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  • Alkynylnickel halides  (1)
  • Homogeneous catalysis  (1)
  • 1
    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.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1434-1948
    Schlagwort(e): Methylnickel complexes ; 2-Phosphanylphenolate ; Chelates ; Homogeneous catalysis ; Oligomerization ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Reactions of various substituted 2-phosphanylphenols 1a-f with half-molar amounts of cis-[MeNi(μ-OMe)(PMe3)]2 have been found to yield square-planar methyl(2-phosphanylphenolato)(trimethylphosphane)nickel(II) complexes 2a-f. 2JPP coupling constants of 305-316 Hz at low temperature indicate a trans-configuration for the products, while broad 31P-NMR signals at room temperature can be attributed to rapid dissociation of PMe3. Reaction with excess 1 gave rigid bis(2-phosphanylphenolato)nickel(II) complexes as exemplified by 3e, whereas addition of PMe3 to 2a led to the pentacoordinate methyl(2-phosphanylphenolato)bis(trimethylphosphane)nickel(II) complex 4a. Higher yields of 4a and 4d were obtained by reactions of 1a and 1d with Me2Ni(PMe3)3. Single-crystal X-ray diffraction analyses of 3e and 4a have revealed the structures as square-planar trans-bis- and trigonal-bipyramidal mono(2-phosphanylphenolato)nickel(II) P1O-chelate complexes, respectively. The methylnickel complexes 2 and 4 have been found to be effective one-component catalysts for the oligomerization of ethene. High conversions (〉 96%) were achieved with the P-basic derivatives 2e, 2f, and 4d bearing one or two branched alkyl groups (isopropyl, tert-butyl), whereas the diphenylphosphanyl derivatives were less active; 4d gave shorter oligomers than 2e or 2f.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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