Cihaner, Atilla

Profile URL
https://hdl.handle.net/20.500.14411/6658
Name Variants
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
0000-0001-7605-2374
Scopus Author ID
55925768200
Turkish CoHE Profile ID
Google Scholar ID
ECKd5ZgAAAAJ
WoS Researcher ID
AAC-9468-2021

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

NO POVERTY1
NO POVERTY
0
Research Products
ZERO HUNGER2
ZERO HUNGER
0
Research Products
GOOD HEALTH AND WELL-BEING3
GOOD HEALTH AND WELL-BEING
1
Research Products
QUALITY EDUCATION4
QUALITY EDUCATION
0
Research Products
GENDER EQUALITY5
GENDER EQUALITY
0
Research Products
CLEAN WATER AND SANITATION6
CLEAN WATER AND SANITATION
1
Research Products
AFFORDABLE AND CLEAN ENERGY7
AFFORDABLE AND CLEAN ENERGY
3
Research Products
DECENT WORK AND ECONOMIC GROWTH8
DECENT WORK AND ECONOMIC GROWTH
0
Research Products
INDUSTRY, INNOVATION AND INFRASTRUCTURE9
INDUSTRY, INNOVATION AND INFRASTRUCTURE
0
Research Products
REDUCED INEQUALITIES10
REDUCED INEQUALITIES
0
Research Products
SUSTAINABLE CITIES AND COMMUNITIES11
SUSTAINABLE CITIES AND COMMUNITIES
0
Research Products
RESPONSIBLE CONSUMPTION AND PRODUCTION12
RESPONSIBLE CONSUMPTION AND PRODUCTION
0
Research Products
CLIMATE ACTION13
CLIMATE ACTION
0
Research Products
LIFE BELOW WATER14
LIFE BELOW WATER
0
Research Products
LIFE ON LAND15
LIFE ON LAND
0
Research Products
PEACE, JUSTICE AND STRONG INSTITUTIONS16
PEACE, JUSTICE AND STRONG INSTITUTIONS
0
Research Products
PARTNERSHIPS FOR THE GOALS17
PARTNERSHIPS FOR THE GOALS
0
Research Products
Documents

101

Citations

2386

h-index

28

Go to Scopus profile
Documents

103

Citations

2273

Go to WoS profile

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

132/156

Supervised MSc Theses

12

Supervised PhD Theses

0

WoS Citation Count

2273

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

JournalCount
Electrochimica Acta15
Journal of Electroanalytical Chemistry13
Turkish Journal of Chemistry6
Dyes and Pigments6
Organic Electronics6
Current Page: 1 / 8

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Scholarly Output Search Results

