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Volumn 12, Issue 10, 2011, Pages 1625-1631

The effect of the donor unit on the optical properties of polymers

Author keywords

Electrochemical polymerization; Multichromism; Optical properties

Indexed keywords

CYCLIC VOLTAMMETRY; ELECTROPOLYMERIZATION; ENERGY GAP; MONOMERS; THIOPHENE;

EID: 79960439175     PISSN: 15661199     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.orgel.2011.06.004     Document Type: Article
Times cited : (23)

References (28)
  • 2
    • 0036378739 scopus 로고    scopus 로고
    • Electrochemistry, polymers and opto-electronic devices: A combination with a future
    • M. De Paoli, and W.A. Gazotti Electrochemistry, polymers and opto-electronic devices: a combination with a future J. Braz. Chem. Soc. 13 2002 410
    • (2002) J. Braz. Chem. Soc. , vol.13 , pp. 410
    • De Paoli, M.1    Gazotti, W.A.2
  • 3
    • 0032677684 scopus 로고    scopus 로고
    • Organic electrochromic materials
    • R.J. Mortimer Organic electrochromic materials Electrochim. Acta 44 1999 2971
    • (1999) Electrochim. Acta , vol.44 , pp. 2971
    • Mortimer, R.J.1
  • 5
    • 43849099242 scopus 로고    scopus 로고
    • Both p- and n-type dopable polymer toward electrochromic applications
    • Y.A. Udum, A. Durmus, E.G. Gunbas, and L. Toppare Both p- and n-type dopable polymer toward electrochromic applications Org. Electron. 9 2008 501
    • (2008) Org. Electron. , vol.9 , pp. 501
    • Udum, Y.A.1    Durmus, A.2    Gunbas, E.G.3    Toppare, L.4
  • 6
    • 0000769761 scopus 로고    scopus 로고
    • Infrared switching electroemissive devices based on highly conducting polymers
    • P. Topart, and P. Hourquebie Infrared switching electroemissive devices based on highly conducting polymers Thin Solid Films 352 1999 243
    • (1999) Thin Solid Films , vol.352 , pp. 243
    • Topart, P.1    Hourquebie, P.2
  • 7
    • 1242331910 scopus 로고    scopus 로고
    • Organic polymeric electrochromic devices: Polychromism with very high coloration efficiency
    • G. Sonmez, H. Meng, and F. Wudl Organic polymeric electrochromic devices: polychromism with very high coloration efficiency Chem. Mater. 16 2004 574
    • (2004) Chem. Mater. , vol.16 , pp. 574
    • Sonmez, G.1    Meng, H.2    Wudl, F.3
  • 8
    • 0001065759 scopus 로고    scopus 로고
    • High contrast ratio and fast-switching dual polymer electrochromic devices
    • S.A. Sapp, G.A. Sotzing, and J.R. Reynolds High contrast ratio and fast-switching dual polymer electrochromic devices Chem. Mater. 10 1998 2101
    • (1998) Chem. Mater. , vol.10 , pp. 2101
    • Sapp, S.A.1    Sotzing, G.A.2    Reynolds, J.R.3
  • 9
    • 0001446739 scopus 로고    scopus 로고
    • Conducting poly(3,4-alkylenedioxythiophene) derivatives as fast electrochromics with high-contrast ratios
    • A. Kumar, D.M. Welsh, M.C. Morvant, F. Piroux, K.A. Abboud, and J.R. Reynolds Conducting poly(3,4-alkylenedioxythiophene) derivatives as fast electrochromics with high-contrast ratios Chem. Mater. 10 1998 896
    • (1998) Chem. Mater. , vol.10 , pp. 896
    • Kumar, A.1    Welsh, D.M.2    Morvant, M.C.3    Piroux, F.4    Abboud, K.A.5    Reynolds, J.R.6
  • 10
    • 10444238106 scopus 로고    scopus 로고
    • Red, green, and blue colors in polymeric electrochromics
    • G. Sonmez, H.B. Sonmez, C.K.F. Shen, and F. Wudl Red, green, and blue colors in polymeric electrochromics Adv. Mater. 16 2004 1905
    • (2004) Adv. Mater. , vol.16 , pp. 1905
    • Sonmez, G.1    Sonmez, H.B.2    Shen, C.K.F.3    Wudl, F.4
  • 11
    • 0033803607 scopus 로고    scopus 로고
    • In situ colorimetric analysis of electrochromic polymers and devices
