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
Job Title
Profesör Doktor
Email Address
atilla.cihaner@atilim.edu.tr
Main Affiliation
Chemical Engineering
Status
Website
ORCID ID
Scopus Author ID
Turkish CoHE Profile ID
Google Scholar ID
WoS Researcher ID
Research Topics
Domains
Physical Sciences
Fields
Materials ScienceEngineeringChemical Engineering
Subfields
Polymers and PlasticsElectrical and Electronic EngineeringBioengineeringMaterials Chemistry
Specific Research Areas
Conducting polymers and applications
Organic Electronics and Photovoltaics
Transition Metal Oxide Nanomaterials
Analytical Chemistry and Sensors
Luminescence and Fluorescent Materials
Sustainable Development Goals
1NO POVERTY
0
Research Products
2ZERO HUNGER
0
Research Products
3GOOD HEALTH AND WELL-BEING
1
Research Products
4QUALITY EDUCATION
0
Research Products
5GENDER EQUALITY
0
Research Products
6CLEAN WATER AND SANITATION
1
Research Products
7AFFORDABLE AND CLEAN ENERGY
3
Research Products
8DECENT WORK AND ECONOMIC GROWTH
0
Research Products
9INDUSTRY, INNOVATION AND INFRASTRUCTURE
0
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10REDUCED INEQUALITIES
0
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11SUSTAINABLE CITIES AND COMMUNITIES
0
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12RESPONSIBLE CONSUMPTION AND PRODUCTION
0
Research Products
13CLIMATE ACTION
0
Research Products
14LIFE BELOW WATER
0
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15LIFE ON LAND
0
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16PEACE, JUSTICE AND STRONG INSTITUTIONS
0
Research Products
17PARTNERSHIPS FOR THE GOALS
0
Research Products
Documents
101
Citations
2386
h-index
28
Documents
103
Citations
2274
Publication Collaboration
| Affiliation Name | Count |
|---|---|
| Atilim University | 105 |
| Middle East Technical University | 60 |
| Çanakkale Onsekiz Mart Üniversitesi | 25 |
| Van Yüzüncü Yıl Üniversitesi | 10 |
| Ankara University | 3 |
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Data obtained from OpenAlex
Scholarly Output
121
Articles
108
Views / Downloads
134/162
Supervised MSc Theses
12
Supervised PhD Theses
0
WoS Citation Count
2274
Scopus Citation Count
2367
Patents
0
Projects
13
WoS Citations per Publication
18.79
Scopus Citations per Publication
19.56
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 |
Current Page: 1 / 8
Scopus Quartile Distribution
Competency Cloud
121 results
Scholarly Output Search Results
Now showing 1 - 10 of 121
Article Citation - WoS: 5Citation - Scopus: 5Designing a Solution Processable Poly(3,4-Ethylenedioxyselenophene) Analogue(Amer Chemical Soc, 2018-10-24) 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, 2009-07) 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, 2010-01) 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, 2006-01) 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, 2005-09) 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: 21Electrochemical Behaviour and Electrochemical Polymerization of Fluoro-Substituted Anilines(Wiley, 2002-07-02) 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: 6Citation - Scopus: 5Synthesis of a regular polymer containing pseudo-polyether cages(Elsevier Science Sa, 2005-04) Cihaner, A; Önal, AMA new compound consisting of 2-thienyl units linked by polyether bridge has been synthesized and its electrochemical polymerization was performed via constant potential electrolysis (CPE) in an electrolytic solution containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF(6)) dissolved in CH3CN. Chemical polymerization was carried out using FeCl3 as oxidizing agent. It is found that both methods gave the same polymer product without any cleavage of the polyether bridge between thiophene (Th) rings. Although as synthesized polymers exhibited no conductivity, they gain conductivity via chemical doping using 12 vapor exposure. The polymers were characterized