Now showing 1 - 10 of 121
  • Article
    Citation - WoS: 7
    Citation - Scopus: 9
    Electrochemical Copolymerization of 2-Substituted Thiophene Derivative Linked by Polyether Bridge With Thiophene
    (Elsevier Science Sa, 2005-09) Cihaner, A; Önal, AM
    New 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: 20
    Citation - Scopus: 21
    Electrochemical Behaviour and Electrochemical Polymerization of Fluoro-Substituted Anilines
    (Wiley, 2002-07-02) Cihaner, A; Önal, AM
    The 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: 6
    Citation - Scopus: 7
    An 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, 2020-07) Tutuncu, Esra; Varlik, Bengisu; Kesimal, Busra; Cihaner, Atilla; Ozkut, Merve Icli; Icli Ozkut, Merve
    An 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: 44
    Citation - Scopus: 45
    A Novel Electrochromic and Fluorescent Polythienylpyrrole Bearing 1,1′-Bipyrrole
    (Pergamon-elsevier Science Ltd, 2009-01) 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: 94
    Citation - Scopus: 96
    A New Conducting Polymer Bearing 4,4-difluoro-4-bora-3a,4a-diaza-<i>s</I>-indacene (bodipy) Subunit: Synthesis and Characterization
    (Pergamon-elsevier Science Ltd, 2008-12) Cihaner, Atilla; Algi, Fatih
    A 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.
  • Master Thesis
    Kemilüminesans Bileşiklerin Sentezi ve Metal İyonu Tanıma ve Kan Tespitinde Kullanımları
    (2021) Balcı, Burcu; Cihaner, Atilla
    Lüminesan bileşikler, geniş uygulama alanları sebebiyle son zamanlarda büyük önem kazanmıştır. Ayrıca, kemilüminesan bileşikler, yüksek lüminesans hassasiyetlerinden dolayı analitik kimyada birçok çalışmada kullanılmıştır. Bu tezde elektron verici-alıcı-verici yaklaşımı ile, isimleri 5,8-di(furan-2-il)-2,3-dihidroftalazin-1,4-dion (F2B-Lum), 5,8-di(selenofen-2-il)-2,3- dihidroftalazin-1,4-dion (S2B-Lum) ve 5,7-di(selenofen-2-il)-2,3-dihidrotiyeno[3,4-d] piridazin-1,4-dion (S2T-Lum) olan, yeni bir kemilüminesan bileşik serisi sentezlenmiştir. Yapıları NMR, FTIR ve HRMS teknikleri kullanılarak doğrulanmıştır. Daha sonra, alkali çözeltide (0,1 M NaOH(sulu)) bileşiklerin hidrojen peroksit ile farklı metal iyonları, hemin ve kan örnekleri varlığında kemilüminesans tepkimeleri araştırılmış ve sonuçlar luminol ile karşılaştırılmıştır. Beklendiği gibi, bileşiklerin bakır(II), demir(III) iyonlarına ve kana duyarlı olduğu gözlenmiştir. Yeni luminol türevleri olarak ilgili bileşiklerin, adli bilimde kan bulgularının tespiti için potansiyel adaylar olduğu sonucuna kolaylıkla varılabilir. Ek olarak, bileşiklerin bakır(II) iyonuna duyarlılığı, onları analitik uygulamalarda bakır iyonu tanıma için kullanılabilir hale getirmiştir. Ayrıca, bileşiklerin redoks davranışlarını araştırmak için döngülü voltametri tekniği kullanılmış ve tersinmez yükseltgenme sinyalleri göstermişlerdir. Ayrıca bu bileşikler kullanılarak -1.05 V'luk bir dış potansiyel uygulanarak kare dalga potansiyel yöntemi ile reaktif oksijen türleri tespit edilebilmektedir.Son olarak bileşiklerden S2T-Lum elektrokimyasal olarak başarılı bir şekilde polimerleştirilmiştir. İlgili polimer PS2T-Lum, elektroaktif olduğu ve polimerik yapısında kemilüminesan aktif uzantılar taşıdığı için luminol tipi polimerlerin değerli bir üyesi olabilir.
  • Article
    Citation - WoS: 14
    Citation - Scopus: 17
    NEW EDOT CONTAINING POLYMERS: EFFECT OF RING SIZE ON THE BENZIMIDAZOLE ACCEPTOR
    (Pergamon-elsevier Science Ltd, 2016-01) Cansu-Ergun, E. G.; Onal, A. M.; Cihaner, A.
    In this study, three different benzimidazole (BIm) based acceptor groups bearing cyclohexane, cycloheptane and cyclooctane rings at 2-C position of benzimidazole were synthesized and coupled with ethylenedioxythiophene (EDOT) donor units via Stille cross-coupling reaction. The resulting donor acceptor-donor (DAD) type monomers were examined in terms of their electrochemical and optical behaviors. All three monomers exhibited dual absorption bands due to their donor-acceptor pattern and exhibited one irreversible oxidation peak at about 0.80 V. The monomers were electrochemically polymerized via both potentiostatic and potentiodynamic methods and electro-optical properties of obtained conjugated polymer films were investigated in monomer free electrolytic solution. It was found that the polymer films exhibited quasi-reversible redox behavior due to the doping/dedoping process of the polymers, which was accompanied by a reversible electrochromic behavior. Electrochromic investigations showed that all three polymer films showed similar multichromic behaviors: green in the neutral state, gray in the oxidized state, and brick-red in the reduced state. Their band gap (Eg) values were elucidated utilizing spectroelectrochemical data and it was found to be around 1.18 eV. Furthermore, one of the polymer film was utilized for the construction of transmissive type electrochromic device (ECD) with poly(3,4-ethylenedioxythiophene) (PEDOT). (C) 2015 Elsevier Ltd. All rights reserved.
  • Article
    Citation - WoS: 65
    Citation - Scopus: 67
    An Electrochromic and Fluorescent Polymer Based on 1-(1
    (Elsevier Science Sa, 2008-03) Cihaner, Atilla; Algi, Fatih
    A novel polymer was synthesized by electrochemical polymerization of 1-(1-naphthyl)-2,5-di-2-thienyl-1H-pyrrole (SNS-1-NAPH). The corresponding polymer (PSNS-1-NAPH) was characterized by cyclic voltammetry, FT-IR and UV-vis spectroscopy. The polymer has a very well-defined and reversible redox process in both organic and aqueous solutions. Furthermore, it shows stable electrochromic behavior; yellow in the neutral state, green in the intermediate state and violet in the oxidized state. PSNS-1-NAPH is soluble in common solvents. Although SNS-1-NAPH is almost nonfluorescent, its polymer is a yellow and/or green light emitter. (c) 2007 Elsevier B.V. All rights reserved.
  • Article
    Citation - WoS: 5
    Citation - Scopus: 5
    Designing a Solution Processable Poly(3,4-Ethylenedioxyselenophene) Analogue
    (Amer Chemical Soc, 2018-10-24) Ertan, Salih; Cihaner, Atilla
    A 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: 21
    Citation - Scopus: 21
    Synthesis 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, Atilla
    A 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.