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  • Structure  (2)
  • Alkynylnickel halides  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 621-627 
    ISSN: 1434-1948
    Schlagwort(e): Nickel ; Oxidation ; Phenols ; Structure ; Dynamic NMR spectroscopy ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reaction of substituted phenols and dioxygen with Ni(PMe3)4 yields the low-spin tetracoordinate diphenolatonickel compounds Ni(OAr)2(PMe3)2 [ArOH = 2-tert-butylphenol (1), 2-tert-butyl-4-methylphenol (2), 2-tert-butyl-6-methylphenol (3), 2,4-di(tert-butyl)phenol (4), 2-tert-butyl-4-methoxophenol (5), 2-chloro-4-tert-butylphenol (6), 2-isopropylphenol (7), 3-tert-butylphenol (8)]. As is revealed by variable temperature 1H- and 13C-NMR spectroscopy the complexes constitute a mixture of two isomers, each of which can be observed separately at lower temperatures when interconversion is slower. An additional 6-carbaldehyde function transforms the phenolate into a chelating ligand, giving rise to a high-spin hexacoordinate compound Ni(OAr)2(PMe3)2 (9). X-ray crystal-structure determinations of 2 and 3 show a trans square-planar structure, and that of 9 shows a trans octahedral arrangement of donor atoms P2O4. Bulky substituents in the 3- or 4-position, or non-demanding substituents in the 2-position, are less effective in stabilizing molecular diphenolatonickel complexes.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 2027-2032 
    ISSN: 1434-1948
    Schlagwort(e): Nickel(0) ; Oxidation ; Phenols ; Structure ; Ion pairs ; Hydrogen bonds ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Admission of molecular oxygen to a solution containing Ni(PMe3)4 and substituted phenols (ArOH) affords bisphenolatonickel compounds trans-Ni(OAr)2(PMe3)2 [ArOH = 2-chlorophenol (1), 2-bromophenol (2), 2,4,6-trichlorophenol (3)]. In the absence of dioxygen the phenols reversibly protonate the nickel complex to form ionic compounds [NiH(PMe3)4]+ Y- containing hydrogen-bonded anions Y = [H2(2-Cl-C6H4O)3] (4), [H(2-OH-C6H4COO)2] (5). As a side-reaction, formal insertion of nickel to give 2-hydroxyphenylnickel compounds Ni(Ar′)X(PMe3)3 [Ar′ = 2-OH-C6H4; × = Br (6), I (7)], trans-Ni(Ar′)Cl(PMe3)2 [Ar′ = 2-OH-3,5-Cl2-C6H2 (8)] and trans-Ni(OAr)Cl(PMe3)2 [Ar = 2,4,6-Cl3-C6H2 (9)] is observed. An X-ray crystal structure determination of 1 shows a trans square planar arrangement of donor atoms, that of 6shows a distorted square pyramid, while 4 contains tetrahedral nickel cations with a delocalized hydrogen atom and triphenolate anions H2(ArO)3-.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    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
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