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Now showing 1 - 5 of 5
  • Article
    Citation - WoS: 65
    Citation - Scopus: 67
    An Electrochromic and Fluorescent Polymer Based on 1-(1
    (Elsevier Science Sa, 2008) 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: 45
    Citation - Scopus: 47
    An Electroactive Polymeric Material and Its Voltammetric Response Towards Alkali Metal Cations in Neat Water
    (Pergamon-elsevier Science Ltd, 2008) Algi, Fatih; Cihaner, Atilla
    The syntheses and characterization of a unique system based on thiophene, pyrrole and benzo-15-crown-5 (SNS-Crown) and its corresponding polymer (PSNS-Crown) are reported. Furthermore, selective, clear and reversible voltammetric responses of the conjugated polymer (PSNS-Crown) film towards the alkali series Li+, Na+ and K+ in both neat water and organic media (ethanol) are described. (c) 2008 Elsevier Ltd. All rights reserved.
  • Article
    Citation - WoS: 96
    Citation - Scopus: 99
    A Processable Rainbow Mimic Fluorescent Polymer and Its Unprecedented Coloration Efficiency in Electrochromic Device
    (Pergamon-elsevier Science Ltd, 2008) Cihaner, Atilla; Algi, Fatih
    A processable rainbow mimic fluorescent polymer (PSNSF) based on 1-(9H-fluoren-2-yl)-2,5-di(thiophen-2-yl)-1H-pyrrole (SNSF) was synthesized via electrochemical polymerization in a mixture of ethanol and CH2Cl2 solution containing 0.1 M LiClO4. Characterization was carried out using cyclic voltammetry, UV-vis and F-FAR spectroscopic techniques. Also, an electrochromic device based on PSNSF was studied, which exhibits high coloration efficiency (CE), high redox stability (retaining 98.6% of its optical activity after 4000th switch) and very low response time (less than 0.5 s). (c) 2007 Elsevier Ltd. All rights reserved.
  • Article
    Citation - WoS: 2
    Citation - Scopus: 3
    Impedance Spectroscopy of N-Substituted Oligo-Oxyethylene Polypyrrole Films
    (John Wiley & Sons inc, 2008) Cihaner, Atilla; Onal, Ahmet M.
    The electrochemical properties of neutral (dedoped) and oxidized (doped) poly(1,11-bis(1,1-pyrrole)-3,6,9-trioxaundecane) (poly-I) film electrodes were investigated using cyclic voltammetry and electrochemical impedance spectroscopy (EIS) techniques. Poly-I was deposited on glassy carbon electrode (GCE) from acetonitrile solution containing 5.0 x 10(-3) M 1,11-bis(1,1-pyrrole)-3,6,9-trioxaundecane (I) and 0.1 M LiClO4 supporting electrolyte. Doped poly-I exhibits a single semicircle in its complex-capacitance plots, indicating a single dominant ion transport process, together with high capacitance values. These features make this polymer film a candidate for an energy storage material. Also, poly-I can be a candidate as a sensory material for the detection of Ag+ based on impedance parameters. (C) 2008 Wiley Periodicals, Inc.
  • Article
    Citation - WoS: 11
    Citation - Scopus: 14
    Electrochemical Synthesis of New Conducting Copolymers Containing Pseudo-Polyether Cages With Pyrrole
    (Elsevier Science Sa, 2007) Cihaner, Atilla
    Conducting copolymers have been synthesized via electrochemical oxidation of pyrrole (Py) in the presence of monomer 1, 11 -bis(1,1-pyrrole)-3,6,9-trioxaundecane (I) in an electrolytic solution containing 0.1 M tetrabutylammonium hexafluorophosphate (TBAPF(6)) dissolved in acetonitrile. It is observed that reversible redox behavior of poly(I-co-Py)s shifts to more positive potentials with the increasing amount of I in the comonomer mixture, indicating formation of a copolymer. It is also found that increasing the ratio of I in the comonomer mixture decreases the conductivity of the obtained polymer films. The dark electrical conductivity measurements in the temperature range of 300-100 K revealed the extrinsic type of conduction with activation energy values being in the range of 82.3-16.9 meV. (c) 2007 Elsevier B.V. All rights reserved.