메뉴 건너뛰기




Volumn 123, Issue , 2014, Pages 441-449

Electrochemical and optical properties of new electrochromic and fluorescent nitrobenzoyl polypyrrole derivatives

Author keywords

electrochromism; electropolymerization; fluorescent polymer; nitrobenzoyl pyrrole

Indexed keywords

CYCLIC VOLTAMMETRIC; ELECTROCHEMICAL ROUTES; ELECTROCHROMIC BEHAVIOR; FLUORESCENT POLYMERS; HOMO AND LUMO ENERGIES; NITROBENZOYL PYRROLE; POLYPYRROLE DERIVATIVES; PYRROLE DERIVATIVES;

EID: 84893595054     PISSN: 00134686     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.electacta.2014.01.070     Document Type: Article
Times cited : (17)

References (45)
  • 2
    • 37349073819 scopus 로고    scopus 로고
    • Electrochemical characteristics of poly(3-methyl thiophene)/sulfonated- SEBS composite electrode for polymer battery
    • Y.W. Ju, H.R. Jung, and W.J. Lee Electrochemical characteristics of poly(3-methyl thiophene)/sulfonated-SEBS composite electrode for polymer battery Synth. Met. 157 2007 823
    • (2007) Synth. Met. , vol.157 , pp. 823
    • Ju, Y.W.1    Jung, H.R.2    Lee, W.J.3
  • 3
    • 75649084153 scopus 로고    scopus 로고
    • Color control in π-conjugated organic polymers
    • P.M. Beaujuge, and J.R. Reynolds Color control in π-conjugated organic polymers Chemical Reviews 110 2010 268
    • (2010) Chemical Reviews , vol.110 , pp. 268
    • Beaujuge, P.M.1    Reynolds, J.R.2
  • 5
    • 37349079078 scopus 로고    scopus 로고
    • Polyaniline-related ion-barrier anticorrosion coatings: I. Ionic permeability of polyaniline, cationic, and bipolar films
    • J. Wang, C.C. Torardi, and M.W. Duch Polyaniline-related ion-barrier anticorrosion coatings: I. Ionic permeability of polyaniline, cationic, and bipolar films Synth. Met. 157 2007 846
    • (2007) Synth. Met. , vol.157 , pp. 846
    • Wang, J.1    Torardi, C.C.2    Duch, M.W.3
  • 7
    • 0033620585 scopus 로고    scopus 로고
    • Biomolecule immobilization on electrode surfaces by entrapment or attachment to electrochemically polymerized films
    • S. Cosnier Biomolecule immobilization on electrode surfaces by entrapment or attachment to electrochemically polymerized films Biosensors and Bioelectronics 14 1999 443
    • (1999) Biosensors and Bioelectronics , vol.14 , pp. 443
    • Cosnier, S.1
  • 8
    • 33751072399 scopus 로고    scopus 로고
    • Biomolecular immobilization on conducting polymers for biosensing applications
    • T. Ahuja, I.A., Mir, D., Kumar, Rajesh, Biomolecular immobilization on conducting polymers for biosensing applications, Biomaterials 28 (2007) 791.
    • (2007) Biomaterials , vol.28 , pp. 791
    • Ahuja, T.1    Mir, I.A.2    Kumar Rajesh, D.3
  • 9
    • 0031766333 scopus 로고    scopus 로고
    • New fructose biosensors utilizing a polypyrrole film and d-fructose 5-dehydrogenase immobilized by different processes
    • C.A.B. Garcia, G.D. Neto, and L.T. Kubota New fructose biosensors utilizing a polypyrrole film and d-fructose 5-dehydrogenase immobilized by different processes Anal. Chim. Acta 374 1998 201
    • (1998) Anal. Chim. Acta , vol.374 , pp. 201
    • Garcia, C.A.B.1    Neto, G.D.2    Kubota, L.T.3
  • 10
    • 45849153853 scopus 로고    scopus 로고
    • Effect of electrolyte solvent on the morphology of polypyrrole films: Application to the use of polypyrrole in pH sensors
    • S. Carquigny, O. Segut, B. Lakard, F. Lallemand, and P. Fievet Effect of electrolyte solvent on the morphology of polypyrrole films: Application to the use of polypyrrole in pH sensors Synth. Met. 158 2008 453
