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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WoS Researcher ID
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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107 results
Scholarly Output Search Results
Now showing 1 - 10 of 107
Article Citation - WoS: 20Citation - Scopus: 21Electrochemical Behaviour and Electrochemical Polymerization of Fluoro-Substituted Anilines(Wiley, 2002) Cihaner, A; Önal, AMThe electrochemical behaviour of three fluoro-substituted aniline monomers, 2-fluoroaniline (2FAN), 3-fluoroaniline (3FAN) and 4-fluoroaniline (4FAN), was investigated in aqueous acidic and organic media by means of cyclic voltammetry (CV) studies. Constant potential electrolysis (CPE) of the monomers in acetonitrile-water mixture (1: 1 by volume) using NaClO4 as supporting electrolyte yielded soluble polymers. The mechanism of electrochemical polymerization was investigated using in situ electron spin resonance (ESR) and in situ UV-VIS spectroscopic techniques for one of the monomers (4FAN). Both CV and in situ LTV-VIS measurements indicated that the polymers obtained are in the emeraldine base form. In situ ESR studies indicated that electrochemical polymerization involves a radical-cation as an intermediate. Characterization of polymer products have been carried out using FTIR and NMR spectroscopic techniques, and thermal behaviour was studied using differential scanning calorimetry (DSC). It was found that conductivity can be imparted to assynthesized polyfluoroanilines via iodine doping. (C) 2002 Society of Chemical Industry.Article Citation - WoS: 5Citation - Scopus: 6An Electrochromic Polymer Based on Cyclopenta[2,1-B;3,4 Effect of a Single Atom Alteration on the Electrochemical and Optical Properties of the Polymer Backbone(Elsevier Science Sa, 2020) Tutuncu, Esra; Varlik, Bengisu; Kesimal, Busra; Cihaner, Atilla; Ozkut, Merve Icli; Icli Ozkut, MerveAn electrochromic polymer, namely "poly(2,6-(3,3-didecyl-3,4-dihydro-2H-thieno [3,4-b] [1,4]dioxepin-6-yl)-4,4-dioctyl-4H-cyclopenta[2,1-b;3,4-b']dithiophene)" (P1), was electrochemically synthesized successfully, and its electrochemical and optical properties were investigated. The band gap of the polymer P1 was calculated as 1.77 eV with -5.45 eV Highest Occupied Molecular Orbital (HOMO) and -3.68 eV Lowest Unoccupied Molecular Orbital (LUMO) energy levels. The polymer P1 is bluish purple when neutralized and highly transparent greenish purple when oxidized. This color change was observed around 1.4 s between its redox states and optical contrast ratio was found to be as 49 % and 53 % with 234 cm(2)/C and 239 cm(2)/C coloration efficiencies at 590 nm and 634 nm, respectively. Moreover, the properties of this polymer were compared to its analogues and also during this comparison the effect of alteration of a single atom in the pendant unit was tried to be understood.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: 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: 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: 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.

