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  • Nickel complex  (1)
  • Nickel complexes  (1)
  • 1
    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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  • 2
    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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