Two enantiomers of a chiral binaphthyl-bridged salen dichlorozirconium (IV) complex (namely R-L-1 and S-D-1) were synthesized and tested as pre-catalysts for 4-methyl-1-hexene (4MH) polymerization. Their behavior was compared with that of the same complex in its racemic form. Isotactic poly(4- methyl-1-hexene) was produced in both cases, but the polymerization of racemic 4MH promoted by the optically active catalysts preferentially consumed one antipode, showing some stereoselectivity for the process.

Stereospecific and Stereoselective Polymerization of 4-Methyl-1-hexene by Enantiomeric Binaphthyl-Bridged Salen Dichlorozirconium (IV) Complexes

STRIANESE, MARIA;LAMBERTI, Marina;MAZZEO, Mina;PELLECCHIA, Claudio
2007-01-01

Abstract

Two enantiomers of a chiral binaphthyl-bridged salen dichlorozirconium (IV) complex (namely R-L-1 and S-D-1) were synthesized and tested as pre-catalysts for 4-methyl-1-hexene (4MH) polymerization. Their behavior was compared with that of the same complex in its racemic form. Isotactic poly(4- methyl-1-hexene) was produced in both cases, but the polymerization of racemic 4MH promoted by the optically active catalysts preferentially consumed one antipode, showing some stereoselectivity for the process.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11386/1660231
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