Browsing by Author "Cihaner, Atilla"

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Citation Count: 13
[1,2,5]thiadiazolo[3,4-g]quinoxaline acceptor-based donor-acceptor-donor-type polymers: Effect of strength and size of donors on the band gap
(Wiley, 2017) Gokce, Gurcan; Karabay, Baris; Cihaner, Atilla; Ozkut, Merve Icli; Chemical Engineering
Electrochromic polymers based on [1,2,5]thiadiazolo[3,4-g]quinoxaline acceptor and thiophene, 3,4-ethylenedioxythiophene and 3,3-didecyl-3,4-proylenedioxythiophene donors, namely poly(6,7-diphenyl-4,9-di(thiophen-2-yl)-[1,2,5]thiadiazolo[3,4-g]quinoxaline) (P1), poly(4-(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-9-(2,3-dihydrothieno[3,4-b][1,4]dioxin-7-yl)-6,7-diphenyl-[1,2,5]thiadiazolo[3,4-g]quinoxaline) (P2), and poly(4-(3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepin-6-yl)-9-(3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepin-8-yl)-6,7-diphenyl-[1,2,5]thiadiazolo[3,4-g]quinoxaline) (P3), respectively, were electrochemically and/or chemically synthesized and characterized. Electrochemical and optical properties of the polymers were then investigated. The results, which were obtained electrochemically and optically, indicate that the polymers bearing the same acceptor and different donor units have a band gap range of 0.59-1.24 eV depending on the strength and size of the donor units and band gap determination method. A significant finding in this study was the phenomenon that when the acceptor is physically huge, the general rule that a weak donor would have a high band gap whereas a strong donor would have low band gap can be broken due to the torsional angles/steric hindrances involved with physically large donor molecules. (c) 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017, 55, 3483-3493
Citation Count: 0
Acid/ base doped/ dedoped low band gap polymer
(Amer Chemical Soc, 2016) Karabay, Baris; Gokce, Gurcan; Cihaner, Atilla; Icli Ozkut, Merve; Chemical Engineering
[No Abstract Available]
Citation Count: 11
Ag nanostructures on a poly(3,4-ethylenedioxythiophene) film prepared with electrochemical route: A controllable roughened SERS substrate with high repeatability and stability
(Pergamon-elsevier Science Ltd, 2012) Dogan, Uzeyir; Kaya, Murat; Cihaner, Atilla; Volkan, Murvet; Chemical Engineering
A simple, reliable and reproducible one-step electrochemical method for the preparation of surface-enhanced Raman-active polymer-mediated silver nanoparticles (Ag NPs) on planar indium tin oxide (ITO) coated glass substrates was reported. Poly(3,4-ethylenedioxythiophene) (PEDOT) film was used as a support material for dispersing nanostructured silver nanostructures on the surface homogeneously, since 3,4-ethylenedioxythiophene (EDOT) monomer polymerizes regioregularly. The optical properties and morphologies of the silver substrates have been investigated by ultraviolet-visible (UV-vis) spectroscopy and field emission scanning electron microscopy (FE-SEM). The UV-vis and FE-SEM results revealed that the Ag nanostructures separately appeared on the PEDOT coated ITO after reduction. The effect of the thickness of PEDOT polymer film, reduction potential of silver, the concentration of silver ion solution and the amount of silver particle on the polymer film on the SERS response were studied as well as repeatability and temporal stability of prepared substrates. Brilliant cresyl blue (BCB) has been used as Raman probes to evaluate the properties of the new SERS substrates. Signals collected over multiple spots within the same substrate resulted in a relative standard deviation (RSD) of 9.34%, while an RSD of 11.05% was measured in signals collected from different substrates. The SERS-active substrates were robust and stable which lost only 5.71% of initial intensity after 1 month. (C) 2012 Elsevier Ltd. All rights reserved.
Citation Count: 49
An ambipolar low band gap material based on BODIPY and EDOT
(Elsevier Science Bv, 2009) Algi, Fatih; Cihaner, Atilla; Chemical Engineering
A novel donor-acceptor type conducting polymer based on BODIPY dye as acceptor and EDOT units as donor parts is synthesized electrochemically. The unique combination of BODIPY and EDOT units provides an ambipolar (n- and p-doping processes) low band gap material (4). This is the first example of p-n junction in an organic pi-conjugated material where BODIPY unit is incorporated directly in the main chain. Furthermore, the polymer film exhibits electrochromic behavior upon p-doping: a color change from light violet (neutral) to indigo (oxidized). (C) 2009 Elsevier B.V. All rights reserved.
