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Article Citation - WoS: 11Citation - Scopus: 14Electrochemical Synthesis of New Conducting Copolymers Containing Pseudo-Polyether Cages With Pyrrole(Elsevier Science Sa, 2007) Cihaner, AtillaConducting copolymers have been synthesized via electrochemical oxidation of pyrrole (Py) in the presence of monomer 1, 11 -bis(1,1-pyrrole)-3,6,9-trioxaundecane (I) in an electrolytic solution containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF(6)) dissolved in acetonitrile. It is observed that reversible redox behavior of poly(I-co-Py)s shifts to more positive potentials with the increasing amount of I in the comonomer mixture, indicating formation of a copolymer. It is also found that increasing the ratio of I in the comonomer mixture decreases the conductivity of the obtained polymer films. The dark electrical conductivity measurements in the temperature range of 300-100 K revealed the extrinsic type of conduction with activation energy values being in the range of 82.3-16.9 meV. (c) 2007 Elsevier B.V. All rights reserved.Article Citation - WoS: 19Citation - Scopus: 19Poly(3,4-Alkylenedioxyselenophene)s: Past, Present, and Future(Georg Thieme verlag Kg, 2015) Cihaner, AtillaBecause of their optical and electronic properties, polythiophenes and their derivatives, especially poly(3,4-alkylenedioxythiophene)s, are among the most promising materials in the field of electrochromic polymers. The properties of these polymers can be tuned by replacing the sulfur atom of the thiophene moiety with a selenium atom, because selenium has a lower electronegativity, a higher metallic character, a larger atomic size, and greater polarizability than sulfur. This approach has opened the door to a new and vibrant class of conjugated polymers. Today 3,4-alkylenedioxyselenophenes are thought as powerful competitors to 3,4-alkylenedioxythiophenes. Here, an overview is presented of poly(3,4-alkylenedioxyselenophene)s, as one of the most attractive groups of conjugated polymers. The design, synthesis, and applications of poly(3,4-alkylenedioxyselenophene)s and their derivatives are discussed in detail and compared with the corresponding features of their thiophene analogues. The electrochemical and electrochromic properties and band gaps of poly(3,4-alkylenedioxyselenophene) s are also discussed in relation to their chemical structures. 1 Introduction 2 Polyselenophenes 3 Poly(3,4-ethylenedioxyselenophene)s 4 Poly(3,4-propylenedioxyselenophene)s 5 ConclusionsArticle Citation - WoS: 6Citation - Scopus: 6Anodic Oxidation of N-Substituted Dipyrrolyl Linked by Polyether Bridge(Taylor & Francis inc, 2006) Cihaner, AtillaElectroactive polymer containing polyether pseudo-cages has been synthesized by anodic oxidation of 1,11-bis(1,1-pyrrole)-3,6,9-trioxaundecane (I) using acetonitrile (ACN) as solvent and tetrabutylammonium perchlorate (TBAClO 4 ) as supporting electrolyte. Electrochemical behavior of monomer I and its polymer, poly-I , were studied using cyclic voltammetry (CV) and UV-VIS spectroscopic techniques. Also, a doping/dedoping study was carried out using electron spin resonance (ESR) and UV-VIS spectroscopic techniques. Thermal behavior of the product was studied using differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA).
