Cihaner, Atilla
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C.,Atilla
A., Cihaner
C., Atilla
Cihaner A.
A.,Cihaner
Cihaner, Atilla
Cihaner,A.
Atilla Cihaner
Atilla, Cihaner
Cihaner,Atilla
Cihaner, A.
Cihaner, A
A., Cihaner
C., Atilla
Cihaner A.
A.,Cihaner
Cihaner, Atilla
Cihaner,A.
Atilla Cihaner
Atilla, Cihaner
Cihaner,Atilla
Cihaner, A.
Cihaner, A
Job Title
Profesör Doktor
Email Address
atilla.cihaner@atilim.edu.tr
Main Affiliation
Chemical Engineering
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Sustainable Development Goals
1NO POVERTY
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2ZERO HUNGER
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3GOOD HEALTH AND WELL-BEING
1
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4QUALITY EDUCATION
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5GENDER EQUALITY
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6CLEAN WATER AND SANITATION
1
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7AFFORDABLE AND CLEAN ENERGY
3
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8DECENT WORK AND ECONOMIC GROWTH
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9INDUSTRY, INNOVATION AND INFRASTRUCTURE
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10REDUCED INEQUALITIES
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11SUSTAINABLE CITIES AND COMMUNITIES
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12RESPONSIBLE CONSUMPTION AND PRODUCTION
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13CLIMATE ACTION
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14LIFE BELOW WATER
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15LIFE ON LAND
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16PEACE, JUSTICE AND STRONG INSTITUTIONS
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Documents
101
Citations
2366
h-index
28

Documents
103
Citations
2258

Scholarly Output
121
Articles
108
Views / Downloads
558/1849
Supervised MSc Theses
12
Supervised PhD Theses
0
WoS Citation Count
2257
Scopus Citation Count
2347
Patents
0
Projects
13
WoS Citations per Publication
18.65
Scopus Citations per Publication
19.40
Open Access Source
6
Supervised Theses
12
| Journal | Count |
|---|---|
| Electrochimica Acta | 15 |
| Journal of Electroanalytical Chemistry | 13 |
| Turkish Journal of Chemistry | 6 |
| Dyes and Pigments | 6 |
| Organic Electronics | 6 |
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91 results
Scholarly Output Search Results
Now showing 1 - 10 of 91
Article Citation - WoS: 5Citation - Scopus: 5Designing a Solution Processable Poly(3,4-Ethylenedioxyselenophene) Analogue(Amer Chemical Soc, 2018) Ertan, Salih; Cihaner, AtillaA new derivative (EDOS-POSS) of 3,4-ethylenedioxyselenophene integrated with alkyl-substituted polyhedral oligomeric silsesquioxane (POSS) cage was synthesized and characterized. The electroactive monomer was successfully polymerized via both chemical and electrochemical methods. The obtained polymer called PEDOS-POSS was solution-processable and soluble in common organic solvents like tetrahydrofuran, toluene, dichloromethane, and chloroform. PEDOS-POSS polymer exhibited electrochromic behavior: pure blue when neutralized and highly transparent when oxidized. When compared to the parent PEDOS (1.40 eV with lambda(max) = 673 nm), PEDOS-POSS polymer film has a somewhat higher band gap (1.50 eV with lambda(max) = 668 and 724 nm). Also, PEDOS POSS exhibited high optical contrast ratio (59%) and coloration efficiency (593 cm(2)/C for 95% switching) with a low switching time (0.7 s) due to the presence of POSS cage in the polymer backbone. In addition, PEDOS-POSS polymer film was highly robust and stable under ambient conditions (without purging the electrolyte solution with inert gas). Polymer films demonstrated high electrochemical stability; for example, it retained 76% of its electroactivity after 5000 cycles. Furthermore, the polymers exhibited fluorescent properties and exhibited a reddish orange emission centered about at 640 nm. Based on the findings, to the best of our knowledge, it can be concluded that the polymers are the first examples of soluble and fluorescent PEDOS derivatives. These promising properties make PEDOS-POSS polymer a potential material for bioapplications like imaging the cancer cells as well as optoelectronic applications.Article Citation - WoS: 21Citation - Scopus: 21Synthesis and Properties of a Novel Redox Driven Chemiluminescent Material Built on a Terthienyl