2011
DOI: 10.1016/j.electacta.2010.11.052
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Multichromic polymers of benzotriazole derivatives: Effect of benzyl substitution

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Cited by 20 publications
(6 citation statements)
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“…The difference between N2-substituted 29 and N1-substituted 30 was even more dramatic when thiophene was the donor group. 58 Neither of the N1-substituted polymers showed tendency for n-type doping in the working potential range due to the change in the effective conjugation length of acceptor unit which hindered the negative charge carrier formation on polymer backbone.…”
Section: Electrochromics (Ecs)mentioning
confidence: 99%
“…The difference between N2-substituted 29 and N1-substituted 30 was even more dramatic when thiophene was the donor group. 58 Neither of the N1-substituted polymers showed tendency for n-type doping in the working potential range due to the change in the effective conjugation length of acceptor unit which hindered the negative charge carrier formation on polymer backbone.…”
Section: Electrochromics (Ecs)mentioning
confidence: 99%
“…Due to their advantages of low cost synthesis, easy derivatization and impeccable integration into many electronic devices, p-conjugated conducting polymers (CPs) have attracted great attention over the last decade. CPs have been frequently used in a wide range of industrial applications including organic light emitting diodes (OLEDs), 1,2 field effect transistors (FETs), 3,4 electrochromic devices, [5][6][7] sensors, 8,9 organic photovoltaics (OPVs), [10][11][12] and supercapacitors (SCs). [13][14][15][16] Particularly, the use of CPs as electrochromic materials has been widely investigated since p-conjugated conducting polymers exhibit reversible and steady color changes at low potentials, high optical contrast in visible and near infra-red (NIR) regions and have high coloriation efficiency and fast switching times.…”
Section: Introductionmentioning
confidence: 99%
“…Since previous studies showed that triazole enhances the proton conductivity with respect to imidazole, it is expected that benzotriazole also presents higher proton conductivity than benzimidazole. Also, the presence of a pendant group bonded to a nitrogen atom of benzotriazole ring create two N‐1 and N‐2 regioisomers, which present different optical and electrochemical behavior . Moreover, small structural variations at the monomers should be considered since they can fine‐tune the electron and proton conductivity properties of the resulting materials.…”
Section: Resultsmentioning
confidence: 99%