculations.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 276
    ISSN: 0009-2940
    Schlagwort(e): Organoiron compounds ; Iron catalysts ; Ketone synthesis ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Alkyliron and Alkylcobalt Reagents, IX[1].  -  Rearrangement of Aliphatic Terminal Epoxides to Methyl Ketones by Iron Alkyl Reagents instead of Co2(CO)8 or Noble Metal CatalystsThe highly selective rearrangement of aliphatic terminal epoxides to methyl ketones, hitherto possible only with Co2(CO)8 or noble metal catalysts, occurs smoothly with Me4-FeLi2, Me3FeLi, or the catalytic systems [RLi + 2.5 mol% FeCl3] (R = Me, Bu). This was demonstrated by the rearrangement of 1-decene oxide (1) to 2-decanone (2) (yield 80-81%; Table 1) and 6-bromo-1-hexene oxide (5) to 6-bromo-2-hexanone (6) (yield 78%, Me4FeLi2 applied only). The competition reaction of Me4FeLi2 with 1 and 2-octanone (8) (mole ratio 0.5:1:1) led to 87% 2-methyl-2-octanol (9) and not to the rearrangement 1 → 2. This indicates that Me4FeLi2 - in contrast to the opposite behavior of organo cuprates - reacts faster with ketones than with the aliphatic terminal epoxides. By treatment of 1 with methyl derivatives of MnII, CoII, and NiII or with Bu4FeLi2 (Table 2) other products (3, 4) besides 2 were formed. The rearrangement of 1 with Me4FeLi2 is assumed to start with an oxidative addition and yields 2 as its Li or Fe enolate (trapped with acetanhydride to give 64% of 20) after reductive elimination of CH4. The catalytic rearrangement of 1 with [MeLi + 0.25 mol% FeCl3] very probably occurs in an analogous manner with an super-ate complex Me4FeLi2(MeLi)n as the active species and the Li enolate of 2 as end product (Scheme 4). The aromatic terminal epoxides styrene oxide and α-methylstyrene oxide give various products in the reaction with Me4FeLi2 or Me3FeLi, including the deoxygenation products styrene and α-methylstyrene. These products are exclusively formed on treatment of the epoxides with Me4MnLi2. (Prepared, hitherto in the literature not described compounds: 7 and 10-15.)
    Zusätzliches Material: 3 Tab.
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  • 277
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 691-696 
    ISSN: 0009-2940
    Schlagwort(e): Molecule-induced radical formation, kinetics of ; Catalysis ; ESR spectroscopy ; Radical clock ; Isokinetic relationship ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Bimolecular Formation of Radicals by H-Transfer, 7[1].  -  Bimolecular Formation of Radicals via H-Transfer with Catalysis by 7H-Benz[de]anthraceneThe transfer hydrogenation of α-methylstyrene (2) by 9,10-dihydroanthracene (1) (DHA) with 7H-benz[de]anthracene (8) as a catalyst proceeds already at 210-260°C. Isotopic labeling, ESR spectroscopy, radical clock experiments, solvents effects, and thermochemical calculations support the postulated stepwise radical mechanism induced by bimolecular formation of radicals.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 278
    ISSN: 0009-2940
    Schlagwort(e): [2-(Acylamino)ethenyl]carbene complexes ; Aminocarbene complexes of chromium and tungsten ; Ketene imines, 2-(acylamino)ethenyl ; Pyrroles, synthesis by ring-closing metathesis ; 1,4-Diaminonaphthalenes, synthesis by electrocyclization ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Organic Syntheses via Transition Metal Complexes, 69[1].  -  2-(Acylamino)ethenyl Ketene Imines from [2-(Acylamino)ethenyl]carbene Complexes and their Ring-Closing Metathesis to Pyrroles or Electrocyclization to 1,4-DiaminonaphthalenesHerrn Prof. Helmut Werner zum 60. Geburtstag gewidmet.[2-(Acylamino)ethenyl]carbene complexes LnM = C(OEt) —CH=CPh—[N(COR)Ph] 5 [LnM = (CO)5Cr, (CO)5W; R = C6H5, pMeOC6H4, pNO2C6H4, OtBu] are obtained by N-acylation of [2-(amino)ethenyl]carbene complexes LnM=C (OEt)-CH=CPh(NHPh) (Z)-3 in 72-90% chemical yields with high stereoselectivity. The reaction of (Z) - or (E)-5 with two equivalents of isocyanides RNC 6 (R = cC6H11, tBu) at 20°C gives the isocyanide complexes LnM(RNC) 9 and the [2-(acylamino)ethenyl]ketene imines RN=C=C(OEt)—CH = CPh[N(COR)Ph] 8 (〉95% yields) with configurational retention at the C=C(N) bond. Thermolysis of (Z)-8 (20-80°C) provides an efficient route to pyrroles 11 (90-95%) by a ring-closing metathesis with elimination of isocyanates 10, while the thermolysis of (E)-8, e.g. (E)-8g, at 20°C leads to the formation of 1,4-diaminonaphthalenes, e.g. 12g (〉95% yield), by an electrocyclic ring closure.
