UV‐reversible chain extendable polymers from thymine functionalized telechelic polymer chains
Identifieur interne : 003C90 ( Main/Exploration ); précédent : 003C89; suivant : 003C91UV‐reversible chain extendable polymers from thymine functionalized telechelic polymer chains
Auteurs : Gagan Kaur [Australie] ; Arthur Bertrand [France] ; Julien Bernard [France] ; Toby D. M. Bell [Australie] ; Kei Saito [Australie, États-Unis]Source :
- Journal of Polymer Science Part A: Polymer Chemistry [ 0887-624X ] ; 2014-09-15.
Descripteurs français
- Pascal (Inist)
- Acrylate de butyle polymère, Allongement chaîne, Couche mince, Dépolymérisation, Dérivé de la thymine, Etude expérimentale, Photodimérisation, Polymère monodispersé, Polymère photosensible, Polymère téléchélique, Réaction photochimique, Réaction réversible, Réaction état solide, Réactivité chimique.
English descriptors
- KwdEn :
Abstract
The ability of thymine to photodimerize has been exploited to synthesize a reversibly chain‐extendable polymer system. The photopolymerization (>270 nm) of α,ω‐thymine functionalized poly(butyl acrylate) (Thy‐PnBuA‐Thy) oligomers was successfully carried out in the solid film state. These polymers were further successfully depolymerized by using shorter wavelength UV irradiation (<250 nm). These studies demonstrate a novel method to synthesize linear reversibly chain‐extendable polymers based on photodimerization of terminally thymine functionalized oligomers.
Url:
DOI: 10.1002/pola.27282
Affiliations:
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Le document en format XML
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<term>Light sensitive polymer</term>
<term>Monodispersed polymer</term>
<term>Photochemical reaction</term>
<term>Photodimerization</term>
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<term>Solid state reaction</term>
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<term>Thin film</term>
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<term>Polymère photosensible</term>
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<front><div type="abstract">The ability of thymine to photodimerize has been exploited to synthesize a reversibly chain‐extendable polymer system. The photopolymerization (>270 nm) of α,ω‐thymine functionalized poly(butyl acrylate) (Thy‐PnBuA‐Thy) oligomers was successfully carried out in the solid film state. These polymers were further successfully depolymerized by using shorter wavelength UV irradiation (<250 nm). These studies demonstrate a novel method to synthesize linear reversibly chain‐extendable polymers based on photodimerization of terminally thymine functionalized oligomers.</div>
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