A designed synthetic strategy toward poly(isosorbide terephthalate) copolymers: a combination of temporary modification, transesterification, cyclization and polycondensation. Issue 42 (11th September 2015)

• Record Type: Journal Article
• Authors: Feng, Long; Zhu, Wenxiang; Zhou, Wen; Li, Chuncheng; Zhang, Dong; Xiao, Yaonan; Zheng, Liuchun
• Is Part Of: Polymer chemistry. Volume 6:Issue 42(2015)
• Page Start: 7470
• Page End: 7479
• Publication Date: 2015-09-11
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c5py01167a
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : After a combination of temporary modification, transesterification, cyclization and polycondensation, a series of high- M n and high- T g poly(isosorbide terephthalate) copolymers were synthesized. Abstract : A designed synthetic strategy to overcome the low reactivity of isosorbide (Is) and terephthalic acid (TPA) is developed for the preparation of engineering polycondensates. This method contained substitution of unreactive end groups of Is and TPA by reacting with dimethyl carbonate and 1, 2-alkanediol or 1, 3-alkanediol respectively, followed by transesterification, cyclization of an alkylene carbonate unit, and polycondensation. Is and TPA were temporarily linked by an unstable alkylene carbonate unit and then underwent cyclization with the elimination of five- or six-membered cyclic carbonate at elevated temperature, leading to a family of poly(isosorbide carbonate- co -isosorbide terephthalate)s with high T g (169–193 °C) and high number-average molecular weights (22 700–28 500 g mol −1 ). The molecular structure of the copolymer was confirmed using 1 H, 13 C and 2D NMR techniques. GC-MS, 1 H NMR and 13 C NMR were used to monitor the molecular structure evolution during the combinatorial polymerization process and a mechanism was proposed. Furthermore, the structure–thermal properties relationship study was also conducted on a range of relevant polyesters.