    Zusätzliches Material: 1 Ill.
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  • 279
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    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 759-765 
    ISSN: 0009-2940
    Schlagwort(e): Chirality ; Circular dichroism ; Conformational mobility ; Cyclophanes ; [n]Phanes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Deformed Chiral [n]MetacyclophanesThe new dithiametacyclophane 3c and the thiaazametacyclophanes 6a, b are chiral, but do not contain chirality centres. They are obtained by cyclization of 1,3-propanedithiol (2), or of the thiaza precursors 5a, b, with the bis(bromomethyl) compounds 1, 4a, b. The dynamic behaviour of the aliphatic chains in 3c, and 6a, b (flipping/rotation) have been studied by dynamic NMR. X-ray analyses of 3c and 6a document the out-of-plane deformation of the boat-shaped benzene ring. The circular dichroism of enantiomer-enriched 3c is reported.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 280
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 783-785 
    ISSN: 0009-2940
    Schlagwort(e): Tellurides, organo ; Substitution, aromatic ; Tellurium-copper couple ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The Te-Cu couple generated in situ by the reaction of disodium telluride with copper(I) iodide in dry N-methyl-2-pyrrolidone has been found to be a convenient telluration reagent for some activated iodoarenes 1. Using this reagent system, we have prepared by a one-pot synthesis in satisfactory yields several bis(nitroaryl) tellurides 4, which are otherwise laborious to obtain.
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
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  • 281
    ISSN: 0009-2940
    Schlagwort(e): [2-(Amino)ethenyl]carbene complexes ; 3-Amino-1,2-propadienylidene complexes ; (2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine, carbene complexes of ; Ketene imines ; Isocyanides ; Pyrroles ; Alkynylcarbene complexes of chromium and tungsten ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Organic Syntheses via Transition Metal Complexes, 70[1].  -  [2-(Galactopyranosylamino)ethenyl]carbene and 3-(Galactopyranosylamino)-1,2-propadienylidene Complexes on 3-Addition of 2,3,4,6-Tetra-O-pivaloyl-β-D-galactopyranosylamine to Alkynylcarbene Complexes (M = Cr, W).  -  Atropisomeric Galactopyranosyl Pyrroles by Reaction of [2-(Galactopyranosyl-amino)ethenyl]carbene Complexes with IsocyanidesEnantiomeric pure (2-aminoethenyl)carbene complexes LnM=C(OEt)—CH=C(Ph)NHR* (Z)-3 and 3-amino-1,2-propadienylidene complexes LnM=C=C=C(Ph)NHR* 4 [R* = 2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl] are obtained by the addition of galactopyranosylamine R*-NH2 2 to the corresponding alkynylcarbene complexes LnM=C(OEt)—C≡CPh 1 [LnM = (CO)5Cr, (CO)5W]. Treatment of (Z)-3 with two equivalents of tert-butyl isocyanide (5) affords isocyanide complexes 6 and ketene imines 7. The latter cyclize spontaneously to give galactopyranosylpyrroles 8 which form stable atropisomers 8A and 8B.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
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  • 282
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 743-757 
    ISSN: 0009-2940
    Schlagwort(e): Bond formation ; C—C / Host-Guest complexation ; Metacyclophanes ; Conformation, syn, anti ; Hagihara coupling ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Molecular Tweezers from Cyclophane Building BlocksMolecular tweezer compounds 1-6 with convergent carboxyl groups are prepared from suitable functionalized [2.2]-and dithia[3.3]metacyclophane building blocks by using several multistep strategies. The C—C coupling of two cyclophanes according to the Hagihara method leads to alkynespacered double cyclophanes. These new preorganized, acyclic host compounds of the cyclophane-type react as molecular tweezers and can selectively “grasp” guest molecules and bind them strongly. X-ray analyses underline the syn conformations of the dithia[3.3]- and the anti conformation of the [2.2]metacyclophanes.
