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- W2950598209 abstract "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." @default.
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- W2950598209 date "2000-03-01" @default.
- W2950598209 modified "2023-10-16" @default.
- W2950598209 title "Methyl(2-phosphanylphenolato[P,O])nickel(II) Complexes – Synthesis, Structure, and Activity as Ethene Oligomerization Catalysts" @default.
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- W2950598209 doi "https://doi.org/10.1002/(sici)1099-0682(200003)2000:3<431::aid-ejic431>3.0.co;2-q" @default.
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