Donor acceptor type neutral state green polymer bearing pyrrole as the donor unit
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Levent Toppare | Derya Baran | L. Toppare | D. Baran | Abidin Balan | Selin Celebi | Bugra Epik | S. Çelebi | Bugra Epik | Abidin Balan | Derya Baran
[1] E. W. Meijer,et al. Developments in the chemistry and band gap engineering of donor-acceptor substituted conjugated polymers , 2001 .
[2] Stephan Kirchmeyer,et al. Electrochromic Window Based on Conducting Poly(3,4‐ethylenedioxythiophene)–Poly(styrene sulfonate) , 2002 .
[3] S. Horng,et al. Deep blue light-emitting diode based on high molecular weight poly(9,9-dioctylfluorene) with high efficiency and color stability , 2008 .
[4] Y. Tao,et al. Doubly ortho-linked quinoxaline/diphenylfluorene hybrids as bipolar, fluorescent chameleons for optoelectronic applications. , 2006, Journal of the American Chemical Society.
[5] F. Wudl,et al. A Processable Green Polymeric Electrochromic , 2005 .
[6] T. Swager,et al. Conjugated polymer-based chemical sensors. , 2000, Chemical reviews.
[7] R. Silbey,et al. Comparative theoretical study of the doping of conjugated polymers: Polarons in polyacetylene and polyparaphenylene , 1982 .
[8] Fred Wudl,et al. A red, green, and blue (RGB) polymeric electrochromic device (PECD): the dawning of the PECD era. , 2004, Angewandte Chemie.
[9] C. Tanyeli,et al. Synthesis and characterization of a new soluble conducting polymer and its electrochromic devices , 2006 .
[10] W. C. Dautremont-Smith. Transition metal oxide electrochromic materials and displays: a review: Part 1: oxides with cathodic coloration , 1982 .
[11] S. Mutlu,et al. Post-fabrication electric field and thermal treatment of polymer light emitting diodes and their photovoltaic properties , 2009 .
[12] A. R. Tatchell,et al. Vogel's Textbook of Practical Organic Chemistry , 1996 .
[13] Jenq-Neng Hwang,et al. Multicolored Electrochromism in Polymers: Structures and Devices , 2004 .
[14] J. Tarábek,et al. Spectroelectrochemical and potentiometric studies of functionalised electroactive polymers , 2005 .
[15] Y. Yamashita,et al. Single-component organic conductors based on neutral radicals containing the pyrazino-TCNQ skeleton , 1992 .
[16] John R. Reynolds,et al. N-substituted poly(3,4-propylenedioxypyrrole)s: High gap and low redox potential switching electroactive and electrochromic polymers , 2003 .
[17] Y. Yamashita,et al. Design of Narrow-Bandgap Polymers. Syntheses and Properties of Monomers and Polymers Containing Aromatic-Donor and o-Quinoid-Acceptor Units , 1996 .
[18] A. Vogel,et al. Vogel's Textbook of Practical Organic Chemistry , 2003 .
[19] J. Reynolds,et al. Electrochemistry of Poly(3,4‐alkylenedioxythiophene) Derivatives , 2003 .
[20] F. Wudl,et al. A Highly Stable, New Electrochromic Polymer: Poly(1,4‐bis(2‐(3′,4′‐ethylenedioxy) thienyl)‐2‐methoxy‐5‐2″‐ethylhexyloxybenzene) , 2003 .
[21] E. W. Meijer,et al. Band‐Gap Engineering of Donor–Acceptor‐Substituted π‐Conjugated Polymers , 1998 .
[22] L. Toppare,et al. Donor−Acceptor Polymer with Benzotriazole Moiety: Enhancing the Electrochromic Properties of the “Donor Unit” , 2008 .
[23] J. Reynolds,et al. The donor-acceptor approach allows a black-to-transmissive switching polymeric electrochrome. , 2008, Nature materials.
[24] J. Reynolds,et al. Spray Processable Green to Highly Transmissive Electrochromics via Chemically Polymerizable Donor–Acceptor Heterocyclic Pentamers , 2008, Advanced materials.
[25] John R. Reynolds,et al. Enhanced Contrast Dual Polymer Electrochromic Devices , 2002 .
[26] C. Tanyeli,et al. A soluble conducting polymer: 1-Phenyl-2,5-di(2-thienyl)-1H-pyrrole and its electrochromic application , 2006 .
[27] A. Zanelli,et al. New Low-Gap Polymers from 3,4-Ethylenedioxythiophene-Bis-Substituted Electron-Poor Thiophenes. The Roles of Thiophene, Donor−Acceptor Alternation, and Copolymerization in Intrinsic Conductivity , 2004 .
[28] C. Tanyeli,et al. A soluble conducting polymer of 2,5-di(thiophen-2-yl)-1-p-tolyl-1H-pyrrole and its electrochromic device , 2007 .
[29] C. Tanyeli,et al. Electrochromic properties of a soluble conducting polymer of 1-benzyl-2,5-di(thiophene-2-yl)-1H-pyrrole , 2007 .
[30] John R. Reynolds,et al. High Contrast Ratio and Fast-Switching Dual Polymer Electrochromic Devices , 1998 .
[31] H. Sirringhaus,et al. Self-Aligned, Vertical-Channel, Polymer Field-Effect Transistors , 2003, Science.
[32] Helmut Neugebauer,et al. Flexible, long-lived, large-area, organic solar cells , 2007 .
[33] Y. Udum,et al. Both p- and n-type dopable polymer toward electrochromic applications , 2008 .
[34] U. Salzner,et al. Does the Donor−Acceptor Concept Work for Designing Synthetic Metals? 2. Theoretical Investigation of Copolymers of 4-(Dicyanomethylene)-4H-cyclopenta[2,1-b:3,4-b‘]dithiophene and 3,4-(Ethylenedioxy)thiophene , 2002 .
[35] L. Toppare,et al. Processable and multichromic polymer of bis-3-hexylthiophene substituted 4-tert-butylphenyl quinoxaline , 2008 .
[36] Geoffrey M. Spinks,et al. Conductive Electroactive Polymers: Intelligent Materials Systems , 1997 .
[37] A. Neudeck,et al. LIGA-electrodes in voltammetric and spectroelectrochemical studies , 2000, Fresenius' Journal of Analytical Chemistry.
[38] Benjamin D. Reeves,et al. Electrochromic devices based on soluble and processable dioxythiophene polymersElectronic supplementary information (ESI) available: details of the synthesis of PProDOT(CH2OC18H37)2 and PProDOT(CH2OEtHx)2 and their polymerization. See http://www.rsc.org/suppdata/jm/b3/b306365h/ , 2003 .
[39] J. Reynolds,et al. Conducting Poly(3,4-alkylenedioxythiophene) Derivatives as Fast Electrochromics with High-Contrast Ratios , 1998 .
[40] B. D. Malhotra,et al. Electrochromic properties of polycarbazole films , 1997 .
[41] A. Heeger,et al. Synthesis of electrically conducting organic polymers: halogen derivatives of polyacetylene, (CH)x , 1977 .
[42] Levent Toppare,et al. A neutral state green polymer with a superior transmissive light blue oxidized state. , 2007, Chemical communications.