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  • Inorganic Chemistry  (22)
  • 1995-1999  (20)
  • 1950-1954  (2)
  • 1997  (20)
  • 1954  (2)
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Publisher
Years
  • 1995-1999  (20)
  • 1950-1954  (2)
Year
  • 1
    ISSN: 0009-2940
    Keywords: Silicenium ion ; Iminosilane ; Aluminate ; Silicon ; Aluminium ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Lithiated text-butylaminolfluorosilanes react with aluminum trichloride in ether, eliminating LiF to give AlCl3 adducts of iminosilanes  -  aminosiliceniotrichloroaluminates {R2Si-NCMe3·AlCl3}, which thermally form the dimethylazomethine- aluminium trichloride, Me2C=NH·AlCl3.
    Additional Material: 2 Ill.
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  • 2
    ISSN: 0009-2940
    Keywords: Bis(tetramethylipiperidino)aluminum halides ; Alkoxy((tetramethylpiperidino)aluminum halides ; 27Al-NMR spectra ; Aluminum ; Amides ; Synthetic methods ; Bridging ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-Lithio-2,2,6,6-tetramethylpiperidine [Li(tmp)] reacts with AlX3 (X = Cl, Br) in diethyl ether/ n-hexane solution to generate the products of substitution and ether cleavage, [tmpAl(X)(μ-OEt)], (la, X = Cl; 1b, X = Br). However, when the reaction is allowed to proceed in n-hexane alone, an almost quantitative yield of compounds tmp2AlX (2a, X = Cl; 2b, X = Br; 2c, X = I) is obtained. According to 27AI-NMR spectroscopy, mass spectroscopy, cryoscopy, and X-ray crystal structure determinations, these compounds are monomeric in the solid state, in solution, and in the gas phase. 2b reacts with AgBF4 yielding the fluoride-bridged dimer (tmp2AlF), 2d, as shown by X-ray crystal structure determination.
    Additional Material: 3 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 453-462 
    ISSN: 0009-2940
    Keywords: Cycloadditions ; Catalysis ; 1-Oxa-1,3-dienes ; Molybdenum ; stereoselectivity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Molybdenum-mediated [6 + 2]-cycloaddition reactions of unsaturated ketones to cyclotri- or -tetraenes, e.g. cyclohepta-1,3,5-triene or cyclooctatetraene, proceed under very mild conditions, in high yields and with excellent stereoselectivity starting from the appropriate dicarbonylbis[π4-(1-oxa-1,3-diene)]molybdenum complexes. The stereochemistry of the product arising from the reaction of dicarbonylbis[π4-(5-methylhex-3-en-2-one)]molybdenum with cyclohepta-1,3,5-triene allows one to deduce a stepwise mechanism for this addition. The reactants are fused, as would be expected from an exo-type approach, thus indicating an intermolecular attack of the cycloheptatriene. Tungsten oxadiene complexes are effective in analogous reactions at somewhat reduced reaction rates. Catalytic cycloadditions are observed in several cases when 1-5 mol% of the highly reactive dicarbonylbis[π4-(R-(+)-pinocarvone)]molybdenum is employed as the catalyst. Cycloadducts are formed diastereospecifically in most cases. When cyclooctatrienes are employed as reactants, a sequence of electrocyclization of the triene and subsequent [4 + 2]-cycloadditon occurs with high selectivity and efficiency, leading to a pentacyclic ketone. The product structure reveals an endo-type approach of the polyene in this case.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 241-246 
    ISSN: 0009-2940
    Keywords: (2-Pyrrolidinylmethoxo)borane, anomalous dimer ; 5-Phenyl-3,4-dimethyl-1,3,2-oxazaborolidine, anomalous dimer ; Reaction intermediates ; Boron compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of (S)-prolinol (LH) with H3B · THF proceeds via [L2BH2〈]BH4, which decomposes with elimination of hydrogen at ca. -40°C to give the BH3 adduct of spirocyclic 7. On heating, 7 loses more H2 to give the “anomalous” dimerization product 11, which features a tetracoordinated B atom in a “tetrahedral” BN2O2 unit and another B atom in an N2BH2 environment. It is also shown that the product resulting from the reaction of pseudoephedrin with H3B·THF undergoes an analogous anomalous dimerization, affording product 8.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 1123-1127 
    ISSN: 0009-2940
    Keywords: Vanadium ; Cryptands ; Ionophors ; Phosphatases ; Decavanadate ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Treatment of a C222-vanadyl-AMP complex (C222 = cryptand-222, AMP = adenosine monophosphate) with Me2NH in the presence of air yielded centrosymmetric dihydrogen-decavanadate H2V10O428, sandwiched by two diprotonated C222 molecules. An X-ray crystal-structure analysis was performed of this compound with the overall composition [C222(H+)2]2[H2V10O28] · 2 1/2, H2O. Protonation sites in the anion are μ2-oxygen atoms linking two different vanadium centres. Protonation sites at the cryptand are the nitrogen and/or oxygen atoms of one of the -[CH2]2O[-CH2|2O|CH2]- bridges. The relevance of the compound for the stabilisation and transport of the kinase and phosphatase inhibitor decavanadate by biogenic ionophores is addressed.
