344770-69-0Relevant articles and documents
Novel non-symmetric nickel-diimine complexes for the homopolymerization of ethene: Control of branching by catalyst design
Schmid, Markus,Eberhardt, Robert,Kukral, Jürgen,Rieger, Bernhard
, p. 1141 - 1146 (2007/10/03)
Non-symmetric diimine ligands (Ar-N=C(CH3)-(CH3)C=NAr*; Ar: 2,6-diisopropyl-phenyl; Ar*: 2,6-di(4-tert-butyl-phenyl)phenyl (4b), 2,6-di(4-OCH3)-phenyl)phenyl (4c)) were synthesized and converted in-situ into the corresponding nickel dibromo complexes (5b, c) by reaction with (DME)NiBr2. The complexes were activated for ethene polymerization by treatment with MAO at ambient temperature. The resulting high molecular weight polymer products (Mw > 4.0 × 106 g mol-1) have a branched microstructure (predominantly methyl groups), as indicated by 13C NMR spectroscopy. The degree of branching can be controlled by a proper choice of the 2,6-diphenyl modified aniline moieties resulting in melting transitions ranging from 92 - 130°C.