Citation Count: 33
An ambipolar neutral state green polymeric electrochromic
(Elsevier, 2009) Algi, Fatih; Cihaner, Atilla; Chemical Engineering
The synthesis and properties of highly stable neutral state green polymeric electrochromic, P1, which is based on 5,8-bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-2,3-di(1H-pyrrol-2-yl)quinoxaline were highlighted. P1 exhibits three well-defined absorption bands with a narrow band gap (1.17 eV). The n- and p-doping (ambipolar) processes suggest that P1 is one of the most promising neutral state green polymers and it can be used in supercapacitors as either cathode or anode electrode material. Apart from the stability and the robustness of the polymer film, P1 shows multi-electrochromic behavior; gray-purple in the reduced form and highly transmissive blue color in the oxidized state. (C) 2009 Elsevier B.V. All rights reserved.
Citation Count: 7
Anodic polymerization of 2,5-di-(2-thienyl)-furan in ethanol
(Pergamon-elsevier Science Ltd, 2007) Icli, Merve; Cihaner, Atilla; Oenal, Ahmet A.; Chemical Engineering
Poly(2,5-di-(2-thienyl)-furan) (PSOS) was synthesized via anodic polymerization of 2,5-di-(2-thienyl)-furan (SOS) in ethanol solution containing 0.2 M LiClO4 as supporting electrolyte. The electrochemical and spectroelectrochemical properties were investigated using electroanalytical and UV-vis spectroscopic techniques, respectively. The band gap of the polymer film was found as 2.22 eV and the film was successfully switched between black oxidized state and orange neutral state. Fluorescence and electrochemical impedance spectroscopy (EIS) studies were also performed. (C) 2007 Elsevier Ltd. All rights reserved.
Citation Count: 11
Atomistic Engineering of Chemiluminogens: Synthesis, Properties and Polymerization of 2,3-Dihydro-Pyrrolo[3,4-d]Pyridazine-1,4-Dione Scaffolds
(Springer/plenum Publishers, 2017) Algi, Melek Pamuk; Oztas, Zahide; Tirkes, Seha; Cihaner, Atilla; Algi, Fatih; Chemical Engineering
Two chemiluminescent compounds containing 2,5-di(thien-2-yl)pyrrole and pyridazine units, namely 5,7-di(thiophen-2-yl)-2,3-dihydro-1H-pyrrolo[3,4-d]pyridazine-1,4(6H)-dione (5) and 6-phenyl-5,7-di(thiophen-2-yl)-2,3-dihydro-1H-pyrrolo[3,4-d]pyridazine-1,4(6H)-dione (6), were successfully synthesized and electrochemically polymerized. The compounds have chemiluminescent properties and glow in the presence of hydrogen peroxide in basic medium. The intensity of the glow can be increased dramatically by using Fe3+ ions, hemin (1.0 ppm) or blood samples (1.0 ppm) as catalyst. The compounds 5 and 6 have one well-defined irreversible oxidation peak at 1.08 V and 1.33 V vs Ag/AgCl, respectively. Electrochemical polymerization of both 5 and 6 were carried out successfully by repeating potential scanning in the presence of BF3. Et2O in an electrolyte solution of 0.1 M LiClO4 dissolved in acetonitrile. The electronic band gaps (E-g) of the polymers P5 and P6 were found to be 2.02 eV and 2.16 eV, respectively. On the other hand, the corresponding polymers are electroactive and exhibited electrochromic features.
