6 results
Search Results
Now showing 1 - 6 of 6
Article Citation - WoS: 94Citation - Scopus: 95A New Conducting Polymer Bearing 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (bodipy) Subunit: Synthesis and Characterization(Pergamon-elsevier Science Ltd, 2008) Cihaner, Atilla; Algi, FatihA new monomer system based on thiophene, pyrrole and 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene dye (SNS-BODIPY) was synthesized and its corresponding polymer (PSNS-BODIPY) was obtained via repetitive cycling or constant potential electrolysis in 0.1 M tetrabutylammonium hexafluorophosphate dissolved in dichloromethane. The PSNS-BODIPY film has very stable and well-defined reversible redox couples during p-doping process. Multi-electrochromic polymer film has a band gap of 2.9 eV with two absorption bands in its neutral state at 351 and 525 nm, attributed to the polymer backbone and BODIPY subunits, respectively. The percentage transmittance changes between both states (neutral and oxidized) were found as 12.1% for 351 nm and 17.7% for 525 nm in the visible region as well as 46.2% for 1050 nm in the near-infrared region. Beyond the robustness, the PSNS-BODIPY film has high redox stability (retaining 53.3% of its electroactivity at 351 nm after 2000 switching) with a low response time of 1.0 s. (C) 2008 Elsevier Ltd. All rights reserved.Article Citation - WoS: 8Citation - Scopus: 8Electropolymerization and Ion Sensitivity of Chemiluminescent Thienyl Systems(Pergamon-elsevier Science Ltd, 2009) Asil, Demet; Cihaner, Atilla; Onal, Ahmet M.Redox driven chemiluminescent (CL) compounds based on thienyl and pyridazine systems, namely 2,3-dihydrothieno(3,4-d)pyridazine-1,4-dione (T-Lum) and 5,7-di-thiophen-2-yl-2,3-dihydrothieno[3,4-d]pyridazine-1,4-dione (TTT-Lum), were synthesized. Soluble compounds both in organic media and basic aqueous solution were found to give CL and electroluminescent (EL) reactions by the treatment of oxidants (H2O2 and KMnO4) and by an external potential pulse on the working electrode, respectively. Furthermore, the CL reaction can be speeded up by Fe3+ ion or blood samples. On the other hand, one of the compounds. TTT-Lum, can be polymerized successfully via electrochemically both in 0.1 M LiClO4/acetonitrile containing 5% of borontrifluoro diethylether (BF3-Et2O) and neat BF3-Et2O solution. The corresponding polymer film (PTTT-Lum) bearing CL units has a very stable and a well-defined reversible redox couple. Also, the electrochromic polymer film has a band gap of 1.74 eV and exhibits EL behavior. (C) 2009 Elsevier Ltd. All rights reserved.Article Citation - WoS: 11Citation - Scopus: 12A Low Band Gap Polymer Based on Selenophene and Benzobis (thiadiazole)(Pergamon-elsevier Science Ltd, 2017) Abdulrazzaq, Mohammed; Ozkut, Merve Icli; Gokce, Gurcan; Ertan, Salih; Tutuncu, Esra; Cihaner, AtillaA new derivative of benzobis(thiadiazole) based donor-acceptor-donor type monomers, namely 4,7-di (selenophen-2-yl)benzo[1,2-c;4,5-c']bis[1,2,5]thiadiazole (SeBTSe), was synthesized and its polymerization was carried out successfully via electrochemical polymerization in an electrolyte solution of 0.1 M tetrabutylammonium hexafluorophosphate dissolved in dichloromethane. The monomer SeBTSe is a deep red chromophore and it has four redox states: one oxidation, one neutral and two reduction states. The electrochemical behaviour of the corresponding polymer called PSeBTSe was studied by cyclic and differential pulse voltammetry. There is a good agreement between electrochemical (0.62-0.66 eV) and optical (0.63 eV) bandgaps of the polymer. Like the monomer, the ambipolar polymer has four redox states and electrochromic properties: gray beige at neutral state, smoky