    • B.C. Thompson, P. Schottland, K. Zong, and J.R. Reynolds In situ colorimetric analysis of electrochromic polymers and devices Chem. Mater. 12 2000 1563
    • (2000) Chem. Mater. , vol.12 , pp. 1563
    • Thompson, B.C.1    Schottland, P.2    Zong, K.3    Reynolds, J.R.4
  • 12
    • 0035867424 scopus 로고    scopus 로고
    • In situ colorimetric analysis of electrochromic polymer films and devices
    • B.C. Thompson, P. Schottland, G. Sonmez, and J.R. Reynolds In situ colorimetric analysis of electrochromic polymer films and devices Synth. Met. 119 2001 333
    • (2001) Synth. Met. , vol.119 , pp. 333
    • Thompson, B.C.1    Schottland, P.2    Sonmez, G.3    Reynolds, J.R.4
  • 13
    • 3042737262 scopus 로고    scopus 로고
    • Green, and blue (RGB) polymeric electrochromic device (PECD): The dawning of the PECD era
    • G. Sonmez, C.K.F. Shen, Y. Rubin, F. Wudl, and A. Red Green, and blue (RGB) polymeric electrochromic device (PECD): the dawning of the PECD era Angew. Chem. Int. Edit. 43 2004 1498
    • (2004) Angew. Chem. Int. Edit. , vol.43 , pp. 1498
    • Sonmez, G.1    Shen, C.K.F.2    Rubin, Y.3    Wudl, F.4    Red, A.5
  • 15
    • 17244379019 scopus 로고    scopus 로고
    • The unusual effect of bandgap lowering by C60 on a conjugated polymer
    • G. Sonmez, C.K.F. Shen, Y. Rubin, and F. Wudl The unusual effect of bandgap lowering by C60 on a conjugated polymer Adv. Mater. 17 2005 897
    • (2005) Adv. Mater. , vol.17 , pp. 897
    • Sonmez, G.1    Shen, C.K.F.2    Rubin, Y.3    Wudl, F.4
  • 16
    • 41549159469 scopus 로고    scopus 로고
    • Processable and multichromic polymer of bis-3-hexylthiophene substituted 4-tert-butylphenyl quinoxaline
    • F. Ozyurt, E.G. Gunbas, A. Durmus, and L. Toppare Processable and multichromic polymer of bis-3-hexylthiophene substituted 4-tert-butylphenyl quinoxaline Org. Electron. 9 2008 296
    • (2008) Org. Electron. , vol.9 , pp. 296
    • Ozyurt, F.1    Gunbas, E.G.2    Durmus, A.3    Toppare, L.4
  • 18
    • 0035867956 scopus 로고    scopus 로고
    • Peierls bond distortion in substituted polyacetylenes
    • C.Q. Wu, Y.G. Zhang, and H.Q. Lin Peierls bond distortion in substituted polyacetylenes Synth. Met. 119 2001 219
    • (2001) Synth. Met. , vol.119 , pp. 219
    • Wu, C.Q.1    Zhang, Y.G.2    Lin, H.Q.3
  • 19
    • 77956493088 scopus 로고    scopus 로고
    • The effect of changes in π-conjugated terthienyl systems using thienyl and ethylenedioxybenzene functionalized thieno[3,4b] pyrazine precursors: Multicolored low band gap polymers
    • S. Tarkuc, E.K. Unver, Y.A. Udum, C. Tanyeli, and L. Toppare The effect of changes in π-conjugated terthienyl systems using thienyl and ethylenedioxybenzene functionalized thieno[3,4b] pyrazine precursors: multicolored low band gap polymers Electrochim. Acta 55 2010 7254
    • (2010) Electrochim. Acta , vol.55 , pp. 7254
    • Tarkuc, S.1    Unver, E.K.2    Udum, Y.A.3    Tanyeli, C.4    Toppare, L.5
  • 20
    • 77950551107 scopus 로고    scopus 로고
    • Effect of conjugated core building block dibenzo[a,c]phenazine unit on p-conjugated electrochromic polymers: Red-shifted absorption
    • E.K. Unver, S. Tarkuc, Y.A. Udum, C. Tanyeli, and L. Toppare Effect of conjugated core building block dibenzo[a,c]phenazine unit on p-conjugated electrochromic polymers: red-shifted absorption J. Polym. Sci., Part A: Polym. Chem. 48 2010 1714
    • (2010) J. Polym. Sci., Part A: Polym. Chem. , vol.48 , pp. 1714
    • Unver, E.K.1    Tarkuc, S.2    Udum, Y.A.3    Tanyeli, C.4    Toppare, L.5
  • 21
    • 37049089033 scopus 로고