using FTIR spectroscopic technique and 12 doping was monitored using in-situ electron spin resonance (ESR) spectroscopy. Thermal behavior of electrochemically prepared polymer was investigated using differential scanning calorimetry, DSC and thermogravimetric analysis, TGA. (c) 2005 Elsevier B.V. All rights reserved.Article Citation - WoS: 28Citation - Scopus: 30Functionalized Polysulfide Copolymers With 4-Vinylpyridine Via Inverse Vulcanization(Elsevier Science Bv, 2019-06) Berk, Hasan; Balci, Burcu; Ertan, Salih; Kaya, Murat; Cihaner, AtillaA new series of functional polysulfide copolymers called poly(sulfur-random-4-vinylpyridine) (poly(S-r-4VP)) was synthesized via inverse vulcanization technique by ring opening polymerization of elemental sulfur in the presence of 4-vinylpyridine (4VP). The corresponding copolymers can be post functionalized by using amine group in 4VP unit to get polymers bearing various properties. Elemental sulfur was heated up to 160 degrees C and 4VP was added slowly to a clear yellowish orange colored liquid at this temperature. The reaction mixture was vitrified to form a reddish-brown polymeric material at 180 degrees C in 1 h. The products were characterized by using FTIR, NMR, and Raman spectroscopic techniques. Poly(S-r-4VP) copolymers are soluble in common solvents like dichloromethane, chloroform and tetrahydrofuran. Weight-average molecular weights of poly(S-r-4VP) copolymers with different wt% 4VP were measured by using gel permeation chromatography technique. The polysulfide copolymers with different wt% 4VP have high weight-average molecular weights with polydispersity indeces (PDI) in a range from 1.88 to 4.06 measured by gel permeation chromatography. Post functionalization of the copolymer with 50 wt% 4VP as an example was performed successfully by using alkyl bromide to get N-alkyl quaternized 4VP in polymer backbone.Article Citation - WoS: 1Citation - Scopus: 1Spectroelectrochemical Investigation of the Anodic Oxidation of Dibenzo-18(Elsevier Science Sa, 2004-10) Cihaner, A; Önal, AMPoly(dibenzo-18-crown-6) (poly-DB18C6) was synthesized by electrochemical oxidation of dibenzo-18-crown-6 (DB18C6) using a mixture of acetonitrile and dichloromethane as the solvent and tetrabutylammonium tetrafluoroborate (TBABF(4)) or tetrabutylammonium hexafluorophosphate (TBAPF(6)) as supporting electrolyte. The anodic polymerization of DB18C6 was investigated using in situ ESR and in situ UV-Vis spectroscopic techniques. Spectroelectrochemical (SPEL), properties and thermal analysis of the resulting polymers have been investigated using UV-Vis spectroscopy, differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). (C) 2004 Elsevier B.V. All rights reserved.Article Citation - WoS: 52Citation - Scopus: 57Members of Cmy Color Space: Cyan and Magenta Colored Polymers Based on Oxadiazole Acceptor Unit(Amer Chemical Soc, 2011-12-27) Ozkut, Merve Icli; Algi, Melek Pamuk; Oztas, Zahide; Algi, Fatih; Onal, Ahmet M.; Cihaner, AtillaIn this study, three novel oxadiazole-based polymers were synthesized and their electrochemical and optical properties were investigated. The polymers were found to have both p- and n-type doping properties accompanied by electrochromic response. Two polymer films exhibit cyan and magenta colors, which constitute two legs of CMY color spaces, in their neutral states and they are soluble in common-organic solvents. According to the color mixing theory, all colors in the visible spectrum including black color can be obtained by using these polymers with a yellow colored electrochromic polymer. Among these polymers, the polymer bearing propyledioxythiophene donor units has some superior properties like high stability (it retains 94% of its electroactivity after 2000 cycles), solubility, and high coloration efficiency (230 cm(2)/C), whereas as expected ethylenedioxythiophene containing one has the lowest band gap as 1.08 eV.