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两性离子交替聚合制备半结晶且可回收的环状聚硫脲烷

Zwitterionic Alternating Polymerization to Generate Semicrystalline and Recyclable Cyclic Polythiourethanes.

作者信息

Tan Dawei, Hu Xin, Cao Zheng, Luo Ming, Darensbourg Donald J

机构信息

School of Materials Engineering, Changshu Institute of Technology, Changshu, Jiangsu 215500, China.

Jiangsu Key Laboratory of Environmentally Friendly Polymeric Materials, School of Materials Science and Engineering, Jiangsu Collaborative Innovation Center of Photovoltaic Science and Engineering, Changzhou University, Changzhou, Jiangsu 213164, China.

出版信息

ACS Macro Lett. 2020 Jun 16;9(6):866-871. doi: 10.1021/acsmacrolett.0c00302. Epub 2020 May 29.

Abstract

Synthesis of cyclic, semicrystalline, and recyclable polythiourethanes was realized via the catalyst-free zwitterionic alternating copolymerization of -alkyl aziridines with carbonyl sulfide (COS) under mild conditions. The copolymerization proceeded efficiently at room temperature and generated copolymers with fully alternating linkages in more than 99% selectivity in 5 min under solvent-free conditions. Notably, the copolymers are typical semicrystalline thermoplastics with melting temperatures up to 137 °C (-butyl-substituted) or 170 °C (ethyl-substituted). The resulting polythiourethanes are predominantly cyclic as evidenced by H NMR and MALDI-TOF mass spectroscopies. Remarkably, the cyclic copolymers could be recycled into N-substituted cyclic thiourethanes in quantitative yield by heating at 250 °C for 2 h.

摘要

通过在温和条件下使N-烷基氮丙啶与羰基硫(COS)进行无催化剂的两性离子交替共聚,实现了环状、半结晶且可回收的聚硫脲的合成。该共聚反应在室温下高效进行,在无溶剂条件下5分钟内以超过99%的选择性生成具有完全交替键的共聚物。值得注意的是,这些共聚物是典型的半结晶热塑性塑料,其熔点高达137℃(N-丁基取代)或170℃(乙基取代)。1H NMR和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)表明,所得聚硫脲主要为环状。显著的是,通过在250℃加热2小时,环状共聚物可以以定量产率再循环为N-取代的环状硫脲。

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