Syndio- and isoselective coordinative chain transfer polymerization of styrene promoted by ansa-lanthanidocene/ dialkylmagnesium systems

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Abstract

Combinations of the discrete neutral allyl ansa-lanthanidocenes {Me 2C(Cp)(Flu)}Nd[1,3- (SiMe3)2C3H 3] and rac-{Me2C(Ind)2}Y[1,3- (SiMe 3)2C3H3] with di(n-butyl)magnesium constitute efficient binary catalytic systems for the stereocontrolled coordinative chain transfer polymerization of styrene, yielding near-perfect syndio- and isospecific polystyrenes, respectively, with high activities and productivities. By adjusting the amount of di(n-butyl)magnesium, up to 200 polymer chains can be generated per lanthabide center, and good control of the molecular weight features enables the tailoring of low to medium molecular weight polymers. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Sarazin, Y., De Frémont, P., Annunziata, L., Duc, M., & Carpentier, J. F. (2011). Syndio- and isoselective coordinative chain transfer polymerization of styrene promoted by ansa-lanthanidocene/ dialkylmagnesium systems. Advanced Synthesis and Catalysis, 353(8), 1367–1374. https://doi.org/10.1002/adsc.201100059

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