A classified and comparative review of Poly (2,5-dithienyl-N-substituted-pyrrole) derivatives for electrochromic applications

被引:25
作者
Carbas, Buket Bezgin [1 ,2 ]
Ergun, Emine Gul Cansu [1 ,3 ]
机构
[1] Karamanoglu Mehmetbey Univ, Dept Energy Syst Engn, Karaman, Turkey
[2] KaramanogluMehmetbey Univ, Conduct Polymers & Energy Applicat Lab, Karaman, Turkey
[3] Baskent Univ, Dept Elect & Elect Engn, Ankara, Turkey
关键词
5-dithienylpyrrole; SNS; Electrochromism; Conjugated polymer; Electrochromic polymer; SOLUBLE CONDUCTING POLYMER; COLORATION EFFICIENCY; OPTICAL-PROPERTIES; SPECTROELECTROCHEMICAL PROPERTIES; ELECTROCHEMICAL SYNTHESIS; OPTOELECTRONIC PROPERTIES; FLUORESCENCE PROPERTIES; CONJUGATED POLYMERS; HIGH-CONTRAST; PYRROLE;
D O I
10.1016/j.eurpolymj.2022.111363
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(2,5-dithienyl-1-substituted-pyrrole) derivatives are one of the important classes for conducting polymers, exhibiting versatile electrochromic property besides used material in a broad range of smart applications. This review offers an overview of various SNS derivatives, mostly for electrochromic applications. In this compilation, the designed, synthesized and electrochemically and optically characterized conducting polymers of SNS derivatives in the literature up to today have been classified and comparatively discussed. The polymers of the SNS derivatives collected here have been prepared mostly by electrochemical techniques. According to N-substitutions form pyrrole unit, P(SNS) derivatives were grouped into five sections: N- alkyl-, phenyl-, amine/amide, homo/heterocyclic-, and crosslinked substituted derivatives. Each section mainly includes the structure-property relationship and the comparison of the effect of substitutions on the electrochromic properties of the resulting polymers.
引用
收藏
页数:18
相关论文
共 110 条
[1]   Double-layered Black Electrochromic Device with a Single Electrode and Long-Term Bistability [J].
Ah, Chil Seong ;
Song, Juhee ;
Cho, Seong M. ;
Kim, Tae-Youb ;
Kim, Han Na ;
Oh, Ji Yong ;
Chu, Hye Yong ;
Ryu, Hojun .
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, 2015, 36 (02) :548-552
[2]   Synthesis, characterization and optoelectrochemical properties of poly(1,6-bis(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)hexane) and its copolymer with EDOT [J].
Ak, Metin ;
Sahmetlioglu, Ertugrul ;
Toppare, Levent .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2008, 621 (01) :55-61
[3]   An electroactive polymeric material and its voltammetric response towards alkali metal cations in neat water [J].
Algi, Fatih ;
Cihaner, Atilla .
TETRAHEDRON LETTERS, 2008, 49 (21) :3530-3533
[4]   Conjugated microporous polymers for energy storage: Recent progress and challenges [J].
Amin, Kamran ;
Ashraf, Nawal ;
Mao, Lijuan ;
Faul, Charl F. J. ;
Wei, Zhixiang .
NANO ENERGY, 2021, 85 (85)
[5]  
Amit NautiyalM.Q., 2018, Eng. Sci, P70, DOI DOI 10.30919/ES8D776
[6]   A Diverse-Stimuli Responsive Chemiluminescent Probe with Luminol Scaffold and Its Electropolymerization [J].
Asil, Demet ;
Cihaner, Atilla ;
Algi, Fatih ;
Onal, Ahmet M. .
ELECTROANALYSIS, 2010, 22 (19) :2254-2260
[7]   A review study of (bio)sensor systems based on conducting polymers [J].
Ates, Murat .
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2013, 33 (04) :1853-1859
[8]   New conjugated polymerizable pyrrole and 2,5-dithienylpyrrole azobenzene dyes: synthesis and spectroelectrochemical properties [J].
Audebert, P ;
Sadki, S ;
Miomandre, F ;
Hapiot, P ;
Chane-Ching, K .
NEW JOURNAL OF CHEMISTRY, 2003, 27 (05) :798-804
[9]   Conducting Polymers [J].
Awuzie, C. I. .
MATERIALS TODAY-PROCEEDINGS, 2017, 4 (04) :5721-5726
[10]   Color Control in π-Conjugated Organic Polymers for Use in Electrochromic Devices [J].
Beaujuge, Pierre M. ;
Reynolds, John R. .
CHEMICAL REVIEWS, 2010, 110 (01) :268-320