    Additional Material: 2 Ill.
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  • 6
    ISSN: 0009-2940
    Keywords: Benzo-1,3,2-diphosphaborolanes ; Benzo-1,3,2-diphosphaborolane dimmers ; Benzo-1,4,2,3-diphosphadiborinanes ; Rearrangement reaction ; Pentacarbonyl chromium complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of benzo- 1,3,3-diphosphaborolanes C6H4(PR)2BR' (R = H, iPr, SiMe3; R' = R2N, R) has been prepared by several routes and characterized by spectroscopic and - in part - by X-ray diffraction methods. They feature pyramidal P atoms with the substituents in antiperiplanar positions. The P atoms act as coordination sites for the (CO)5Cr fragment. In contrast to the R2N-bearing benzo-1,3,2-diphosphaborolanes, the derivative C6H4(PH)2BCMe3 (4f) dimerizes by additional B-P bond formation to produce a pentacyclic system (4f)2. - The reaction of C6H4(PHNa)2 with B2(NMe2)2Cl2 in THF/hexane yields the acyclic phosphanylborane Me2NB(PH-C6H4PH2)2 (15). However, if C6H4[P(iPr)Li]2 is allowed to react with B2(NMe2)2Cl2, the benzo-1,4,2,3-diphosphadiborinane 13 is obtained, together with its rearrangement product 2-bis(dimethylamino)borylbenzo-1,3,2-diphosphaborolane 14 which dimerizes to (14)2.  -  In contrast, the almost planar ring of the 2,3-dimesitylbenzo-1,4,2,3-diphosphadiborinane (16) possesses P and B atoms with a planar geometry. Short B-B and B-P bonds suggest that this new heterocycle can be regarded as a 6π electron system. Moreover, the benzo-1,5,2,3,4-diphosphatriborepane 18 forms readily forms readily from C6H4(PHNa)2 and Br(Me2N)B-B(N-Me2)-B(NMe2) Br to give a tub-shaped seven-membered C2B3P2 ring system with the P atoms in a pyramidal and the B atoms in a planar environment.
    Additional Material: 10 Ill.
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  • 7
    ISSN: 0009-2940
    Keywords: Aggregations ; Complex, tert-butyl methyl ether ; diastereotopomerization, (EIZ) ; NMR, coupling, constants, HH, CH, CLi ; NMR, Lithiation shifts ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Improved preparations of 2,6-dimethylstyrene (5) and its α-bromo derivative (10) are described. The Br/Li exchange reaction of 10 provides single crystals of the title compounds 11 or 12, which were characterized as disolvated dimers by X-ray analyses. A similar dimer persists in diethyl ether, tert-butyl methyl ether, and toluene at all accessible temperatures, with significant lithiation NMR shifts (relative to 5) partially due to charge delocalization from the sp2-carbanionic center. Some NMR coupling constants are typical of the dimeric aggregate. The configurational (E,Z) lability is quantified in toluene solution.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 399-404 
    ISSN: 0009-2940
    Keywords: Disilylamides ; Group 4 Complexes ; Polymerization ; Metallacycles ; Titanium ; Zirconium ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of metallacyclodisiladiazanes has been prepared. Lithiated (SiMe2NHtBu)2 (1) reacts with TiCl4 · 2 THF to give (SiMe2NtBu)2TiCl (4). Methylation or fluorination of 4 leads to (SiMe2NtBu)2TiMe2 (8) and (SiMe2MtBu)2TiF2 (9), respectively. The reaction of ZrCl4 · 2 THF with lithiated 1 or [SiMe2NH(4-FC6J4)]2 (2) yields (SiMe2NtBu)2ZrCl2 (5) and [SiMe2N(4-FC6H4)]ZrCl2 · THF (7), respectively. The lithiated ligand [SiMe2NH(2,6-iPr2C6H3)]2 (3) reacts with noncoordinated ZrCl4 to give [SiMe2N(2,6-iPr2C6H3)]2ZrCl2 (6). X-ray structural analysis of 9 showed it to be a fluorine-bridged dimer in the solid state. Compounds 4, 6, 8 and 9 were found to be catalysts for the polymerization of ethylene.
