Syndioselective Coordination (Co)Polymerization of AlkyneSubstituted Styrenes Using Rare-Earth Metal Catalysts
writer：Zhen Zhang, Yanli Dou, Zhongyi Cai, Dongtao Liu, Shihui Li and Dongmei Cui
keywords：Alkyne-Substituted Styrenes, Syndioselective Polymerization
source：期刊
Issue time：2020年
Developing convenient methods to introduce functional groups into syndiotactic polystyrene has gained increasing attention in recent years. Herein, we report the coordination polymerization of 4-(1-hexynyl)styrene (HES), 4-(phenylethynyl)-styrene (PES), and 4-(trimethylsilyl)ethynylstyrene (TES) with half-sandwich scandium precursor C5Me4PhSc(CH2C6H4NMe2-o)2 (1) and constrained-geometry-configuration (CGC) precursors C13H8CH2PySc(CH2SiMe3)2 (2, Py = C5H4N) and 2,7-(tBu)2C13H8CH2PyLn(CH2SiMe3)2(THF)n (Ln = Sc (3a), n = 0; Y (3b), Lu (3c), n = 1). Under mild conditions, perfect syndiotactic products (rrrr > 99%) are produced by homopolymerizations of HES, PES, and TES. The random copolymerizations of TES and styrene (St) proceed smoothly with 3b, and the insertion fractions of TES are tuned in the range of 0?100 mol % via changing the TES-to-St feed ratio. The trimethylsilyl groups are facilely eliminated from the TES-based polymers by tetrabutylammonium fluoride to give terminal ethynyl-containing polystyrenes, the reactions of which with an azide compound, carbon dioxide, and anthracene-9-aldehyde afford a series of functional syndiotactic polystyrenes.