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Volumn 13, Issue 7, 2012, Pages 1266-1276

Solution processable quinoxaline based molecular materials for organic field effect transistors

Author keywords

Charge transfer; D A D; Liquid crystal; Mobility; OFET; Quinoxaline

Indexed keywords

CARRIER MOBILITY; CHARGE TRANSFER; CYCLIC VOLTAMMETRY; DIFFERENTIAL SCANNING CALORIMETRY; ELECTRONIC STRUCTURE; GRAVIMETRIC ANALYSIS; LIQUID CRYSTALS; MOLECULES; ORGANIC FIELD EFFECT TRANSISTORS; THERMOGRAVIMETRIC ANALYSIS; ULTRAVIOLET VISIBLE SPECTROSCOPY; X RAY DIFFRACTION;

EID: 84860306731     PISSN: 15661199     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.orgel.2012.03.012     Document Type: Article
Times cited : (15)

References (49)
  • 4
    • 0000053544 scopus 로고    scopus 로고
    • Conjugated polymer-based chemical sensors
    • D.T. McQuade, A.E. Pullen, and T.M. Swager Conjugated polymer-based chemical sensors Chem. Rev. 100 2000 2537 2574
    • (2000) Chem. Rev. , vol.100 , pp. 2537-2574
    • McQuade, D.T.1    Pullen, A.E.2    Swager, T.M.3
  • 5
    • 77951646183 scopus 로고    scopus 로고
    • Functionalized polypyrrole film: Synthesis, characterization, and potential applications in chemical and biological sensors
    • H. Dong, X. Cao, and C.M. Li Functionalized polypyrrole film: synthesis, characterization, and potential applications in chemical and biological sensors ACS Appl. Mater. Interfaces 1 2009 1599 1606
    • (2009) ACS Appl. Mater. Interfaces , vol.1 , pp. 1599-1606
    • Dong, H.1    Cao, X.2    Li, C.M.3
  • 6
    • 78650355746 scopus 로고    scopus 로고
    • Recent progress on polymer-based fluorescent and colorimetric chemosensors
    • H.N. Kim, Z. Guo, W. Zhu, J. Yoon, and H. Tian Recent progress on polymer-based fluorescent and colorimetric chemosensors Chem. Soc. Rev. 40 2011 79 93
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 79-93
    • Kim, H.N.1    Guo, Z.2    Zhu, W.3    Yoon, J.4    Tian, H.5
  • 7
    • 79951793339 scopus 로고    scopus 로고
    • Organic semiconductor memory devices based on a low-band gap polyfluorene derivative with isoindigo as electron-trapping moieties
    • X. Xu, L. Li, B. Liu, and Y. Zou Organic semiconductor memory devices based on a low-band gap polyfluorene derivative with isoindigo as electron-trapping moieties Appl. Phys. Lett. 98 2011 063303
    • (2011) Appl. Phys. Lett. , vol.98 , pp. 063303
    • Xu, X.1    Li, L.2    Liu, B.3    Zou, Y.4
  • 11
    • 0032869272 scopus 로고    scopus 로고
    • Printable organic and polymeric semiconducting materials and devices
    • Z. Bao, J.A. Rogers, and H.E. Katz Printable organic and polymeric semiconducting materials and devices J. Mater. Chem. 9 1999 1895 1904
    • (1999) J. Mater. Chem. , vol.9 , pp. 1895-1904
    • Bao, Z.1    Rogers, J.A.2    Katz, H.E.3
  • 14
    • 77956962806 scopus 로고    scopus 로고
    • Organic transistors in optical displays and microelectronic applications
    • G. Gelinck, P. Heremans, K. Nomoto, and T.D. Anthopoulos Organic transistors in optical displays and microelectronic applications Adv. Mater. 22 2010 3778 3798
    • (2010) Adv. Mater. , vol.22 , pp. 3778-3798
    • Gelinck, G.1    Heremans, P.2    Nomoto, K.3    Anthopoulos, T.D.4
  • 15
    • 77957685551 scopus 로고    scopus 로고
    • Product integration of compact roll-to-roll processed polymer solar cell modules: Methods and manufacture using flexographic printing, slot-die coating and rotary screen printing
    • F.C. Krebs, J. Fyenbo, and M. Jorgensen Product integration of compact roll-to-roll processed polymer solar cell modules: methods and manufacture using flexographic printing, slot-die coating and rotary screen printing J. Mater. Chem. 20 2010 8994 9001
    • (2010) J. Mater. Chem. , vol.20 , pp. 8994-9001
    • Krebs, F.C.1    Fyenbo, J.2    Jorgensen, M.3
  • 16
    • 8544256330 scopus 로고    scopus 로고
    • Thin film deposition, patterning, and printing in organic thin film transistors
