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  • Aluminium Hydride complexes  (1)
  • Nickel complexes  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 1267-1273 
    ISSN: 0009-2940
    Keywords: Aluminium Hydride complexes ; Nickel(0) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Lewis Acidity of Nickel(0). XII. - Dimethylaluminium Hydride Complexes of Nickel(O)Ni(CDT) reacts with (1-azabicyclo[2.2.2]octane)dimethylaluminium hydride in pentane to form the yellow crystaline addition compound (C7H13N)(Me2AlH)Ni(CDT) (2c). In its crystal structure 2c exhibits a Ni-H-Al three-center bond. Displacement of the CDT ligand of 2c with ethene in pentane at 0°C yields light brown crystals of (C sb7H13N)(Me2AlH)Ni(C2H4)2 (4), which is also obtained from Ni(C2H4)3 and (C7H13N)-Me2AlH). Complex 4 is converted by CO at - 78°C into the colorless carbonyl complex (C7H13N)(Me2AlH)Ni(CO)3 (5). 2c and 4 may be considered as model compounds for intermediates of the nickel(0)-catalyzed hydroalumination reaction of alkenes.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 127 (1994), S. 653-655 
    ISSN: 0009-2940
    Keywords: 1,6-Diynes ; Nickel complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Structure of (R3P)Ni(1,6-Heptadiin) ComplexesDisplacement of the alkene ligand in Ligand-Ni(0)(1,6-diene) complexes by 1,6-heptadiyne, the parent 1,6-diyne, affords the complexes (Me3P)Ni(η2,η2-C7H8) (1) and (Ph3P)Ni(η2,η2-C7H8) (2). According to an X-ray structure analysis of the PMe3 derivative 1 the nickel atom is ideally trigonal-planar coordinated by the phosphane and both C≡C bonds. The increased stability of the complexes as compared to Ligand-Ni(HC≡CH)2 complexes is referred to the strong chelating effect which is special to the 1,6-functionalization. The compounds can be considered to be model complexes for the key intermediates of numerous transition metal-mediated coupling reactions of (substituted and unsubstituted) 1,6-diynes.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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