Chemoenzymatic synthesis of sucrose-containing aromatic polymers

被引:0
作者
Park, HG
Chang, HN [1 ]
Dordick, JS
机构
[1] Samsung Adv Inst Technol, Taejon, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Chem Engn & Bioproc Engn, Res Ctr, Yusung Gu, Taejon 305701, South Korea
[3] Rensselaer Polytech Inst, Dept Chem Engn, Troy, NY USA
关键词
protease; chemoenzymatic synthesis; transesterification; sucrose; aromatic polymers;
D O I
10.1002/1097-0290(20010305)72:5<541::AID-BIT1018>3.0.CO;2-C
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A chemoenzymatic approach was developed to prepare sucrose-containing aromatic polymers. The protease from Bacillus licheniformis catalyzed the transesterification of sucrose with a diester of terephthalic acid in pyridine to give the mono- and diester products. At 45 degreesC, >70% of sucrose was consumed after 1 day and sucrose diester began to form after 6 days when >95% of sucrose had been converted to sucrose monoester. The final yield of sucrose diester after 20 days was 13.8%. The sucrose monoester was identified as sucrose 1'-terephthalate and the diester products consisted of sucrose 6,1'-diterephthalate and sucrose 6',1'-diterephthalate in a ratio of 2:1. The sucrose diester products were polymerized with ethylene-glycol and ethylene-diamine to give poly(ethylene-terephthalate) and poly(ethylene-terephthalamide), with sucrose contained in the polymer backbone. The polycondensation reactions were carried out in dimethylsulfoxide (DMSO) at 70 degreesC using zinc acetate as a catalyst. The sucrose-containing polyester and polyamide were obtained at 65% yield for 24 h and at 73% yield for 12 h, respectively. End-group analysis of the polymers by C-13-NMR or H-1-NMR in DMSO provided a number average molecular weight of 3200 and 4300 Da, respectively. Structural analyses of the polymers were performed with H-1-NMR, 13C-NMR, and FTIR. On the basis of 13C-NMR, acylation of the C1', C6, and C6' hydroxyls were maintained in the polymer backbones. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:541 / 547
页数:7
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