    • (2008) Synth. Met. , vol.158 , pp. 453
    • Carquigny, S.1    Segut, O.2    Lakard, B.3    Lallemand, F.4    Fievet, P.5
  • 11
    • 79956337964 scopus 로고    scopus 로고
    • Patterning of conjugated polymers for organic optoelectronic devices
    • Y. Xu, F. Zhang, and X. Feng Patterning of conjugated polymers for organic optoelectronic devices Small 7 2011 1338
    • (2011) Small , vol.7 , pp. 1338
    • Xu, Y.1    Zhang, F.2    Feng, X.3
  • 12
    • 0032860734 scopus 로고    scopus 로고
    • Substituted polythiophenes designed for optoelectronic devices and Conductors
    • M.R. Andersson Substituted polythiophenes designed for optoelectronic devices and Conductors J. Mater. Chem. 9 1999 1933
    • (1999) J. Mater. Chem. , vol.9 , pp. 1933
    • Andersson, M.R.1
  • 13
    • 78650855488 scopus 로고    scopus 로고
    • Investigation of electrochromic properties of poly(3,5-bis(4- methoxyphenyl)dithieno[3,2-b;2′,3′-d]thiophene)
    • O. Sahina, I. Osken, and T. Ozturk Investigation of electrochromic properties of poly(3,5-bis(4-methoxyphenyl)dithieno[3,2-b;2′,3′-d] thiophene) Synth. Met. 161 2011 183
    • (2011) Synth. Met. , vol.161 , pp. 183
    • Sahina, O.1    Osken, I.2    Ozturk, T.3
  • 14
    • 0035810966 scopus 로고    scopus 로고
    • Electrochromic Systems and the Prospects for Devices
    • D.R. Rosseinsky, and R.J. Mortimer Electrochromic Systems and the Prospects for Devices Adv. Mater. 13 2001 783
    • (2001) Adv. Mater. , vol.13 , pp. 783
    • Rosseinsky, D.R.1    Mortimer, R.J.2
  • 15
    • 77957282294 scopus 로고    scopus 로고
    • Combination of donor characters in a donor-acceptor-donor (DAD) type polymer containing benzothiadiazole as the acceptor unit
    • M. Sendur, A. Balan, D. Baran, B. Karabay, and L. Toppare Combination of donor characters in a donor-acceptor-donor (DAD) type polymer containing benzothiadiazole as the acceptor unit Organic Electronics 11 2010 1877
    • (2010) Organic Electronics , vol.11 , pp. 1877
    • Sendur, M.1    Balan, A.2    Baran, D.3    Karabay, B.4    Toppare, L.5
  • 16
    • 79955466144 scopus 로고    scopus 로고
    • Synthesis of new donor-acceptor polymers containing thiadia zoloquinoxaline and pyrazinoquinoxaline moieties: Low-band gap, high optical contrast, and almost black colored materials
    • E.K. Unver et al. Synthesis of new donor-acceptor polymers containing thiadia zoloquinoxaline and pyrazinoquinoxaline moieties: low-band gap, high optical contrast, and almost black colored materials Tetrahedron Letters 52 2011 2725
    • (2011) Tetrahedron Letters , vol.52 , pp. 2725
    • Unver, E.K.1
  • 17
    • 33947713590 scopus 로고    scopus 로고
    • A novel multielectrochromic copolymer based on 1-(4-nitrophenyl)-2,5- di(2-thienyl)-1H-pyrrole and EDOT
    • S. Varis, M. Ak, I.M. Akhmedov, C. Tanyeli, and L. Toppare A novel multielectrochromic copolymer based on 1-(4-nitrophenyl)-2,5-di(2-thienyl)-1H- pyrrole and EDOT J. Electroanal. Chem. 603 2007 8
    • (2007) J. Electroanal. Chem. , vol.603 , pp. 8
    • Varis, S.1    Ak, M.2    Akhmedov, I.M.3    Tanyeli, C.4    Toppare, L.5
  • 18
    • 58249144742 scopus 로고    scopus 로고
    • Electrochemical and optical properties of new soluble dithienylpyrroles based on azo dyes
    • A. Cihaner, and F. AlgI Electrochemical and optical properties of new soluble dithienylpyrroles based on azo dyes Electrochimica Acta 54 2009 1702
    • (2009) Electrochimica Acta , vol.54 , pp. 1702
    • Cihaner, A.1    Algi, F.2
  • 19
    • 0005154738 scopus 로고