Citation Count: 67
A blue to highly transmissive soluble electrochromic polymer based on poly(3,4-propylenedioxyselenophene) with a high stability and coloration efficiency
(Royal Soc Chemistry, 2011) Ozkut, Merve Icli; Atak, Samed; Onal, Ahmet M.; Cihaner, Atilla; Chemical Engineering
The optical and electrochemical properties of a regioregular and soluble alkylenedioxyselenophene-based electrochromic polymer, namely poly(3,3-didecyl-3,4-dihydro-2H-selenopheno[3,4-b][1,4] dioxepine (PProDOS-C-10), which is synthesized by electrochemical polymerization, are highlighted. It is noted that this unique polymer has a low band gap (1.58 eV) and is exceptionally stable under ambient atmospheric conditions. Polymer films retain 97% of their electroactivity after 40 000 cycles. The percentage transmittance of a PProDOS-C10 film was found to be 56.4% at 638 nm and 55.8% at 700 nm. Furthermore, this novel soluble PProDOS-C10 polymer shows an electrochromic behavior: a color change from pure blue to a highly transparent state in a low switching time (1.0 s) during oxidation, with high coloration efficiencies (328 cm 2 C-1 at 638 nm and 319 cm(2) C-1 at 700 nm) when compared to its thiophene analogue.
Citation Count: 1
D-A-D type conjugated polymers in dual electrochromic devices tuning from green to blue colors
(Elsevier Science Sa, 2023) Ozkut, Merve Icli; Onal, Ahmet M.; Cihaner, Atilla; Chemical Engineering
In this study, the electrochemical and electro-optical properties of four different dual electrochromic devices were unraveled. In all devices, soluble donor-acceptor-donor (D-A-D) type conjugated electrochromic polymers based on didecyl substituted 3,4-propylenedioxythiophene and heterodiazole analogs were used, and they were coated on ITO electrochemically for the construction of the electrochromic devices. Because all D-A-D polymers and PEDOT are colorful in their neutral states and colorless in their oxidized states, it is possible to observe one -to-one colors of pure two polymers in their electrochromic devices rather than a mixture of colors. It was observed that devices changed their colors from the tunes of green to blue under applied external voltage. Switching times, coloration efficiencies and stabilities of the electrochromic devices were calculated as ranging from 1.0 to 6.0 s, 133-544 cm2/C and 54-91 %, respectively, after 5000 cycles. The P(PSeP-C10)-P(PNP-C10) device showed the highest coloration efficiency (544 cm2/C) as well as the best optical and electrochemical stabilities among the electrochromic devices after 5000 cycles (91 % and 92 %, respectively).
Citation Count: 18
Design and synthesis of new 4,4′-difluoro-4-bora-3a,4a-diaza-s-indacene based electrochromic polymers
(Pergamon-elsevier Science Ltd, 2013) Algi, Melek Pamuk; Tirkes, Seha; Ertan, Salih; Ergun, Emine Gul Cansu; Cihaner, Atilla; Algi, Fatih; Chemical Engineering
Design, synthesis, optical and electrochemical properties of two novel 4,4'-Difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) based donor-acceptor compounds, 1 and 2, are reported in order to elucidate the structure-property relationships in BODIPY based materials. Importantly, these compounds provide opportunity to be used as crosslinkers, since they have three electroactive donor sides. Furthermore, these compounds are polymerized successfully via electrochemical polymerization. The corresponding polymers (P1 and P2) are also characterized by using electrochemical and optical methods in monomer-free electrolyte solutions. It is found that both polymers P1 and P2 exhibit reversible oxidation peaks with half wave potentials of 0.70 V and 0.98 V vs. Ag/AgCl, respectively, and they have low optical band gaps (1.88 eV for P1 and 1.72 eV for P2). It is also noted that the polymers exhibit multielectrochromic properties upon doping: P1 can be switched from pink color in the neutral state to blue color in the oxidized state and P2 can be switched from transmissive pink color when neutralized to transmissive blue color when oxidized. (C) 2013 Elsevier Ltd. All rights reserved.
Citation Count: 6
Design, synthesis, photochromism and electrochemistry of a novel material with pendant photochromic units
(Pergamon-elsevier Science Ltd, 2014) Algi, Melek Pamuk; Cihaner, Atilla; Algi, Fatih; Chemical Engineering
In the present work, the synthesis, photochromism and electrochemistry of a novel material 1, 1-(4-[3,4-bis(2,5-dimethyl-3-thienyl)cyclopent-3-en-1-yl]phenyl)-2,5-di-2-thienyl-1H-pyrrole, with pendant dithienylethene (DTE) photochromic units are described. It should be noted that the system I can be reversibly and efficiently switched between open (1o) and closed (1c) states by light in both solution and in the solid poly(methyl methacrylate) matrix. It is also noteworthy that the two isomers (1o and 1c) of this novel system 1 can be smoothly polymerized on ITO by electrochemical means. Surprisingly, the DTE unit in I does not retain its photochemical switching properties after immobilization onto ITO. The morphology of the polymer film was investigated by AFM analysis. Furthermore, it was found that the polymer exhibited remarkable electrochromic features that can be switched from green in the neutral state to violet state under applied external potentials without disturbing the photochromic units. (C) 2014 Elsevier Ltd. All rights reserved.