    Zusätzliches Material: 10 Ill.
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  • 283
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. A41 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 284
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 797-804 
    ISSN: 0009-2940
    Schlagwort(e): Heteronuclear complexes ; Ligand [(en)2MIII(OH)2]+ (M = Cr, Co) ; Complexes of third group elements ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Complexes of Third Group Elements with [(en)2MIII(OH)2] Ligands (M = Cr, Co)Heteronuclear complexes are formed on reaction of cis-[(en)2-MIII(OH)(H2O)]2+ (M = Cr, Co; en = ethylenediamine) with A1III, GaIII, InIII, and T1III in aqueous solution. The following salts with tetranuclear cations have been isolated: [A1{(OH)2-Cr(en)2}3](S2O6)3 · 13 H2O (1), [A1{(OH)2Co(en)2}3](S2O6)3 · 5 H2O (2), [Ga{(OH)2Co(en)2}3](S2O6)3 · 5 H2O (3), [In{(OH)2-Cr(en)2}3](S2O6)3 · 6 H2O (5), and [In{(OH)2Co(en)2}3]-(ClO4)4Cl2 · 4 H2O (6). Furthermore, the dinuclear neutral complexes [InCl4{(OH)2Cr(en)2}] (4) and [TlCl4{(OH)2-Cr(en)2}] · 0.5 H2O (7) are prepared. X-ray analyses confirm that in all cases the [(en)2MIII(OH)2] groups act as bidentate ligands in the hydroxo-bridged heterometallic complexes.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 285
    ISSN: 0009-2940
    Schlagwort(e): Chromium tricarbonyl(η6-1,3,5-triphenyl-2,4,6-trimesityl-1,3,5,2,4,6-triphosphatrnane)- ; 1,3,5,2,4,6-Triphosphatriborinane ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The preparation of tricarbonyl(η6-1,3,5-triphenyl-2,4,6-trimesityl-1,3,5,2,4,6-triphosphatriane)chromium (4) is reported. Its X-ray structure reveals an orientation of the Cr(CO)3 moiety with respect to the almost planar B3P3 ring typical of an arene metal tricarbonyl complex.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 286
    ISSN: 0009-2940
    Schlagwort(e): Lithium compounds ; Hydrazines ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Dilithium N,N′-Bis(trimethylsilyl)hydrazide and a Hydrolysis Product: Side-On- and End-On-Coordinated Li Cations to N2-2 and O2-2N,N′-Bis(trimethylsilyl)hydrazine is converted into the dilithium derivative [(Me3Si)2N2Li2] · 2 thf (1) by nBuLi. Compound 1 forms a tetramer which lies on a crystallographic inversion centre. The Li+ ions are found to be end-on to the N—N units and also coordinated by thf, but three Li+ ions are also positioned symmetrically above the N—N bonds. The hydrolysis of 1 in air leads to the formation of [(Me3SiOLi)4 · Li2O2 · LiN(SiMe3)2] · 2 thf (2) which contains four oxide and one peroxide ions. The O2-2 unit is side-on-coordinated by three Li+.