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  • 9
    ISSN: 0009-2940
    Keywords: Vanadium ; Haloperoxidase ; Schiff bases ; Diethanolamine ; Water ligation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of vanadyl sulfate with the Schiff base H2L1 derived from o-vanillin and glycine leads to [VIVO(H2O)L1 (1), treatment of which with acetyl chloride affords cis-[VIVCl2L1] (2). Reaction of [VO(acac)2] with the Schiff base H2L2 derived from o-hydroxynaphthaldehyde and o-hydroxyaniline under aerobic conditions yields [{VVO(L2)}2μ-O] (3), which undergoes methanolysis in excess methanol to form [VVO(MeOH)(OMe)L2] (5a). Complex 5a is also obtained via [VVOCl(L2)] (4) and MeOH. On treatment of 3 with an equimolar amount of ethanol, [VVOCl(L2)] (4) and MeOH. On treatment of 3 with an equimolar amount of ethanol. [VVO(OEt)L2] (5b) is obtained. With the chiral tertiary bis(ethanol)amine (S)- or (R)-(HOCH2CH2)2NCH(Ph)Me, H2L3, [VO(acac)2] loses only one acetylacetonate (1-) ligand, and the complexes (S)- and (R)-[VVO(acac)L3] (6a) are formed. As is evident for the corresponding reaction with (HOCH2CH2)2NPh, H2L4, which affords [VVO(acac)L4 (6b), the substitution is a second-order process (rate constant 0.013 M-1 h-1). 5a…MeOH, 5b, (R)-6a, and (S)-6a have been structurally characterized by single crystal X-ray diffraction analysis. The molecular connectivities have also been established for 1-H2O. All of the structurally characterized complexes contain an O*O3N donor set (O* denotes a doubly-bonded oxo group) and thus model the coordination environment of the active site in vanadate-dependent haloperoxidases. This model character is particularly pronounced in 5b, the coordination geometry of which is half-way to trigonal-bipyramidal. 5a and 6a contain, in addition to the O*O3N set, a labile V-O or V-N bond, respectively, which may mimic substrate binding to the active centre. 6a is also of relevance to the enantioselective peroxide oxidation of sulfides to sulfoxides by catalyst systems containing vanadium and H2L3.
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  • 10
    ISSN: 0009-2940
    Keywords: Phosphorus ; Arsenic ; Germanium ; Inorganic heterocycles ; Metal amides ; Fluorinated ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of potassium Rf-amide [Rf = tris(trifluoromethyl)phenyl](2) with PCl3, AsC13, and GeC12 · dioxane yield new four-membered inorganic heterocycles [RfNPCl]2 (3), [RfNAsC1]2 (4), and [RfNGe]2 (5), respectively. On the other hand, the reaction of Rf-amide 2 with two equivalents of RfPCl2 leads to the formation of the imino-γ3-phosphane RfN=PRf (6) and the diamino-γ3-phosphane (RfNH)2PRf (7). The iminophosphane 6 reacts with Ni(CO)2(PPh3)2 and forms the complex [Ni(PPh3)2(RfN=PRf)] (9), in which the imino- phosphane coordinates to the metal through the phosphorus lone pair. Treatment of lithium amide 2 with transition metal chlorides ZnCl2 and FeCl2 yields the imido/amido spirocyclic metal derivatives 9 and 10, respectively. Compounds 3-10 have been extensively characterized by their analytical and mass, IR, and NMR (1H, 19F, and 31P) spectroscopy. Further, the molecular structures of all the compounds have been unambiguously determined by single-crystal X-ray diffraction studies. The diazadigermetidine 5 crystallizes in a fluorescent-yellow orthorhombic and a yellow monoclinic crystal modification. The results obtained reveal the role of Rf, group in stabilizing new multiple bonded systems and inorganic heterocycles. A skeletal rearrangment of the Rf ligand is observed in the reactions leading to compounds 9 and 10. Moreover, the preparation of compounds 9 and 10 indicates the limitation of the use of this ligand in the preparation of new metal-amide systems, especially where the metal atoms have a strong tendency for the formation of strong M—F bonds.
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