Citation Count: 4
Designing a Solution Processable Poly(3,4-ethylenedioxyselenophene) Analogue
(Amer Chemical Soc, 2018) Ertan, Salih; Cihaner, Atilla; Chemical Engineering
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.
Citation Count: 34
A Diverse-Stimuli Responsive Chemiluminescent Probe with Luminol Scaffold and Its Electropolymerization
(Wiley-v C H verlag Gmbh, 2010) Asil, Demet; Cihaner, Atilla; Algi, Fatih; Onal, Ahmet M.; Chemical Engineering
A diverse-stimuli responsive chemiluminescent system, SNS-Lum, and its electropolymerization to give PSNS-Lum, which is the first example of conjugated polymers with pendant luminol arms inducing chemiluminescence in the presence of super oxide radical anion under neutral conditions, are highlighted.
Citation Count: 26
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
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 Count: 143
Donor-Acceptor Polymer Electrochromes with Tunable Colors and Performance
(Amer Chemical Soc, 2010) Icli, Merve; Pamuk, Melek; Algi, Fatih; Onal, Ahmet M.; Cihaner, Atilla; Chemical Engineering
To demonstrate the effect of donor (D) and acceptor (A) units on the structure property relationships of electrochromic polymers, design, synthesis, characterization and polymerization of a series of D A type systems, 1-5, based on thiophene, 3,4-ethylenedioxythiophene, and 3,3-didecyl-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine as D units and 2,1,3-benzoselenadiazole, 2,1,3-benzothiadiazole and 2-decyl-2H-benzo[d][1,2,3]triazole as A units are highlighted. It is found that these units play key roles on the redox behavior, band gap, neutral state color, and the electrochromic performance (stability, optical contrast, coloration efficiency, and switching time) of the system. It is noted that electropolymerization of these D-A systems provides processable low band gap electrochromes, P1-P5, exhibiting high redox stability, coloration efficiency, transmittance and/or contrast ratio and low response time. Furthermore, P1-P5 reflect various hues of blue and green pallets of the RGB color-space in the neutral state. In particular, it is noteworthy that P5 is an excellent blue-to-colorless polymeric electrochrome, which, to our best knowledge, exhibits the highest optical contrast and coloration efficiency among the D A type systems. The panoramic breadth of the neutral state colors and intriguing features of these polymeric materials further confirm that D A approach allows engineering tunable electrochromes, which hold promise for commercialization of polymeric ROB electrochromics.
Citation Count: 22
Effect of fluorine substituted benzothiadiazole on electro-optical properties of donor-acceptor-donor type monomers and their polymers
(Elsevier Sci Ltd, 2020) Cakal, Deniz; Ercan, Yunus Emre; Onal, Ahmet M.; Cihaner, Atilla; Chemical Engineering
A series of trimeric monomers bearing thiophene donor units and fluorinated analogues of benzothiadiazole acceptor units was synthesized via donor-acceptor-donor approach and polymerized electrochemically in order to investigate the effect of fluorine atom on electro-optical properties of both monomers and their corresponding polymers. All monomers exhibited solvatochromic and fluorescent properties. The introduction of fluorine atom into the conjugated backbone increased the oxidation potentials. Upon moving from nonfluorinated to fully fluorinated analogues, the oxidation potential shifts anodically from 1.30 V to 1.7 V. As in the case of monomers, the fluorine atom substitution also resulted in a decrease in the HOMO energy level of the corresponding polymers, leading to an increase in the electrochemical band gap energy (1.71-1.97 eV). This result can be attributed to deviations from planarity and also to decrease in the effective conjugation length. The polymeric film also exhibited electrochromic properties under various external potentials. Switching time and coloration efficiency values decreased with increasing number of fluorine atom substitution.
