| Literature DB >> 26174587 |
Haodi Wang1, Li Zhang1, Binyuan Liu1, Bing Han1, Zhongyu Duan1, Cuiyun Qi1, Dae-Won Park2, Il Kim2.
Abstract
High molecular weight cyclic poly(ε-caprolactone)s (cPCLs) with variable ring size are synthesized via light-induced ring closure of α,ω-anthracene-terminated PCL (An-PCL-An). The ring size of cPCL is tunable simply by adjusting the polymer concentration from 10 to 100 mg mL(-1) in THF. The cyclo-addition via the bimolecular cyclization of An-PC-An is well characterized by a variety of analyses such as (1) H NMR and UV-vis spectroscopies, gel-permeation chromatography, and differential scanning calorimetry. The reversible dimerization of An induced by heating enables the cyclic PCL to have a switchable "on-off" capability. This novel light-induced ring-closure technique can be one of the most powerful candidates for producing various well-defined cyclic polymers in highly concentrated polymer solution.Entities:
Keywords: cyclic polymers; photodimerization; poly(ε-caprolactone); ring-opening polymerization
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Year: 2015 PMID: 26174587 DOI: 10.1002/marc.201500171
Source DB: PubMed Journal: Macromol Rapid Commun ISSN: 1022-1336 Impact factor: 5.734