    Zusätzliches Material: 2 Ill.
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  • 287
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    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 887-892 
    ISSN: 0009-2940
    Schlagwort(e): Configuration, absolute ; Alkanols, chiral ; Acetals ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Chiral Lactols, XI. - A Method for the Determination of the Absolute Configuration of Chiral AlkanolsChiral secondary alcohols which are protected with the enantiomerically pure lactol 1 or 2 show significant differences in 13C-chemical shifts around the glycosidic linkage. An easy method for determination of the absolute configuration of secondary alcohols based on this fact is described.
    Zusätzliches Material: 3 Tab.
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  • 288
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 897-903 
    ISSN: 0009-2940
    Schlagwort(e): Dendrimers ; Supramolecular chemistry ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Dendrimers and Dendrimer Building Blocks with Trisubstituted Benzene and “Hexacyclene” as Core UnitsThe preparation of new dendritic compounds containing 1,3,5-substituted aromatic units or “hexacyclene” is described. Bulky dendrimers are obtained in few generations starting with polyfunctional core units like 1, 4, 5, 12, and hexacyclene (21). The dendrimers were synthesized by using both the divergent method (for 7) and the convergent method (for 13 and 22). 22 is the first dendrimer containing a crown unit as core.
    Materialart: Digitale Medien
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  • 289
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    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 941-946 
    ISSN: 0009-2940
    Schlagwort(e): Epoxidation ; Benzofuran ; Benzofuran epoxide ; Quinone methide ; Benzofuran-2-one ; 2,4-Cyclohexadien-1-one, spiroepoxide ; cis-Ene dione ; Perester, β-hydroxy- ; 1,3-Benzodioxole ; Keto enol ester ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The oxidation of the benzofurans 1a-f (tetrahydrobenzofurans 1g, h) with excess m-CPBA is reported. The in situ generated, highly reactive benzofuran epoxides 2a-f and their quinone methides 3a-f (cis-ene diones 3g, h) afford the labile tautomeric peroxy esters 5 and 5′ by nucleophilic addition of the peroxy acid. On elimination of m-chlorobenzoic acid, the peroxy esters 5/5′ of the benzofuran derivatives 1a-f rearrange thermally to the keto esters 6 by C—C cleavage or to the spiro epoxides 7 by C—O cleavage. The latter undergo thermal isomerization to the 1,3-benzodioxoles 8 and Diels-Alder cycloaddition to the corresponding dimers 9. Independently, the keto esters 6 and the 1,3-dioxoles 8 were synthesized by thermolysis of the dioxetanes 11. The tautomeric m-CPBA adducts 5/5′ of the persistent ene diones 3g, h, derived from the tetrahydrobenzofuran derivatives 1g, h, rearrange as well to the spiro epoxides 7g, h. In contrast to the benzofuran derivatives 6a-f, the keto enol ester 6h suffers Baeyer-Villiger rearrangement with another molecule of m-CPBA to form the ene diester 10h.
    Zusätzliches Material: 1 Tab.
