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Article Citation - WoS: 25Citation - Scopus: 27A New Processable and Fluorescent Polydithienylpyrrole Electrochrome With Pyrene Appendages(Pergamon-elsevier Science Ltd, 2013) Tirkes, Seha; Mersini, Jetmire; Oztas, Zahide; Algi, Melek Pamuk; Algi, Fatih; Cihaner, AtillaA new hybrid compound, namely 1-(pyren-3-yl)-2,5-di(thiophen-2-yl)-1H-pyrrole (SNS-P), was polymerized via both chemical and electrochemical methods. Chemically obtained soluble polydithienylpyrrole (c-PSNS-P) bearing pyrene appendages is a homogeneous and uniform polymer with a number averaged molecular weight of 15,200 g/mol. The polymer exhibits both multi-electrochromic and fluorescent properties. Upon oxidation, the color of electrochemically obtained polymer (e-PSNS-P) changes from yellowish orange to greenish yellow and to green/blue and finally to blue. In addition, the polymer induces yellowish orange (564 nm) and bright orange emission (613 nm) in solution and solid states, respectively. (C) 2012 Elsevier Ltd. All rights reserved.Article Citation - WoS: 22Citation - Scopus: 25Substituent and Heteroatom Effects on the Electrochromic Properties of Similar Systems(Wiley-blackwell, 2012) Icli-Ozkut, Merve; Cihaner, Atilla; Mersini, Jetmire; Onal, Ahmet M.; Cihaner, Atilla; Cihaner, Atilla; Chemical Engineering; Chemical EngineeringElectrochromic polymers called poly(3,4-dihydro-3,3-bis ((naphthalen-1-yl)methyl)-2H-thieno[3,4-b][1,4]dioxepine) (PProDOT-Np-2), poly(3,3-dibenzyl-3,4-dihydro-2H-selenopheno[3,4-b][1,4]dioxepine), and poly(3,3-dibenzyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine) were synthesized electrochemically and the effect of substituents and heteroatoms on the electrochromic properties were investigated for the similar systems. All polymers show electrochromism from a colored state when neutralized to transmissive when oxidized. Although, increasing bulky size (PProDOT-Np-2) causes lower coloration efficiency (CE) as well as lower optical contrast, the replacement of S atom by Se atom resulted in a lower band gap polymer with a higher CE than its thiophene analog. (c) 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 50: 615- 621, 2012
