Issue 9, 1992

New ring-opening metathesis polymerization catalyst based on a five-coordinate tungsten(VI) alkylidene complex containing an ortho-chelating arylamine ligand; X-ray structure of [W{C6H4(CH2NMe2)-2}([double bond, length half m-dash]NPh)([double bond, length half m-dash]CHSiMe3)(CH2SiMe3)]

Abstract

At –78°C [W([double bond, length half m-dash]NPh)(CH2SiMe3)3Cl] reacts with 2-[(dimethylamino)methyl]phenyllithium in diethyl ether to produce a tetra-organotungsten(VI) complex which decomposes by an Hα-elimination reaction generating a novel tungsten(VI) alkylidene with intramolecular coordination of an amine function; this complex reacts with norbornene to provide a cis-polymer that is the result of a selective ring-opening metathesis.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 717-719

New ring-opening metathesis polymerization catalyst based on a five-coordinate tungsten(VI) alkylidene complex containing an ortho-chelating arylamine ligand; X-ray structure of [W{C6H4(CH2NMe2)-2}([double bond, length half m-dash]NPh)([double bond, length half m-dash]CHSiMe3)(CH2SiMe3)]

P. A. van der Schaaf, W. J. J. Smeets, A. L. Spek and G. van Koten, J. Chem. Soc., Chem. Commun., 1992, 717 DOI: 10.1039/C39920000717

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