Literature DB >> 26174587

Synthesis of High Molecular Weight Cyclic Poly(ε-caprolactone)s of Variable Ring Size Based on a Light-Induced Ring-Closure Approach.

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.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  cyclic polymers; photodimerization; poly(ε-caprolactone); ring-opening polymerization

Mesh:

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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


  1 in total

1.  UV induced reversible chain extension of 1-(2-anthryl)-1-phenylethylene functionalized polyisobutylene.

Authors:  Cimen Ozguc Onal; Turgut Nugay
Journal:  Des Monomers Polym       Date:  2017-10-16       Impact factor: 2.650

  1 in total

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