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Fast Hydrolysis Polyesters with a Rigid Cyclic Diol from Camphor

Authors
Park, Jeong EonHwang, Da YoungChoi, Gwang HoChoi, Kyoung HwanSuh, Dong Hack
Issue Date
Aug-2017
Publisher
American Chemical Society
Citation
Biomacromolecules, v.18, no.8, pp 2633 - 2639
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
Biomacromolecules
Volume
18
Number
8
Start Page
2633
End Page
2639
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/194173
DOI
10.1021/acs.biomac.7b00761
ISSN
1525-7797
1526-4602
Abstract
2,2 : 3,3-Bis (4'-hydroxymethylethylenedioxy)-1,7,7-trimethylbicyclo[2.2.1]heptane, abbreviated as CaG, is a compound obtained by transforming a ketone group to a ketal group with camphorquinone and glycerol. The CaG diol has a complex and rigid structure and two primary hydroxyl groups. A polyester series was synthesized with the CaG diol, ethylene glycol, and dimethyl terephthalate. The polyesters exhibited adequate thermal stability up to nearly 330 degrees C and had a high T-g, which steadily increased from 78 to 129 degrees C as the content of CaG increased. A high proportion of the CaG moiety led to an amorphous region that is susceptible to hydrolysis and promoted degradation of the polyester in acidic conditions. Depending on the proportion of CaG in the polymer, the hydrolytic degradation of the polyesters was adjustable.
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