azurite at oxidized state, beige at first reduced state and dark beige at second reduced state. (C) 2017 Elsevier Ltd. All rights reserved.Article Citation - WoS: 44Citation - Scopus: 45A Novel Electrochromic and Fluorescent Polythienylpyrrole Bearing 1,1′-Bipyrrole(Pergamon-elsevier Science Ltd, 2009) Cihaner, Atilla; Mert, Olcay; Demir, Ayhan S.A novel conducting polymer was successfully synthesized via electropolymerization of 1-(1H-pyrrol-1-yl)-2,5-di(thiophen-2-yl)-1H-pyrrole. The electrochemical and electro-optical properties of the corresponding polymer, which was the first example of polymer containing 1,1'-bipyrrole units, were elaborated using electroanalytical and spectroscopic techniques. Cyclic voltammograms and electro-optical studies showed that the polymer has a stable and well-defined reversible redox process as well as electrochromic behavior. The processable polymer film also possessed a yellowish orange light emitter property. (C) 2008 Elsevier Ltd. All rights reserved.Article Citation - WoS: 16Citation - Scopus: 16Electrochemical and Optical Characterization of a Multielectrochromic Copolymer Based on 3,4-Ethylenedioxythiophene and Functionalized Dithienylpyrrole Derivative(Pergamon-elsevier Science Ltd, 2019) Tutuncu, Esra; Ozkut, Merve Icli; Balci, Burcu; Berk, Hasan; Cihaner, AtillaA novel conjugated copolymer, namely poly(3,4-ethylenedioxythiophene-co-1-(3,5-bis(trifluoromethyl)phenyl)-2,5-di(thiophen-2-yl)-1H-pyrrole) (P(EDOT-co-1)) was synthesized via electropolymerization method from a mixture of 3,4-ethylenedioxythiophene and 1-(3,5-bis(trifluoromethyl)phenyl)-2,5-di(thiophen-2-yl)-1H-pyrrole comonomers. The corresponding copolymer has an optical band gap of 1.7 eV and 41% optical contrast at 525 nm with a coloration efficiency of 258 cm(2)/C and 1.4 s switching time. The copolymer has a multi-electrochromic behavior: It has dark purple, purple, gray, green and cyan colors at different oxidation states. Electrochemical stability of P(EDOT-co-1) copolymer was also investigated and it was observed that the copolymer retained 86% of its stability under ambient conditions in the presence of oxygen (without purging the electrolyte solution with any inert gas) according to the current density and 83% according to the deposited charge even after 1000 redox cycles.Article Citation - WoS: 43Citation - Scopus: 45Electrochemical and Optical Properties of New Soluble Dithienylpyrroles Based on Azo Dyes(Pergamon-elsevier Science Ltd, 2009) Cihaner, Atilla; Algi, FatihTwo dithienylpyrroles based on azo dyes, namely 2,5'-dimethyl-[4-(2,5-di-thiophen-2-yl-pyrrol-1-yl)-phenyl]azobenzene (SNS-AB2) and 2,5'- dimethyloxy-[4-(2,5-di-thiophen-2-yl-pyrrol-1-yl)phenyl]azobenzene (SNS-AB3), were synthesized and their corresponding polymers (PSNS-AB2 and PSNS-AB3) were successfully obtained via electropolymerization. The monomers have lower oxidation potentials (0.75 V and 0.80V vs. Ag/AgCl for SNS-AB2 and SNS-AB3, respectively) when compared to their analogous. Both monomers exhibited photoisomerism properties under irradiation at 360 nm. During the irradiation process, for example, the color of SNS-AB3 changes from yellow to greenish yellow. The electroactive polymer films have well defined and reversible redox couples with a good cycle stability in both aqueous and organic solutions. The polymer films also exhibited electrochromic behaviors; color changes from yellowish green to dark green for the PSNS-AB2 (lambda(max) = 435 nm and E-g = 2.31 eV) and from mustard color to green for PSNS-AB3 (lambda(max) = 430nm and E-g = 2.34 eV). Furthermore, the soluble polymers demonstrated different hues of yellow and green colors. (C) 2008 Elsevier Ltd. All rights reserved.