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  • 290
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    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 921-932 
    ISSN: 0009-2940
    Schlagwort(e): Bicyclo[3.3.0]octane, derivatives of ; Semibullvalene ; Tricyclo[3.3.0.02-8]octa-3,6-diene ; Cyclooctatetraenes, substituted ; Cyanohydrins, O-(trimethylsilyl)- ; Hydrogen fluoride  -  phosphorus oxychloride  -  pyridine, elimination of trimethylsilanol by ; Phenyl cuprate reagent, conjugate addition of ; Phase-transfer catalysis ; Chlorination by hexachloroethane  -  sodium hydroxide ; Cyclization by dehydrochlorination ; Endoperoxides by triplet oxygen ; 2 H-Pyran, derivative of ; Thermochromism ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Addition of trimethylsilyl cyanide to the diphenylbicyclo[3.3.0]octanedione 8c is catalyzed by the potassium cyanide/18-crown-6 complex and produces a mixture of the diastereomeric bis[O-(trimethylsilyl)cyanohydrins] endo- and exo-10c (3:2). The hydrogen fluoride - pyridine complex in phosphorus oxychloride as solvent and, subsequently, an excess of pyridine convert the mixture of diastereomers 10c into the unsaturated y,y′-diphenyldinitrile 11. This is converted into the red semibullvalene 4 in a single step by treatment with hexachloroethane and concentrated aqueous sodium hydroxide in the presence of tetrabutylammonium hydroxide as phase-transfer catalyst  -  Above 30°C, 4 isomerizes in solution to a mixture of the cyclooctatetraenes 12 and 13. While the red crystals of 4 are stable in the atmosphere, in the dark affording the endoperoxide 16 and the yellow 2H-pyran derivative 17 (7:1) which result from parallel reactions. Only at temperatures as high s 110°C, 16 slowly rearranges to 17 which reacts further to yield well-defined but still unknown products. The simultaneous formation of 16 and 17 at low temperatures is interpreted in terms of endo and exo attack, respectively, of triplet oxygen at the benzylic carbon atoms of the semibullvalene 4 or the isomeric bicyclic diradical 21.  -  The structures of the new compounds are based on spectroscopic evidence and X-ray diffraction analyses of 4, endo-10c, 11, 16, and 17. The semibullvalene 4 exists as a pair of rapidly rearranging degenerate valence tautomers in solution and in the crystal as well. In the solid state, 4 exhibits apparent C2 symmetry and equal atomic distances C2-C8 and C4-C6 (201.9 pm). Because true degeneracy is highly unlikely in the crystal, the equal distribution of two non-equivalent valence tautomers at room termperature results from a fortuitous cancelling of the ΔH° and TΔS° terms governing the equilibrium.  -  The red colour of 4 in the crystal and in solution is due to a maximum at 444 nm which disappears on cooling. Thus, 4 not only belongs to the family of thermochromic semibullvalenes and barbaralanes devoid of a long wavelength chromophor like 1, 6 and 14, but also shows the most intensive maximum at the longest wavelength observed so far.
    Zusätzliches Material: 7 Ill.
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  • 291
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    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994) 
    ISSN: 0009-2940
    Schlagwort(e): Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 292
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 985-990 
    ISSN: 0009-2940
    Schlagwort(e): Silyl triflates ; Polysiloxanes ; Polycarbosilanes ; Polysilylenealkynes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Bis(trifluoromethylsulfonyloxy)organosilicon Compounds as Synthetic Materials for New Silicon PolymersThe new polycarbosilanes, polysiloxanes, and polysilylenealkynes 1c-6c were obtained by condensation of electrophilic α,ω-bis(trifluoromethylsulfonyloxy)organosilicon compounds 1b-6b with nucleophiles such as organolithium and organomagnesium compounds. The required silyl triflate derivatives 1b-6b have been prepared by reaction of the corresponding amino-, allyl-, or phenylsilanes 1a-6a with trifluoromethanesulfonic acid.
    Materialart: Digitale Medien
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  • 293
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 991-995 
    ISSN: 0009-2940
    Schlagwort(e): Copper(II) complexes ; Mangan(II) complexes ; trinuclear ; Schiff bases ; macrocyclic ; Redox properties ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Complexes with Macrocyclic Ligands, II.  -  Synthesis, Structure and Electrochemical Properties of a Macrocyclic Cu2IIMnII Complex of Schiff Base TypeA novel trinuclear Cu2Mn complex 4 of a macrocyclic Schiff base ligand obtained by condensation of 5-tert-butyl-2-hydroxy-1,3-benzenedicarbaldehyde with 1,2-phenylenediamine was synthesized. The molecular structure of 4 was determined by X-ray diffraction revealing a sandwich-type structure as depicted by Figure 2. Electrochemical investigations (DCV measurements) showed two one-electron reduction steps for the copper ions at E1/2 = -1.383 and -1.652 V (vs. Cp2Fe/Cp2Fe+).
