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The synthesis and photoactive properties of cyclic amphiphilic polymers with azobenzene in main chain
Authors:Ganquan Jiang  Lishan Li  Xiaofei Xu  Jinjie Lu  Xing Zhu  Zhengbiao Zhang  Nianchen Zhou  Xiulin Zhu
Institution:State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, People's Republic of China
Abstract:The cyclic amphiphilic polymers with azobenzene in main chain, cyclic azobenzene tetraethylene glycol polystyrene (cyclic‐Azo‐TEG‐PS) with different molecular weights, were successfully synthesized by combining atom transfer radical polymerization (ATRP) and Cu (I)‐catalyzed azide/alkyne cycloaddition (CuAAC). Gel permeation chromatography (GPC), proton nuclear resonance (1H NMR), Fourier transform‐infrared (FT‐IR), and matrix‐assisted laser desorption/ionization time of flight (MALDI‐TOF) mass spectrometry were used to prove the complete conversion from linear polymers to cyclic ones. The thermal properties and photoisomerization behaviors of obtained cyclic polymers have been investigated by comparison with the linear analogues. The cyclic polymer displayed a higher glass transition temperature compared with the linear one, measured by differential scanning calorimetry (DSC). It was found that the trans‐to‐cis and cis‐to‐trans isomerization of cyclic polymers was both slower than that of their respective linear counterparts upon irradiation by UV/visible light. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 1834–1841
Keywords:cyclic amphiphiles  atom transfer radical polymerization  CuAAC “  click”  chemistry  photoreactive effects  polystyrene
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