    • The chemistry of organolead(IV) tricarboxylates. Synthesis and electrophilic heteroarylation reactions of 2- and 3-thienyl-, and 2- and 3-furyl-lead tricarboxylates
    • J.T. Pinhey, and E.G. Roche The chemistry of organolead(IV) tricarboxylates. Synthesis and electrophilic heteroarylation reactions of 2- and 3-thienyl-, and 2- and 3-furyl-lead tricarboxylates J. Chem. Soc. Perkin Trans. 1 1988 2415
    • (1988) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 2415
    • Pinhey, J.T.1    Roche, E.G.2
  • 22
    • 24144465858 scopus 로고    scopus 로고
    • A comparison of the photovoltaic response of head-to-head and head-to-tail coupled poly{(benzo-2,1,3-thiadiazol-4,7-diyl)-(dihexyl)[2, 2′]dithiophene-5,5′-diyl}
    • E. Bundgaard, and F.C. Kreb A comparison of the photovoltaic response of head-to-head and head-to-tail coupled poly{(benzo-2,1,3-thiadiazol-4,7-diyl)- (dihexyl)[2,2′]dithiophene-5,5′-diyl} Polym. Bull. 55 2005 157
    • (2005) Polym. Bull. , vol.55 , pp. 157
    • Bundgaard, E.1    Kreb, F.C.2
  • 23
    • 33744929653 scopus 로고    scopus 로고
    • Diarylethenes with intramolecular donor-acceptor structures for photo-induced electrochemical change
    • E. Kim, M. Kim, and K. Kim Diarylethenes with intramolecular donor-acceptor structures for photo-induced electrochemical change Tetrahedron 62 2006 6814
    • (2006) Tetrahedron , vol.62 , pp. 6814
    • Kim, E.1    Kim, M.2    Kim, K.3
  • 24
    • 36348956127 scopus 로고    scopus 로고
    • Synthesis, characterization, electrochemistry and optical properties of a novel phenanthrenequinone-alt-dialkylfluorene conjugated copolymer
    • M. Hanif, P. Lu, M. Li, Y. Zheng, Z. Xie, Y. Ma, and D. Li Synthesis, characterization, electrochemistry and optical properties of a novel phenanthrenequinone-alt-dialkylfluorene conjugated copolymer J. Polym. Int. 56 2007 1507
    • (2007) J. Polym. Int. , vol.56 , pp. 1507
    • Hanif, M.1    Lu, P.2    Li, M.3    Zheng, Y.4    Xie, Z.5    Ma, Y.6    Li, D.7
  • 25
    • 0037148430 scopus 로고    scopus 로고
    • Diastereoselective reaction of (MP)-pentahelicene-7,8-dione with trans-cyclohexane-1,2-diamine, thermal and photochemical transformations of its product
    • M. Putala, N.K. Pustet, and A. Mannschreck Diastereoselective reaction of (MP)-pentahelicene-7,8-dione with trans-cyclohexane-1,2-diamine, thermal and photochemical transformations of its product Tetrahedron Asymmetr. 12 2001 3333
    • (2001) Tetrahedron Asymmetr. , vol.12 , pp. 3333
    • Putala, M.1    Pustet, N.K.2    Mannschreck, A.3
  • 26
    • 42949140447 scopus 로고    scopus 로고
    • Facile synthesis of 9,10-diarylphenanthrenes and poly(9,10- diarylphenanthrenes)
    • B. He, H. Tian, Y. Geng, F. Wang, and K. Mullen Facile synthesis of 9,10-diarylphenanthrenes and poly(9,10-diarylphenanthrenes) Org. Lett. 10 2008 773
    • (2008) Org. Lett. , vol.10 , pp. 773
    • He, B.1    Tian, H.2    Geng, Y.3    Wang, F.4    Mullen, K.5
  • 27
    • 0014529834 scopus 로고
    • Iodination of fluorenone by N-iodosuccinimide
    • F. Dewhurst, and P. Shah Iodination of fluorenone by N-iodosuccinimide J. Chem. Soc. C 11 1969 1503
    • (1969) J. Chem. Soc. C , vol.11 , pp. 1503
    • Dewhurst, F.1    Shah, P.2
  • 28
    • 67149102416 scopus 로고    scopus 로고
    • Synthesis of electron-accepting polymers containing phenanthra-9,10- quinone units
    • J. Gautrot, P. Hodge, M. Helliwell, J. Raftery, and D. Cupertino Synthesis of electron-accepting polymers containing phenanthra-9,10-quinone units J. Mater. Chem. 19 2009 4148
    • (2009) J. Mater. Chem. , vol.19 , pp. 4148
    • Gautrot, J.1    Hodge, P.2    Helliwell, M.3    Raftery, J.4    Cupertino, D.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.