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 294
    ISSN: 0009-2940
    Schlagwort(e): Ring enlargement reactions ; Spirocyclic cobaltaphosphazene ; Eight-membered carbon-free inorganic rings ; Tetrahedral CoE4 core (E = O, S, Se) ; Phosphazenoid skeleton ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Chemistry of Polyfunctional Molecules, 112.  -  Ring Enlargement Reactions of a Spirocyclic Cobaltaphosphazene with Oxygen, Sulfur, and SeleniumHerrn Prof. Dr. Ekkehard Lindner zum 60. Geburtstag gewidmet.The spirocyclic cobaltaphosphazene 1 which contains cobaltconnected three-, five-, and six-membered rings undergoes ring enlargement reactions by treatment with O2, S8, and Se8. The resulting paramagnetic spirocyclic cobalta-phosphazenoids 2a-c (E = O, S, Se) consist of eight-membered chelate rings connected at the spiro-cobalt(II) centre forming a tetrahedral CoE4 core. The compounds 2a-c have been characterized by X-ray analyses, 1H, 13C(1H), 31P(1H) NMR, IR, Raman, UV/Vis/NIR, EI/FD mass spectroscopy, and magnetic measurements.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 295
    ISSN: 0009-2940
    Schlagwort(e): Selenadiphosphiranes ; Selenatriphosphetanes ; Molecular dynamics ; Phosphacycles ; Selenium compounds ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Pentamethylcyclopentadienyl-Substituted Selenadiphosphirane and Selenatriphosphetane: Synthesis, Structure, Dynamic, and Some ReactionsHerrn Prof. R. Schmutzler zum 60. Geburtstag gewidmet.1,2,3-Tris(pentamethylcyclopentadienyl)cyclotriphosphane (1) reacts with selenium to form the insertion product 2,3,4-tris(pentamethylcyclopentadienyl)selenatriphosphetane (2), which is trapped as the selenium-coordinated pentacarbonylchromium complex 4. Compound 4 is the first isolated selenatriphosphetane complex. Reaction of 2 with selenium yields 2,3-bis(pentamethylcyclopentadienyl)selenadiphosphirane (3). 3 replaces thf of Cr(CO)5thf to give the chromium complex 5. The reaction of 3 with K[Fe(CO)2Cp*] leads to the substitution product 6 and the bicyclic phosphane 7. The X-ray structures of 3 and 4 are presented. The dynamic behavior of 3-6 is discussed.
    Zusätzliches Material: 2 Ill.
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  • 296
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    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1031-1035 
    ISSN: 0009-2940
    Schlagwort(e): Lithium-(fluorosilyl)phosphanides ; Phosphanides, lithium-(fluorosilyl)(phosphanyl)- ; Silylidenephosphanes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Evidence for a Structure-Reactivity Relationship of Crowded Substituted Lithium (Fluorosilyl)phosphanidesThe molecular structures and the reactivity of the new solvated lithium (fluorosilyl)phosphanides 1a, 2a, and 2b has been investigated. The unusual solid state structures of 1a and 2b are established by X-ray crystallography. Whereas the lithium centre in 1a is bound to phosphorus and solvated by three molecules of THF, the electronical saturation of the lithium centre in 2b is achieved by a Li—P bond, tridentate chelatization (fluorine, phosphorus, nitrogen), and the additional coordination of one molecule of THF. The trigonal-planar geometry at phosphorus in 1a is unprecedented for derivatives of this type and reflects the steric demand around the phosphorus and the possibility of πp/σ*sic hyperconjugation. The Si—P bond lengths [P—SiC(Phenyl) 2.186(2) and P—SiF 2.164(2) Å] are significantly shorter than in related pyramidally configurated derivatives (1b, c: P—SiC 2.21, P—SiF 2.18 Å). Both phosphorus atoms in 2b are pyramidally coordinated, but the intramolecular chelate coordination of the lithium centre causes much smaller bonding angles at the Si—P phosphorus atom [sum of bonding angles 238.4(2) (PSi), 312.5(1)° (PN)]. 1a as well as 2a, b show quite different reactivity as compared to 1b-d due to their unusual structures. Heating of solutions of 1a and 2a, b in toluene or hexane does not give the expected stable silylidenephosphanes (Si=P) by elimination of LiF. Instead, rearrangement reactions of the Si=P intermediates 6, 8 lead to the new heterocycles 5, 9. A single-crystal X-ray diffraction analysis of 5 has been performed. The Si2P2 cyclobutane ring is planar, and the NMe2 groups at the ring silicon atoms are cis-orientated.  -  Interestingly, 2b eliminates LiNiPr2 at 20°C in a kinetically controlled process to form the tetraphosphacyclobutane 7 as the major product. Presumably, the diphosphene 8 is an intermediate in this reaction.
