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Monomer sequence control via living anionic copolymerization : synthesis of alternating, statistical, and telechelic copolymers and sequence analysis by MALDI ToF mass spectrometry.

机译:通过活性阴离子共聚进行单体序列控制:交替,统计和远螯共聚物的合成,并通过MALDI ToF质谱进行序列分析。

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摘要

Diphenylethylene (DPE) is a monomer which has attracted significant interest from both academia and industry. DPE can undergo (co)polymerization by living anionic polymerization but is incapable of forming a homopolymer due to steric hindrance. Herein the copolymerization of DPE and 1,1-bis(4-tert-butyldimethylsiloxyphenyl)ethylene (DPE-OSi) with styrene or butadiene is described in order to produce (functional) copolymers with controlled comonomer sequences—either alternating or telechelic. The copolymer sequences are inherently controlled by relative reactivity ratios, which in turn can be tuned by both monomer structure and the polarity of the polymerization solvent. The compositions of the copolymers prepared in this study were analyzed by 1H NMR spectroscopy and MALDI ToF mass spectrometry, the latter offering a unique opportunity to demonstrate perfect alternating sequences and insight into other sequences such as telechelic polymers.ud
机译:二苯乙烯(DPE)是一种单体,引起了学术界和工业界的极大兴趣。 DPE可以通过活性阴离子聚合进行(共)聚合,但是由于空间位阻而不能形成均聚物。本文描述了DPE和1,1-双(4-叔丁基二甲基甲硅烷氧基苯基)乙烯(DPE-OSi)与苯乙烯或丁二烯的共聚反应,以生产具有受控共聚单体序列(交替或远螯)的(官能)共聚物。共聚物序列固有地由相对反应率控制,该相对反应率又可以通过单体结构和聚合溶剂的极性进行调节。通过1H NMR光谱和MALDI ToF质谱分析了本研究中制备的共聚物的组成,后者提供了独特的机会来证明完美的交替序列以及深入了解其他序列,例如远螯聚合物。

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