Effects of substitution position on electrochemical, electrochromic, optical, and photoresponsive properties of azobenzenecarboxylic acid alkyl ester derivatives

被引:18
作者
Tang, Qian [1 ]
He, Li-hua [1 ]
Yang, Yue-hong [1 ]
Long, Jun-fei [1 ]
Fu, Xiang-Kai [1 ]
Gong, Cheng-bin [1 ]
机构
[1] Southwest Univ, Coll Chem & Chem Engn, Key Lab Appl Chem Chongqing Municipal, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochromic materials; Azobenzenecarboxylic acid alkyl ester derivatives; Electrochromic devices; Photoisomerization; Effects of substitution position; FLUORESCENCE PROPERTIES; POLYMERS; VIOLOGEN; SCIENCE; SYSTEMS; COLOR;
D O I
10.1016/j.orgel.2015.11.010
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This study aimed to investigate the effects of substitution position on the electrochemical, electrochromic, optical, and photoresponsive properties of azobenzenecarboxylic acid alkyl ester derivatives. Therefore, a series of azobenzenen ester derivatives, including azobenzene-4,4'-dicarboxylic acid dialkyl ester derivatives (ADDEDs), azobenzene-3,3'-dicarboxylic acid dialkyl ester derivatives (ADADEs), and azobenzene-3,3',5,5'-tetracarboxylic acid four alkyl ester derivatives (ATFAEDs), was synthesized in this work, and their electrochemical, electrochromic, optical, and photoresponsive properties were characterized. Substitution position significantly influenced the electrochemical, electrochromic, and optical properties but not the photoresponsive properties of azobenzenecarboxylic acid alkyl ester derivatives. With regard to stability and response time, the electrochromic properties of azobenzenecarboxylic acid alkyl ester derivatives decreased in the following order: ADDEDs > ATFAEDs > ADADEs. However, ADDEDs, ADADEs, and ATFAEDs can all be reversibly and efficiently photoswitched between trans and cis states upon alternate irradiation at 365 and 440 nm under electrochromic conditions. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:200 / 206
页数:7
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