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  • 1,6-Dienes  (1)
  • 1-[1,7-Dicarba-closo-dodecaboran(12)-1-yl]aldoses  (1)
  • 1990-1994  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 2667-2675 
    ISSN: 0009-2940
    Keywords: Alkene ligands ; 1,6-Dienes ; Nickel complex ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,6-Heptadiene Nickel(0) Complexes:rac/meso-(μ-η2,η2-C7{Ni(η 2,η2-C7H12)}2 und L-Ni(η2,η2-C7H12)Ni(CDT) dissolves in 1,6-heptadiene with displacement of the CDT to yield the dinuclear homoleptic product rac/meso-(μ- η2,η2-C7H12){Ni(η2, η2-C7H12)}2 (1) as a mixture of stereoisomers, in which the nickel atoms are trigonal-planar coordinated by a chelating 1,6-diene ligand and one C=C bond of a bridging diene ligand. The stereoisomers differ in the coordination mode of the bridging diene ligand.-The bridging diene ligand in 1 can be displaced by various donor/acceptor molecules. In pentane, 1 reacts with ethene to yield a solution of mononuclear (C2H4)Ni(η2,η2-C7H12) (2). With alkynes unstable complexes are formed of which the anticipated ethyne derivative (C2H2)Ni(η2,η2-C7H12) (3) decomposes explosively at - 100°C. With isocyanides, methylenephosphoranes, methyllithium, amines, pyridines, phosphanes, and phosphites (i.e. C, N, P donors) crystalline complexes of type L-Ni(η2.η2 C7H12) have been obtained, of which the derivatives with L=tBuN = C 4, Me3PCH2 5, LiCH3 6, C7H13N7, C5H5N 8, Me3P 9, iPr3P 10, Ph3P 11, (PhO)3P 12 are characterized here. For 11 the crystal structure has been determined.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1993 (1993), S. 831-835 
    ISSN: 0170-2041
    Keywords: Boron neutron capture therapy ; 1-[1,7-Dicarba-closo-dodecaboran(12)-1-yl]aldoses ; 1-[m-Carboran-1-yl]aldoses ; Boranes ; Carbohydrates ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monolithiated 1,7-dicarba-closo-dodecaborane(12) reacts with O-isopropylidene derivatives of D-erythrono-1,4-lactone (1), L-mannono-1,4-lactone (3) and with tetra-O-trimethylsilylated D-glucono-1,5-lactone (2) and D-gulono-1,4-lactone (4) to give the title compounds after deprotection. An X-ray structure analysis of the protected L-mannofuranose carborane derivative 9 reveals that the more stable anomer has the β-L configuration.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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