System(Pergamon-elsevier Science Ltd, 2009) Atilgan, Nurdan; Algi, Fatih; Onal, Ahmet M.; Cihaner, AtillaA novel redox driven chemiluminescent material built on a terthienyl system, namely 5,7-di-ethylenedioxythiophen-2-yl-2,3-dihydro-thieno[3,4-d]pyridazine-1,4-dione (ETE-Lum), which is soluble in both organic media and basic aqueous solution was synthesized and characterized. Furthermore, its polymer, PETE-Lum, which is one of the most rare examples of chemiluminescent polymeric materials bearing a pyridazine unit, was obtained successfully by electrochemical means. Both of the materials give chemiluminescence either by treatment with oxidants (H2O2 and/or KMnO4) or by the application of a potential pulse. (C) 2009 Elsevier Ltd. All rights reserved.Article Citation - WoS: 30Citation - Scopus: 31A New Low-Voltage Polymeric Electrochromic(Elsevier Sci Ltd, 2010) Pamuk, Melek; Tirkes, Seha; Cihaner, Atilla; Algi, FatihDesign, synthesis, and properties of a novel donor-acceptor-donor type low-voltage-driven green polymeric electrochrome, P1, which is based on 8-(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-11-(2,3-dihydrothieno[3,4-b][l,4]dioxin-7-yl)acenaphtho[1,2-b]quinoxaline (1) are highlighted. It is noted that P1 has an ambipolar (n- and p-doping processes) character in 0.1 M tetrabutylammonium hexafluorophosphate/dichloromethame solution and switches to a transmissive blue state upon oxidation. Furthermore, this new polymeric electrochromic candidate exhibits high redox stability, high coloration efficiency and/or contrast ratio, high percent transmittance (%T) and low response time (1.0 s) with a band gap of 1.10 eV-1.25 eV. (C) 2009 Elsevier Ltd. All rights reserved.Article Citation - WoS: 5Citation - Scopus: 5Electrochemical Polymerization of Para-Substituted Haloanilines(Taylor & Francis inc, 2006) Cihaner, A; Önal, AMPolyhaloanilines: poly(4-fluoroaniline) (P4FAN), poly(4-chloroaniline) (P4CAN), and poly(4-bromoaniline) (P4BAN), are synthesized from para-substituted haloaniline monomers; 4-fluoroaniline (4FAN), 4-chloroaniline (4CAN), and 4-bromoaniline (4BAN), respectively, via constant potential electrolysis (CPE) in acetonitrile-water mixture (1:1 v/v) with NaClO4 as supporting electrolyte. Prior to CPE, electrochemical behavior of the monomers were investigated in organic medium utilizing cyclic voltammetry (CV). The course of CPE was monitored using in-situ UV-VIS spectroscopic technique. Characterization of polymer products have been carried out using FT-IR and NMR spectroscopic techniques and thermal behaviors were studied using differential scanning calorimeter (DSC). Polyhaloanilines synthesized by electrochemical oxidation were doped using iodine and the change in the paramagnetic behavior was monitored by ESR, UV-VIS, and FT-IR.Article Citation - WoS: 7Citation - Scopus: 9Electrochemical Copolymerization of 2-Substituted Thiophene Derivative Linked by Polyether Bridge With Thiophene(Elsevier Science Sa, 2005) Cihaner, A; Önal, AMNew conducting copolymers have been synthesized via electrochemical oxidation of thiophene (Th) in the presence of monomer bis(2-thienyl)ethyl (1). Cyclic voltammetry (CV) studies showed that the presence of monomer I in the electrolytic solution greatly changes the CV behaviour of the formation of the polythiophene films. It is found that the increasing ratio of I was found to decrease electroactivity of copoly(I-Th). Electrochemical synthesis of copolymer films was achieved via constant potential electrolysis (CPE) in an electrolytic solution containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF(6)) dissolved in CH3CN. Spectroelectrochemical (SPEL) properties of the films were investigated using UV-vis spectroscopic technique. (C) 2005 Elsevier B.V. All rights reserved.Article Citation - WoS: 20Citation - Scopus: 22Electrochemical and Optical Properties of an Azo Dye Based Conducting Copolymer(Tubitak Scientific & Technological Research Council Turkey, 2009) Cihaner, Atilla; Algi, FatihThe electrochemical and optical properties of a novel conducting copolymer called poly(2,5'-dimethyl-[4-(2,5-di-thiophen-2-yl-pyrrol-1-yl)-phenyl]azobenzene-co-(3,4-ethylenedioxythiophene)) (poly(1-co-EDOT)) are reported. Electrochemically synthesized poly(1-co-EDOT) based on the azo dye has a well-defined and reversible redox couple (0.37 V vs. Ag/AgCl) with good cycle stability. The copolymer film exhibits high conductivity (13 S/cm) as well as electrochromic behavior (magenta when neutralized