2020
DOI: 10.1016/j.synthmet.2020.116545
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A rainbow multielectrochromic copolymer based on 2,5-di(thienyl)pyrrole derivative bearing a dansyl substituent and 3,4-ethylenedioxythiophene

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Cited by 12 publications
(6 citation statements)
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“…A rainbow multielectrochromic copolymer based on 2,5-di(thienyl)pyrrole derivative bearing a dansyl substituent and 3,4-ethylenedioxythiophene was obtained and its spectroelectrochemical properties were studied in [ 127 ]. Polythieno[3,2-b]thiophene with multicolor conversion via embedding EDOT segment was electrosynthesized [ 128 ].…”
Section: Spectroelectrochemical Approach To Study Electroactive Compo...mentioning
confidence: 99%
“…A rainbow multielectrochromic copolymer based on 2,5-di(thienyl)pyrrole derivative bearing a dansyl substituent and 3,4-ethylenedioxythiophene was obtained and its spectroelectrochemical properties were studied in [ 127 ]. Polythieno[3,2-b]thiophene with multicolor conversion via embedding EDOT segment was electrosynthesized [ 128 ].…”
Section: Spectroelectrochemical Approach To Study Electroactive Compo...mentioning
confidence: 99%
“…The end result of the above is electronic and spectral features that respond to modifications of the chemical structure, including variation in emission wavelength, absorption in the visible region, and electrochemical response (Beaujuge & Reynolds, 2010; Ribeiro & Mortimer, 2016; Roncali, 1997). Due to their electrical, magnetic and optical properties, conjugated polymers have found application as the active materials in organic optoelectronic devices, such as electrochromic devices (Neto et al, 2020; Nogueira et al, 2019), solar cells (Rech et al, 2021), organic light emitting diodes (OLEDs) (Yang et al, 2018) and fluorescent sensors (Wang et al, 2020).…”
Section: Nanomaterials To Macromoleculesmentioning
confidence: 99%
“…[31][32][33][34] Furthermore, recently, different approaches have been developed in order to design multi-electrochromic systems, by carrying out the electropolymerization of SNS monomers in the presence of 3,4-ethylendioxythiophene (EDOT). [35][36][37] Commonly, incorporation of such 3,4-alkoxythiophenes provides to the SNS-based polymers a higher chemical and electrochemical stability. [38] This is attributed to the charge stabilization caused by the electron-donating effect of 3,4-dialkoxy substituents.…”
Section: Introductionmentioning
confidence: 99%