Citation Count: 14
Effect of furan, thiophene and selenophene donor groups on benzoselenadiazole based donor-acceptor-donor systems
(Elsevier Science Sa, 2016) Karabay, Lutfiye Canan; Karabay, Bads; Karakoy, Merve Serife; Cihaner, Atilla; Chemical Engineering
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 Count: 0
Effect of phthalimide and thieno[3,4-c]pyrrole-4,6,dione acceptors on p-conjugated donor-acceptor-donor monomers: Experimental and theoretical investigations of photophysical and electrochemical properties
(Pergamon-elsevier Science Ltd, 2023) Cakal, Deniz; Arabaci, Elif Demir; Yildirim, Erol; Cihaner, Atilla; Onal, Ahmet M.; Chemical Engineering
In this study, two novel donor-acceptor-donor monomers were synthesized by coupling a phthalimide (PI) acceptor unit with thiophene (T) and ethylenedioxythiophene (EDOT (E)) donor units. These two novel PI-based monomers, namely 2-(2-ethylhexyl)-4,7-di(thiophen-2-yl)isoindoline-1,3-dione (T-PI) and 4,7-bis(2,3-dihydrothieno[3,4-b] [1,4]dioxin-5-yl)-2-(2-ethylhexyl)isoindoline-1,3-dione (E-PI), were fully characterized via UV-vis and fluorescence spectroscopy as well as electrochemical methods, and the results were directly compared with those of previously synthesized thieno[3,4-c]pyrrole-4,6-dione (TPD)-based analogues to report the results for four classes of monomers. In this regard, the ef-fects of different donor groups and structural modifications in the acceptor unit as changed from PI to TPD have been investigated to reveal the precise effect of the donor and acceptor on the optical and electrochemical properties of the monomers. All monomers exhibits an intramolecular charge transfer band in the low energy region due to strong donor and acceptor interactions. The oxidation and reduction potentials of the monomers are found to vary depending on the strengths of both donor and acceptor units. PI-based monomers show more positive oxidation and less negative reduction potentials than TPD-based analogues. Similarly, thiophene-based analogues reveal the same trend in their oxidation and reduction potentials as compared to EDOT-based analogues. Lastly, PI-based monomers could not undergo polymerization via electrochemical method, unlike TPD-based monomers, since the dihedral angle arising between donor and PI acceptor disturbs molecular planarity significantly, as demonstrated by first principle calculations.(C) 2023 Elsevier Ltd. All rights reserved.
Citation Count: 8
Effect of ring size on benzimidazole unit on electro-optical properties of donor-acceptor-donor type monomers and their polymers
(Elsevier Science Sa, 2016) Al-Ogaidi, Saad; Karabay, Bads; Karabay, Lutfiye Canan; Cihaner, Atilla; Chemical Engineering
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 Count: 11
Effect of the donor units on the properties of fluorinated acceptor based systems
(Elsevier Sci Ltd, 2021) Cakal, Deniz; Akdag, Akin; Cihaner, Atilla; Onal, Ahmet M.; Chemical Engineering
A new series of monomers in the donor-acceptor-donor array, namely 5-fluoro-4,7-di(furan-2-yl)benzo[c][1,2,5] thiadiazole (F2BT-F), and 5-fluoro-4,7-di(selenophen-2-yl)benzo[c][1,2,5] thiadiazole (S2BT-F), bearing 5-fluorobenzo[c][1,2,5]-thiadiazole as the acceptor moiety and furan and selenophene as the electron donating groups was synthesized and polymerized electrochemically. To compare heteroatom effect, thiophene analogue of newly synthesized (FBT)-B-2-F and S2BT-F namely, (5-fluoro-4,7-di(thiophen-2-yl)benzo[c][1,2,5] thiadiazole (T2BT-F)) and its corresponding polymer were also synthesized. Effect of donor units on the electrochemical and optical properties of fluorinated acceptor based systems was investigated in terms of the effect of different sized heteroatoms in five-membered rings on the dihedral angle and planarity. Theoretical calculations also suggested a deviation from planarity upon fluorination. Moreover, electrochemically obtained polymers possess low bandgap values (1.62 eV-1.68 eV for PF2BT-F and PS2BT-F, respectively) and exhibited electrochromic properties with relatively low switching times.