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Stereoselective Copolymerization of Unprotected Polar and Nonpolar Styrenes by an Yttrium Precursor: Control of Polar‐Group Distribution and Mechanism
Author(s) -
Liu Dongtao,
Wang Meiyan,
Wang Zichuan,
Wu Chunji,
Pan Yupeng,
Cui Dongmei
Publication year - 2017
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201611066
Subject(s) - copolymer , monomer , polar , styrene , polymer chemistry , polymerization , methylene , yttrium , chemistry , materials science , polymer , organic chemistry , oxide , physics , astronomy
Styrene underwent unprecedented coordination–insertion copolymerization with naked polar monomers ( ortho ‐/ meta ‐/ para ‐methoxystyrene) in the presence of a pyridyl methylene fluorenyl yttrium catalyst. High activity (1.26×10 6 g mol Y −1 h −1 ) and excellent syndioselectivity were observed, and high‐molecular‐weight copolymers (24.6×10 4 g mol −1 ) were obtained. The insertion rate of the polar monomers could be adjusted in the full range of 0–100 % simply by changing the loading of the polar styrene monomer. Strikingly, the copolymers had tapered, gradient, and even random sequence distributions, depending on the position of the polar methoxy group on the phenyl ring and thus on its mode of coordination to the active metal center, as shown by tracking the polymerization process and DFT calculations.