    • New electrochemically generated organic conducting polymers
    • G. Tourillon, and F. Garnier New electrochemically generated organic conducting polymers J. Electroanal. Chem. 135 1982 173
    • (1982) J. Electroanal. Chem. , vol.135 , pp. 173
    • Tourillon, G.1    Garnier, F.2
  • 22
    • 80051592521 scopus 로고    scopus 로고
    • Usefulness of aqueous micellar media for electrosynthesis of poly(N-phenylpyrrole). Characterization and optical properties
    • A.K.D. Diawa, D. Gningue-Salla, and J.J. Aaron Usefulness of aqueous micellar media for electrosynthesis of poly(N-phenylpyrrole). Characterization and optical properties Synth. Met. 161 2011 1483
    • (2011) Synth. Met. , vol.161 , pp. 1483
    • Diawa, A.K.D.1    Gningue-Salla, D.2    Aaron, J.J.3
  • 23
  • 25
    • 57749105323 scopus 로고    scopus 로고
    • A novel electrochromic and fluorescent polythienylpyrrole bearing 1,1′-bipyrrole
    • A. Cihaner, O. Mert, and A.S. Demir A novel electrochromic and fluorescent polythienylpyrrole bearing 1,1′-bipyrrole Electrochim. Acta 54 2009 1333
    • (2009) Electrochim. Acta , vol.54 , pp. 1333
    • Cihaner, A.1    Mert, O.2    Demir, A.S.3
  • 26
    • 53649090148 scopus 로고    scopus 로고
    • Processable electrochromic and fluorescent polymers based on N-substituted thienylpyrrole
    • A. Cihaner, and F. AlgI Processable electrochromic and fluorescent polymers based on N-substituted thienylpyrrole Electrochim. Acta 54 2008 665
    • (2008) Electrochim. Acta , vol.54 , pp. 665
    • Cihaner, A.1    Algi, F.2
  • 27
    • 80052591455 scopus 로고    scopus 로고
    • N-substituted 2,5-di(2-thienyl)pyrroles: Application, production, properties, and electrochemical polymerization (review)
    • G.G. Abashev, A.Y. Bushueva, and E.V. Shklyaeva N-substituted 2,5-di(2-thienyl)pyrroles: application, production, properties, and electrochemical polymerization (review) Chemistry of Heterocyclic Compounds 47 2011 130
    • (2011) Chemistry of Heterocyclic Compounds , vol.47 , pp. 130
    • Abashev, G.G.1    Bushueva, A.Y.2    Shklyaeva, E.V.3
  • 29
    • 33747277708 scopus 로고    scopus 로고
    • Electrochromism of dinitrobenzoyl-derivatised polypyrrole films deposited on ITO/glass electrodes
    • A.S. Ribeiro, A.U. Silva, M. Navarro, and J. Tonholo Electrochromism of dinitrobenzoyl-derivatised polypyrrole films deposited on ITO/glass electrodes Electrochim. Acta 51 2006 4892
    • (2006) Electrochim. Acta , vol.51 , pp. 4892
    • Ribeiro, A.S.1    Silva, A.U.2    Navarro, M.3    Tonholo, J.4
  • 31
    • 77956306860 scopus 로고    scopus 로고
    • Synthesis and characterization of poly[(R)-(-) and (S)-(+)-3-(1′- pyrrolyl)propyl-N-(3′',5′'-dinitrobenzoyl)-α-phenylglycinate] s as chiral oligomers of pyrrole
    • J.C. Ramos, J.M.M. Dias, R.M. Souto-Maior, A.S. Ribeiro, J. Tonholo, V. Barbier, J. Penelle, and M. Navarro Synthesis and characterization of poly[(R)-(-) and (S)-(+)-3-(1′-pyrrolyl)propyl-N-(3′',5′'- dinitrobenzoyl)-α-phenylglycinate]s as chiral oligomers of pyrrole Synth. Metals 160 2010 1920
    • (2010) Synth. Metals , vol.160 , pp. 1920
    • Ramos, J.C.1    Dias, J.M.M.2    Souto-Maior, R.M.3    Ribeiro, A.S.4    Tonholo, J.5    Barbier, V.6    Penelle, J.7    Navarro, M.8
  • 32
    • 77951164185 scopus 로고    scopus 로고
    • Indanedione-Substituted Poly(terthiophene)s: Processable Conducting Polymers with Intramolecular Charge Transfer Interactions
    • K. Wagner et al. Indanedione-Substituted Poly(terthiophene)s: Processable Conducting Polymers with Intramolecular Charge Transfer Interactions Macromolecules 43 2010 3817
