Novel Cr-PNP complexes as catalysts for the trimerisation of ethylene.

Cr(III) complexes of tridentate PNP ligands have been prepared and evaluated as catalysts for ethylene trimerisation, with several giving high activity and excellent selectivity towards 1-hexene when activated with methylaluminoxane.

Selective Hydrovinylation of Styrene in a Membrane Reactor: Use of Carbosilane Dendrimers with Hemilabile P,O Ligands.

A codimerization of styrene and ethene can be carried out continuously in a nanofiltration membrane reactor with dendritic Pd complexes such as 1. The selectivity of the reaction is increased considerably under continuous conditions. The activity and selectivity of monomeric model complexes and the dendritic catalysts were compared in batch reactions.

2-phosphanylphenolate nickel catalysts for the polymerization of ethylene.

The previously unknown methallylnickel 2-diorganophosphanylphenolates (R=Ph, cHex) were synthesized and found to catalyze the polymerization of ethylene. To explore the potential for ligand-tuning, a variety of P-alkyl- and P-phenyl-2-phosphanylphenols was synthesized and allowed to react with [Ni(cod)(2)] (cod=1,5-cyclooctadiene) or with NiBr(2).DME and NaH. The complexes formed in situ with [Ni(cod)(2)] are generally active as ethylene polymerization catalysts with all the ligands tested, whereas the latter systems are inactive when 2-dialkylphosphanylphenols are applied. M(w) values, ranging from about 1000 to about 100000 g mol(-1), increase for various R(2)P groups in the order R=Ph

First Cr(III)-SNS complexes and their use as highly efficient catalysts for the trimerization of ethylene to 1-hexene.

Cr(III) complexes of tridentate SNS ligands have been prepared and evaluated as catalysts for ethylene trimerization, with several giving very high activity and excellent selectivity toward 1-hexene when activated with methylaluminoxane. The new complexes illustrate the potential of sulfur-based ligands on early transition metals for catalysis.