One pot synthesis and characterization of novel poly(ether ester) mutiblock copolymers containing poly(tetramethylene oxide) and poly(ethylene terephthalate)

Literature Information

Publication Date 2013-10-18
DOI 10.1039/C3PY00932G
Impact Factor 5.582
Authors

Weichun Huang, Yingbo Wan, Jianying Chen, Qiaozhen Xu, Xiaohong Li, Xiaoming Yang, Yaowen Li, Yingfeng Tu


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Abstract

We demonstrate here a novel method to synthesize poly(ethylene terephthalate)-block-poly(tetramethylene oxide) multiblock copolymers (PET-b-PTMO-b-PET)x by the one pot melt polymerization of cyclic oligo(ethylene terephthalate)s (COETs) using poly(tetramethylene oxide) (PTMO) as a macroinitiator. Two-dimensional and one-dimensional nuclear magnetic resonance (2D and 1D-NMR) techniques, including 1H–13C Heteronuclear Single Quantum Coherence (HSQC) and 1H–1H Correlation Spectroscopy (COSY), have been used to characterize and reveal the multiblock copolymer structures and absolute molecular weights. It was found that the COETs were consumed completely within 15 minutes, and the molecular weights of the block copolymers increased linearly with reaction time. Based on the polymerization kinetic studies, a two-stage polymerization mechanism is proposed: the ring-opening polymerization of COETs by a PTMO macroinitiator to PET-b-PTMO-b-PET triblock copolymers at the first stage, followed by the in situ condensation polymerization of triblock copolymers to (PET-b-PTMO-b-PET)x multiblock copolymers at the second stage. The structures of the multiblock copolymers are further characterized and confirmed by viscometry and gel permeation chromatography (GPC). These multiblock copolymers show improved thermal stability when compared to PTMO homopolymers, and double crystalline properties from PTMO and PET segments, as revealed by thermogravimetric analysis and differential scanning calorimetry, respectively.

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Contents list

2021-09-01 Front/Back Matter

DOI: 10.1039/D1CP90176A

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