    • (2010) Macromolecules , vol.43 , pp. 3817
    • Wagner, K.1
  • 34
    • 0031176382 scopus 로고    scopus 로고
    • The cathodic deprotection of the nitrobenzoyl group from phenyl nitrobenzoates in NN-dimethylformamide
    • S.M.A. Jorge, and N.R. Stradiotto The cathodic deprotection of the nitrobenzoyl group from phenyl nitrobenzoates in NN-dimethylformamide J. Electroanal. Chem. 431 1997 237
    • (1997) J. Electroanal. Chem. , vol.431 , pp. 237
    • Jorge, S.M.A.1    Stradiotto, N.R.2
  • 37
    • 0023866120 scopus 로고
    • Optical properties of conducting polymers
    • A.O. Patil, A.J. Heeger, and F. Wudl Optical properties of conducting polymers Chem. Rev. 88 1988 183
    • (1988) Chem. Rev. , vol.88 , pp. 183
    • Patil, A.O.1    Heeger, A.J.2    Wudl, F.3
  • 40
    • 0021093572 scopus 로고
    • Chain-length dependence of electronic and electrochemical properties of conjugated systems: Polyacetylene, polyphenylene, polythiophene, and polypyrrole, J
    • J.L. Bredas, R. Silbey, D.X. Boudreux, and R.R. Chance Chain-length dependence of electronic and electrochemical properties of conjugated systems: polyacetylene, polyphenylene, polythiophene, and polypyrrole, J Am. Chem. Soc. 105 1983 6555
    • (1983) Am. Chem. Soc. , vol.105 , pp. 6555
    • Bredas, J.L.1    Silbey, R.2    Boudreux, D.X.3    Chance, R.R.4
  • 41
    • 0031100005 scopus 로고    scopus 로고
    • Stability of n-type doped conducting polymers and consequences for polymeric microelectronic devices
    • D.M. de Leeuw, M.M.J. Simenon, A.B. Brown, and R.E. Einerhand Stability of n-type doped conducting polymers and consequences for polymeric microelectronic devices Synth. Met. 87 1997 53
    • (1997) Synth. Met. , vol.87 , pp. 53
    • De Leeuw, D.M.1    Simenon, M.M.J.2    Brown, A.B.3    Einerhand, R.E.4
  • 43
    • 84874931447 scopus 로고    scopus 로고
    • Electronic properties of semiconducting naphthalene bisimide derivatives - Ultraviolet photoelectron spectroscopy versus electrochemistry
    • R. Rybakiewicz, P. Gawry, D. Tsikritzis, K. Emmanouil, S. Kennou, M. Zagorska, and A. Pron Electronic properties of semiconducting naphthalene bisimide derivatives - Ultraviolet photoelectron spectroscopy versus electrochemistry Electrochimica Acta 96 2013 13
    • (2013) Electrochimica Acta , vol.96 , pp. 13
    • Rybakiewicz, R.1    Gawry, P.2    Tsikritzis, D.3    Emmanouil, K.4    Kennou, S.5    Zagorska, M.6    Pron, A.7
  • 44
    • 79955831505 scopus 로고    scopus 로고
    • Electrochromic properties of a novel low band gap conjugated copolymer based on 1,4-bis(2-thienyl)-naphthalene and 3,4-ethylenedioxythiophene
    • B. Wang, J. Zhao, C. Cui, R. Liu, J. Liu, H. Wang, and H. Liu Electrochromic properties of a novel low band gap conjugated copolymer based on 1,4-bis(2-thienyl)-naphthalene and 3,4-ethylenedioxythiophene Electrochimica Acta 56 2011 4819
    • (2011) Electrochimica Acta , vol.56 , pp. 4819
    • Wang, B.1    Zhao, J.2    Cui, C.3    Liu, R.4    Liu, J.5    Wang, H.6    Liu, H.7
  • 45
    • 0012099968 scopus 로고
    • Charge storage in doped poly(thiophene): Optical and electrochemical studies
    • T.C. Chung, J.H. Kaufman, A.J. Heeger, and F. Wudl Charge storage in doped poly(thiophene): Optical and electrochemical studies Physical Reviews B 30 1984 702
    • (1984) Physical Reviews B , vol.30 , pp. 702
    • Chung, T.C.1    Kaufman, J.H.2    Heeger, A.J.3    Wudl, F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.