Browsing by Author "Icli-Ozkut, Merve"

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Citation - WoS: 27
Citation - Scopus: 31
Donor-acceptor polymer electrochromes with cyan color: Effect of alkyl chain length on doping processes
(Elsevier, 2012) Celikbilek, Ozden; Icli-Ozkut, Merve; Algi, Fatih; Onal, Ahmet M.; Cihaner, Atilla; Chemical Engineering; 06. School Of Engineering; 01. Atılım University
A new series of donor-acceptor-donor (D-A-D) type compounds consisting of dialkyl substituted 3,4-propylenedioxythiophene and benzothiadiazole units were synthesized and polymerized chemically and electrochemically to investigate the effect of alkyl chain length on the doping process of the conjugated polymers. It was found that the alkyl chain length plays a key role on both doping processes and the solubility of the polymer. It is also noteworthy that this new series of D-A-D electrochromes transmits or reflects the cyan color of the Cyan-Magenta-Yellow (CMY) color space in the neutral state which can be switched to transmissive grey when oxidized. (C) 2011 Elsevier B.V. All rights reserved.
Citation - WoS: 50
Citation - Scopus: 57
Furan and benzochalcogenodiazole based multichromic polymers via a donor-acceptor approach
(Royal Soc Chemistry, 2013) Icli-Ozkut, Merve; Ipek, Halil; Karabay, Baris; Cihaner, Atilla; Onal, Ahmet M.; Chemical Engineering; 06. School Of Engineering; 01. Atılım University
Two new furan and benzochalcogenodiazole based monomers, namely 4,7-di(furan-2-yl) benzo[c][1,2,5]-selenadiazole (FSeF) and 4,7-di(furan-2-yl) benzo[c][1,2,5]thiadiazole (FSF), were designed and synthesized via a donor-acceptor-donor approach. The monomers were electrochemically polymerized via potentiodynamic or potentiostatic methods. The monomers and their polymers exhibited lower oxidation potentials (1.16 V and 1.06 V for monomers; 0.93 V and 0.80 V for polymers vs. Ag/AgCl) and red shifts of the whole dual-band absorption spectra upon moving from S to Se. Intramolecular charge transfer properties of the monomers and the polymers were demonstrated by using electroanalytical and optical methods. Also, the polymers PFSeF and PFSF were multicolored at different redox states and have low band gaps of 1.43 eV and 1.61 eV, respectively.
Citation - WoS: 23
Citation - Scopus: 25
A Neutral State Yellow To Navy Polymer Electrochrome With Pyrene Scaffold
(Elsevier Science Bv, 2011) Icli-Ozkut, Merve; Cihaner, Atilla; Oztas, Zahide; Algi, Fatih; Cihaner, Atilla; Cihaner, Atilla; Chemical Engineering; Chemical Engineering; 06. School Of Engineering; 01. Atılım University
A new pyrene based soluble polymer, namely poly(3,3-didecyl-6-(1-(3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4] dioxepin-6-yl) pyren-6-yl)-3,4-dihydro-2H-thieno[3,4-b][1,4] dioxepine), P5, which is synthesized by both chemical and electrochemical methods, is highlighted. The polymer shows both electrochromic and fluorescent properties (the emission of yellow (545 nm) and yellowish green light (524 nm) in solid state and in THF solution, respectively). It is noteworthy that P5 has a specific optical band gap (2.2 eV) to reflect the yellow color in the neutral state. Furthermore, the optical and electrochemical features of the polymer were investigated. (C) 2011 Elsevier B. V. All rights reserved.
Citation - WoS: 32
Citation - Scopus: 34
Soluble Alkyl Substituted Poly(3,4-Propylenedioxyselenophene)s: a New Platform for Optoelectronic Materials
(Wiley-blackwell, 2011) Atak, Samed; Icli-Ozkut, Merve; Onal, Ahmet M.; Cihaner, Atilla; Chemical Engineering; 06. School Of Engineering; 01. Atılım University
Optical and electrochemical properties of regiosymmetric and soluble alkylenedioxyselenophene-based electrochromic polymers, namely poly(3,3-dibutyl-3,4-dihydro-2H-seleno pheno [3,4-b][1,4]dioxephine) (PProDOS-C(4)), poly(3,3-dihexyl-3,4-dihydro-2H-selenopheno[3,4-b][1,4]dioxephine) (PProDOS-C(6)), and poly(3,3-didecyl-3,4-dihydro-2H-selenopheno[3,4-b][1,4]dioxephine) (PProDOS-C(10)), are highlighted. It is noted that these unique polymers have low bandgaps (1.57-1.65 eV), and they are exceptionally stable under ambient atmospheric conditions. Polymer films retained 82-97% of their electroactivity after 5000 cycles. The percent transmittance of PProDOS-C(n) (n = 4, 6, 10) films found to be between 55 and 59%. Furthermore, these novel soluble PPro-DOS-C(n) polymers showed electrochromic behavior: a color change form pure blue to highly transparent state in a low switching time (1.0 s) during oxidation with high coloration efficiencies (328-864 cm(2) C(-1)) when compared to their thiophene analogues. (C) 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 49: 4398-4405, 2011
Citation - WoS: 22
Citation - Scopus: 25
Substituent and Heteroatom Effects on the Electrochromic Properties of Similar Systems
(Wiley-blackwell, 2012) Icli-Ozkut, Merve; Cihaner, Atilla; Mersini, Jetmire; Onal, Ahmet M.; Cihaner, Atilla; Cihaner, Atilla; Chemical Engineering; Chemical Engineering; 06. School Of Engineering; 01. Atılım University
Electrochromic polymers called poly(3,4-dihydro-3,3-bis ((naphthalen-1-yl)methyl)-2H-thieno[3,4-b][1,4]dioxepine) (PProDOT-Np-2), poly(3,3-dibenzyl-3,4-dihydro-2H-selenopheno[3,4-b][1,4]dioxepine), and poly(3,3-dibenzyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine) were synthesized electrochemically and the effect of substituents and heteroatoms on the electrochromic properties were investigated for the similar systems. All polymers show electrochromism from a colored state when neutralized to transmissive when oxidized. Although, increasing bulky size (PProDOT-Np-2) causes lower coloration efficiency (CE) as well as lower optical contrast, the replacement of S atom by Se atom resulted in a lower band gap polymer with a higher CE than its thiophene analog. (c) 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 50: 615- 621, 2012