Browsing by Author "Karabay, Lutfiye Canan"

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Citation - WoS: 18
Citation - Scopus: 19
Effect of Furan, Thiophene and Selenophene Donor Groups on Benzoselenadiazole Based Donor-Acceptor Systems
(Elsevier Science Sa, 2016) Karabay, Lutfiye Canan; Karabay, Bads; Karakoy, Merve Serife; Cihaner, Atilla
A series of the monomers called 4,7-di(furan-2-yl)benzo[c][1,2,5]selenadiazole (OSeO), 4,7-di(thiophen-2-yl)benzo[c]11,2,5]selenadiazole (SSeS) and 4,7-di(selenophen-2-yl)benzo[c][1,2,5]selenadiazole (SeSeSe) was synthesized via a donor-acceptor-donor (D-A-D) approach. Benzoselenadiazole was used as an acceptor unit and furan, thiophene and selenophene were used as donor units. The effects of chalcogen atoms (0, S, and Se) in furan, thiophene and selenophene were investigated systematically on the properties of the monomers and their corresponding polymers (POSeO, PSSeS and PSeSeSe, respectively), which were polymerized electrochemically via potentiodynamic or potentiostatic methods. The monomers OSeO, SSeS and SeSeSe exhibited low oxidation potentials of 1.15, 1.25 and 1.19 V vs. Ag/AgCl, respectively. Intramolecular charge transfer interaction between donor and acceptor units was demonstrated from the emission spectra of the monomers. Also, the optical studies showed that the ambipolar and electrochromic polymers POSeO, PSSeS and PSeSeSe have low band gaps of 1.57, 1.47 and 1.45 eV, respectively. (C) 2016 Elsevier B.V. All rights reserved.
Citation - WoS: 9
Citation - Scopus: 10
Effect of Ring Size on Benzimidazole Unit on Electro-Optical Properties of Donor-Acceptor Type Monomers and Their Polymers
(Elsevier Science Sa, 2016) Al-Ogaidi, Saad; Karabay, Bads; Karabay, Lutfiye Canan; Cihaner, Atilla
A new series of fluorescent donor-acceptor-donor (D-A-D) type monomers based on benzimidazole acceptor unit bearing various cycloalkane appendages, called 4,7-di-2,3-dihydrothieno[3,4-b] [1,4]dioxin-5-ylspiro[benzimidazole-2,1'-cyclopentane] (E5E), 4,7-di-2,3-dihydrothieno[3,4-b] [1,4]dioxin-5-ylspiro[benzimidazole-2,1'-cyclohexane] (E6E) and 4,7-di-2-thienylspiro[benzimidazole-2,1'-cyclohexane] (T6T), were synthesized and polymerized via potentiostatic and potentiodynamic methods. The effect of ring size on benzimidazole unit and the kind of donor moiety in D-A-D system on the electrochemical and optical properties have been studied systematically. The optical studies showed that the ring size of the benzimidazole unit has no effect on the absorbance and fluorescence properties, whereas the oxidation potential of the E5E, E6E and T6T monomers varied with respect to both the ring size and the kind of donor unit: 0.89 V, 0.83 V and 122 V vs Ag/AgCl, respectively. All polymers have ambipolar (p- and n-type doping) and electrochromic properties. While the polymer films PE5E and PE6E are green at neutral state and transparent at oxidized state, the polymer PT6T has no appreciable color change between its neutral and oxidized states. The polymers PE5E and PE6E bearing 3,4-ethylenedioxythiophene unit as donor units exhibited lower band gap values (1.21 eV and 1.18 eV, respectively) than the polymer PT6T (1.53 eV). When compared to PT6T, PE5E and PE6E polymers are more stable under ambient condition. While PE5E retained 76% of its electroactivity after 4000 cycles, PE6E has 65% of its electroactivity after 2000 cycles. (C) 2016 Elsevier B.V. All rights reserved.
Citation - WoS: 50
Citation - Scopus: 50
Elemental Sulfur-Based Polymeric Materials: Synthesis and Characterization
(Wiley-blackwell, 2016) Salman, Mohamed Khalifa; Karabay, Baris; Karabay, Lutfiye Canan; Cihaner, Atilla
New elemental sulfur-based polymeric materials called poly(sulfur-random-divinylbenzene) [poly(S-r-DVB)] were synthesized by ring opening polymerization via inverse vulcanization technique in the presence of a mixture of o-, m-, and p-diviniylbenzene (DVB) as a cross-linker. A clear yellow/orange colored liquid was obtained from the elemental sulfur melted at 160 degrees C and then by adding various amounts of DVB to this liquid directly via a syringe at 200 degrees C viscous reddish brown polymeric materials were obtained. The copolymers are soluble in common solvents like tetrahydrofuran, dichloromethane, and chloroform, and they can be coated on any surface as a thin film by a spray coating technique. The characterization of the materials was performed by using nuclear magnetic resonance, fourier transform infrared, and Raman spectroscopies. The morphological properties were monitored via scanning electron microscope technique. Thermal analysis showed that an increase in the amount of DVB in the copolymers resulted in an increase in the thermal decomposition temperature. On the other hand, poly(S-r-DVB) copolymers exhibited good percent transmittance as 50% T between 1500 and 13,000 nm in electromagnetic radiation spectrum, which makes them good candidates to be amenable use in military and surveillance cameras. (c) 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016, 133, 43655.
Citation - WoS: 1
Citation - Scopus: 1
Synthesis and Characterization of New Dithienosilole Based Copolymers
(Electrochemical Soc inc, 2016) Karabay, Lutfiye Canan; Al-Jumaili, Mohammed; Cihaner, Atilla
2-Ethylhexyl substituted dithienosilole based soluble polymers including thiophene (1) and bithiophene (2) units were synthesized via Stille coupling reaction. The presence of 2-ethylhexyl substituents on the silole ring gave solubility property to the polymers in common solvents. According to gel permeation chromatography measurements, the weight average molecular weights of the polymers 1 and 2 were found to be as 70,977 with a polydispersity index of 2.30 and 110,439 with a PDI of 1.42, respectively. Fluorescent polymers in toluene solution have maximum emisssion bands at 634 nm for the polymer 1 and 613 nm for the polymer 2. Chemical and electrochemical doping of the polymers in the solution and in the film forms were monitored by using ultraviolet-visible spectroscopic technique. The polymers exhibited chromic (chemochromic and electrochromic) properties. While the colors of the neutral polymer films are purple for the polymer 1 and reddish brown for the polymer 2, both polymers are transparent sky blue at their oxidized states. The bandgaps of polymers in film forms were calculated as 1.81 eV for the polymer 1 and 1.92 eV for the polymer 2. Also, electrochromic device applications of the polymers were done. Electrochemical and optical behaviors of the polymers demonstrated that they can be good candidates for optoelectronic applications. (C) 2016 The Electrochemical Society. All rights reserved.