    Zusätzliches Material: 3 Ill.
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  • 297
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    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1037-1039 
    ISSN: 0009-2940
    Schlagwort(e): Borolanes ; Boroles, 2,5-dihydro ; 3,7-Diborabicyclo[3.3.0]oct-1(5)-enes ; 2,5-Diborapentalenes, 1,2,3,4,5,6-hexahydro- ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: 3,4-Dimethyleneborolanes and 3,7-Diborabicyclo[3.3.0]oct-1(5)-enesThe tetramethyleneethane derivative K2[C2(CH2)4] which is readily prepared from 2,3-dimethylbutadiene by metallation with the Lochmann-Schlosser base reacts with BC12(NR2) (R=Me, Et, iPr) to give the highly reactive, liquid 1-(dialkylamino)-3,4-dimethyleneborolanes (3). These dienes react with activated magnesium to give soluble magnesium adducts 5 which upon treatment with BC12(NR2) (R = Me, iPr) yield crystalline 3,7-bis(dialkylamino)-3,7-diborabicyclo-[3.3.0]oct-1(5)-enes (4). The crystal structure of the dimethyl-amino compound 4a was determined by X-Ray-diffraction. The molecule of 4a shows crystallographic C2h symmetry with an almost perfectly planar skeleton.
    Materialart: Digitale Medien
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  • 298
    ISSN: 0009-2940
    Schlagwort(e): Osmium(II) complexes ; Alkyl(carbonyl)hydrido complexes ; Allylhydrido complexes ; Fragmentation, metal-initiated ; C—H Activation ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Studies on C—H Activation, X.  -  Synthesis of Alkyl(carbonyl)hydrido- and Allylhydridoosmium Complexes by Metal-initiated Fragmentation of Primary Alcohols and OlefinsHerrn Professor Dr. E. Lindner zum 60. Geburtstag gewidmet.The reaction of [(Mes)OsCl2]n (1) with RCH2OH/NaOH in the presence of propene leads to complete fragmentation of the primary alcohol and formation of the alkyl(carbonyl)hydrido complexes [(Mes)OsH(R)(CO)] (2-7). The corresponding chloro derivatives [(Mes)OsC1(R)(CO)] (8-13) are obtained either by H/C1 exchange from 2-7 and CC14 or on treatment of [(Mes)OsR2(CO)] (16-21) with HC1 at -78°C. The carbonylosmium(II) compound [(Mes)Os(CO)C12] (15) reacts with iC4H9MgI to give a mixture of [(Mes)Os(iC4H9)2(CO)] (21), [(Mes)OsI(iC4H9)(CO)] (22), and [(Mes)Os(CO)I2] (23), whereas the reaction of 15 with C6H11CH2MgBr yields [(Mes)Os(CH2C6H11)2(CO)] (24), the olefin complex [(Mes)Os(CH2=C6H10)(CO)] (25), and [(Mes)OsH(Br)(CO)] (26). The alkylhydridoosmium(II) compound [(Mes)OsH(CH2C6H11)(CO)] (28) is obtained from the chloro derivative 27 and Mg/Hg/C2H5OH. Treatment of 1 with iC3H7OH/NaOH and propene or isobutene affords the η3-allylhydrido complexes [(Mes)OsH(η3-2-RC3H4)] (31, 32) in about 85% yield, while the reaction of 1 with iC3H7OH/NaOH and tert-butylethene gives [(Mes)Os(CH2=CHtC4H9)2] (35). The X-ray structural analysis of [(Mes)OsH(η3-2-CH3C3H4)] (34), which like the corresponding η3-allylchloro compound 33 is formed from the η3-allylhydrido complex 31 or 32 and CC14, reveals a half sandwich-type structure with an exo arrangement of the methallyl ligand.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 299
