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η3-Benzyl-Nickel-Diimine Complex: Synthesis and Catalytic Properties in Ethylene Polymerization

✍ Scribed by Viviane Fassina; Carolina Ramminger; Marcus Seferin; Raquel S. Mauler; Roberto F. de Souza; Adriano L. Monteiro


Book ID
102493359
Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
73 KB
Volume
24
Category
Article
ISSN
1022-1336

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✦ Synopsis


Abstract

The oxidative addition of benzyl chloride to Ni(cod)~2~ in the presence of 1,4‐bis(2,6‐diisopropylphenyl)acenaphthenediimine followed by chloride abstraction affords [(η^3^‐CH~2~C~6~H~5~)Ni(α‐diimine)][PF~6~] (α‐diimine = 1,4‐bis(2,6‐diisopropylphenyl)acenaphthenediimine) in 70% yield. The complex is active in ethylene polymerization in the presence of methylaluminoxane and under mild reaction conditions. The polyethylenes obtained are highly branched, have very low densities, do not show T~m~ or measurable crystallinity and have molecular weights ranging from 80 × 10^3^ to 290 × 10^3^ g · mol^−1^.

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📜 SIMILAR VOLUMES


Nickel Chelate Complexes of 2-Alkylpheny
✍ Joachim Heinicke; Manuela Koesling; Robert Brüll; Wilhelm Keim; Hans Pritzkow 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 340 KB 👁 2 views

2-Diphenylphosphanyl-and 2-alkylphenylphosphanyl-4-hindered or retarded. The reactivity of 1d remains high towards nickel salts in polar solvents, but in contrast to 1a-c, methylphenols 1 or their silyl ethers 2 and equimolar amounts of nickelocene react in benzene preferably to give yielding 4, a s