and transmissive sky blue when oxidized). Furthermore, electro-optically active copolymer film has a low band gap of 1.79 eV with a pi-pi* transition at 555 nm.Article Citation - WoS: 5Citation - Scopus: 5Electrochemical Polymerization of 4-Allylanisole(Pergamon-elsevier Science Ltd, 2001) Cihaner, A; Testereci, HN; Önal, AMElectrochemical polymerization of 3-allylanisole (4AA). via constant potential electrolysis, has been investigated in acetonitrile using two different supporting electrolytes. Redox behavior of the monomer was also studied in the same solvent-electrolyte couples at room temperature. Electrochemical polymerization of the monomer yielded insoluble polymer films on the electrode surface, which bears a very low conductivity, together with the low molecular weight polymers in the bulk of the solution. The decrease in the monomer concentration, during the electrochemical polymerization. was monitored by taking the cyclic voltammogram of the electrolysis solution. The effect of temperature on the rate of electrochemical polymerization was: also studied. The polymers were characterized by taking the H-1-NMR and FTIR spectra. Molecular weight of the soluble polymer was determined by vapor pressure osmometry. Thermal analysis of the polymer film and soluble polymer were done by DSC. (C) 2001 Elsevier Science Ltd. All rights reserved.Article Citation - WoS: 8Citation - Scopus: 8Improvement of Optical Properties and Redox Stability of Poly(3,4-Ethylenedioxythiophene)(Elsevier Sci Ltd, 2018) Ertan, Salih; Cihaner, AtillaIn order to improve the optical properties and redox stability of poly(3,4-ethylenedioxythiophene) (PEDOT) without changing its electrochemical and electrochromic behaviour, it was supported with alkyl-substituted polyhedral oligomeric silsesquioxane (POSS) cage. The corresponding copolymers were obtained electrochemically via potentiostatic or potentiodynamic methods and compared to the parent homopolymers. Electrochemical polymerization of EDOT and POSS containing EDOT called EDOT-POSS in various monomer feed ratios was performed in an electrolyte solution of 0.1 M TBAPF(6) dissolved in a mixture of dichloromethane and acetonitrile (1/3: v/v). Just as PEDOT, the copolymers represented the similar band gap (1.61 eV), redox and electrochromic behaviors. On the other hand, when compared to the parent PEDOT, the presence of POSS cages in the copolymer backbone improved the redox stability and optical properties of PEDOT such as higher percent transmittance change (65% at 621 nm), higher transparency at oxidized state, lower switching time (similar to 1.0 s) and higher coloration efficiency (463 cm(2)/C for 95% switching) as well as higher electrochemical stability (86% of its electroactivity retains after 1750 cycles under ambient conditions).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: 9Citation - Scopus: 11Propylenedioxy and Benzimidazole Based Electrochromic Polymers(Electrochemical Soc inc, 2016) Cansu-Ergun, E. G.; Onal, A. M.; Cihaner, A.In this study, three acceptor units were synthesized by substituting cyclohexane, cycloheptane and cyclooctane rings at 2-C position of benzimidazole. These acceptor units were coupled with dihexyl substituted 3,4-propylenedioxythiophene (PRODOT-C6) donor segments and the resulting donor-acceptor-donor monomers were polymerized via potentiostatic and potentiodynamic methods to obtain their corresponding conjugated polymers (CP). Monomers and their polymers were investigated in terms of the ring size of the substituent on the acceptor unit and their electrochemical and optical behaviors were reported. The monomers exhibited dual absorption bands (at about 310 nm and 520 nm) due to their donor-acceptor pattern. CP films on indium tin oxide conducting substrate were investigated in a monomer free electrolytic solution. The polymer films exhibited quasi-reversible redox behavior due to doping/dedoping which was accompanied by a reversible electrochromic behavior. All three polymer films showed similar multichromic behaviors: green color in the neutral state, gray in the oxidized state, and brick-red in the reduced state. Band gap values (E-g) were elucidated via both electrochemical and optical methods. Moreover, electrochromic device (ECD) was constructed with one of the polymer films (cyclohexane ring bearing benzimidazole and PRODOT-C6 containing polymer) with poly(3,4-ethylenedioxythiophene) (PEDOT). (C) 2016 The Electrochemical Society. All rights reserved.