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 1003-1013 
    ISSN: 0009-2940
    Schlagwort(e): Metallocene complexes, bent ; Titanium complexes ; Vinylidene complexes ; Transition metal complexes ; Heterodinuclear complexes ; Carbene complexes ; Early-Late heterodinuclear complexes ; Metallacycles ; Oxatitanacyclobutane complexes ; Oxatitanacyclopentene complexes ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Cyclic Isomeric Four- and Five-Membered Heterodinculear Carbene Complexes  -  Formed from a Titanocene Vinylidene Fragment and Metal CarbonylsThe four-membered heterodimetallic carbene complexes Cp*2 16 [LnM: Cr(CO)5 (a), Mo(CO)5 (b), W(CO)5 (c), CpRe(CO)2 (f), Mn2(CO)9(g), Re2(CO)9 (h), Fe(CO)4 (i), Rh(acac)(CO) (i)] are easily prepared by trapping the vinylidenetitanocene [Cp*2Ti=C=CH2] fragment 6 with the corresponding metal carbonyls. The vinylidenetitanocene 6 is generated in a favourable manner from Cp*2Ti(CH3)CH=CH2 (13) or Cp * (Fv)TiCH = CH2 (14) [Fv: C5(CH3)4CH2] by a 1,3-H shift (α elimination) at room temperature. The formation of 16 is characterized by a preferred suprafacial [2 + 2] cycloaddition. Starting from Cp*2 (5) or 14 and transition metal carbonyls unexpected isomeric five-membered titanacycles Cp*2 8 [MLn = a-c, MnCp(CO)2 (d), MnCp′(CO)2 (e), f-i] are obtained at higher temperatures (70-100°C). These oxatitanacyclopentenes 8 are formed also upon heating via the kinetic product 16 with high yield, as a result of a 1,2-hydrogen shift, proved for c, g, h. From the spectroscopic data an η1-vinylcarbene structure is deduced, exhibiting a cis- (16) or trans-configurated (8) LnM=C—C=C sequence. An X-ray structure analysis shows the importance of the acyl resonance form in 8a, typically observed for such heterodimetallic carbene complexes. The reversible liberation of the metal carbonyl is a remarkable property of complexes 16 in solution, whereas the thermodynamic product 8 shows the typical properties of Fischer carbene complexes.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 300
    ISSN: 0009-2940
    Schlagwort(e): λ3-Phosphaalkyne, 2-amino- ; PE Spectroscopy ; Calculations, ab initio ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Reactive E=C(p-p)π-Systems, XXXVIII.  -  Molecular and Electronic Structure of 2-(Diisopropylamino)-1λ3-phosphaethyne iPr2NC≡PThe molecular structure of 2-(diisopropylamino)-1λ3-phosphaethyne iPr2NC≡P (3) has been investigated by X-ray diffraction using a single crystal grown from the melt at -50.2°C. Bond distances and angles indicative for the electronic structure are: P°C 155.2(2), N—C(sp) 131.2(3) pm, P—C—N 179.2(2)°; with a sum of angles 359-8° the nitrogen atom has a trigonal-planar coordination. The reported geometrical parameters of 3 have been reproduced by ab initio calculations (3-21G and DZP basis), showing that the lengthening of the P°C and the shortening of the C—N bond can be rationalized by the interaction of the π system of the triple bond with the 2p orbital at N. The He(I) photoelectron spectrum of 3 confirms the strong interaction.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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