个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:大连理工大学
学位:博士
所在单位:化工学院
学科:应用化学. 精细化工
办公地点:E-330
联系方式:wmren@dlut.edu.cn
电子邮箱:wmren@dlut.edu.cn
Crystalline Stereocomplexed Polycarbonates: Hydrogen-Bond-Driven Interlocked Orderly Assembly of the Opposite Enantiomers
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论文类型:期刊论文
发表时间:2015-02-09
发表刊物:ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
收录刊物:SCIE、EI、PubMed、Scopus
卷号:54
期号:7
页面范围:2241-2244
ISSN号:1433-7851
关键字:carbon dioxide; crystalline; enantiopure polycarbonates; epoxides; polymer stereocomplexes
摘要:Four novel crystalline stereocomplexed polymers are formed by mixing isotactic (R)- and (S)-polycarbonates in 1:1 mass ratio. They show the enhanced thermal stability and new crystalline behavior, significantly distinct from the component enantiomer. Two stereocomplexed CO2-based polycarbonates from meso-3,4-epoxytetrahydrofuran and 4,4-dimethyl-3,5,8-trioxabicyclo[5.1.0]octane have high melting temperatures of up to 300 degrees C, about 30 degrees C higher than the individual enantiomers. Isotactic (R)- or (S)-poly(cyclopentene carbonate) and poly(cis-2,3-butene carbonate) are typical amorphous polymeric materials, however, upon mixing both enantiomers together, a strong interlocked interaction between polymer chains of opposite configuration occurs, affording the crystalline stereocomplexes with melting temperatures of about 200 degrees C and 180 degrees C, respectively. A DFT study suggests that the driving force forming the stereocomplex is the hydrogen-bonding between carbonate units of the opposite enantiomers.