    • M.M. Ling, and Z. Bao Thin film deposition, patterning, and printing in organic thin film transistors Chem. Mater. 16 2004 4824 4840
    • (2004) Chem. Mater. , vol.16 , pp. 4824-4840
    • Ling, M.M.1    Bao, Z.2
  • 18
    • 20444458036 scopus 로고    scopus 로고
    • Ink-jet printing, self-assembled polyelectrolytes, and electroless plating: Low cost fabrication of circuits on a flexible substrate at room temperature
    • K. Cheng, M.-H. Yang, W.W.W. Chiu, C.-Y. Huang, J. Chang, T.-F. Ying, and Y. Yang Ink-jet printing, self-assembled polyelectrolytes, and electroless plating: low cost fabrication of circuits on a flexible substrate at room temperature Macromol. Rapid Commun. 26 2005 247 264
    • (2005) Macromol. Rapid Commun. , vol.26 , pp. 247-264
    • Cheng, K.1    Yang, M.-H.2    Chiu, W.W.W.3    Huang, C.-Y.4    Chang, J.5    Ying, T.-F.6    Yang, Y.7
  • 19
    • 34547169908 scopus 로고    scopus 로고
    • Rubrene polycrystalline transistor channel achieved through in situ vacuum annealing
    • S.W. Park, S. Jeong, J.M. Choi, J.M. Hwang, J.H. Kim, and S. Im Rubrene polycrystalline transistor channel achieved through in situ vacuum annealing Appl. Phys. Lett. 91 2007 033506
    • (2007) Appl. Phys. Lett. , vol.91 , pp. 033506
    • Park, S.W.1    Jeong, S.2    Choi, J.M.3    Hwang, J.M.4    Kim, J.H.5    Im, S.6
  • 20
    • 53549093322 scopus 로고    scopus 로고
    • Organic semiconductors for solution-processable field-effect transistors (OFETs)
    • S. Allard, M. Forster, B. Souharce, H. Thiem, and U. Scherf Organic semiconductors for solution-processable field-effect transistors (OFETs) Angew. Chem. Int. Ed. 47 2008 4070 4098
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4070-4098
    • Allard, S.1    Forster, M.2    Souharce, B.3    Thiem, H.4    Scherf, U.5
  • 23
    • 75749132800 scopus 로고    scopus 로고
    • Materials and applications for large area electronics: Solution-based approaches
    • A.C. Arias, J.D. MacKenzie, I. McCulloch, J. Rivnay, and A. Salleo Materials and applications for large area electronics: solution-based approaches Chem. Rev. 110 2010 3 24
    • (2010) Chem. Rev. , vol.110 , pp. 3-24
    • Arias, A.C.1    MacKenzie, J.D.2    McCulloch, I.3    Rivnay, J.4    Salleo, A.5
  • 24
    • 33846219497 scopus 로고    scopus 로고
    • Functionalized acenes and heteroacenes for organic electronics
    • J.E. Anthony Functionalized acenes and heteroacenes for organic electronics Chem. Rev. 106 2006 5028 5048
    • (2006) Chem. Rev. , vol.106 , pp. 5028-5048
    • Anthony, J.E.1
  • 26
    • 0042709503 scopus 로고    scopus 로고
    • Easily processable phenylene-thiophene-based organic field-effect transistors and solution-fabricated nonvolatile transistor memory elements
    • M. Mushrush, A. Facchetti, M. Lefenfeld, H.E. Katz, and T.J. Marks Easily processable phenylene-thiophene-based organic field-effect transistors and solution-fabricated nonvolatile transistor memory elements J. Am. Chem. Soc. 125 2003 9414 9423
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 9414-9423
    • Mushrush, M.1    Facchetti, A.2    Lefenfeld, M.3    Katz, H.E.4    Marks, T.J.5
  • 27
    • 66149112877 scopus 로고    scopus 로고
    • High electron mobility and ambient stability in solution-processed perylene-based organic field-effect transistors
    • C. Piliego, D. Jarzab, G. Gigli, Z. Chen, A. Facchetti, and M.A. Loi High electron mobility and ambient stability in solution-processed perylene-based organic field-effect transistors Adv. Mater. 21 2009 1573 1576
    • (2009) Adv. Mater. , vol.21 , pp. 1573-1576
    • Piliego, C.1    Jarzab, D.2    Gigli, G.3    Chen, Z.4    Facchetti, A.5    Loi, M.A.6
  • 28
    • 0346937202 scopus 로고    scopus 로고
    • Functionalized pentacene active layer organic thin-film transistors
    • C.D. Sheraw, T.N. Jackson, D.L. Eaton, and J.E. Anthony Functionalized pentacene active layer organic thin-film transistors Adv. Mater. 15 2003 2009 2011
    • (2003) Adv. Mater. , vol.15 , pp. 2009-2011
    • Sheraw, C.D.1    Jackson, T.N.2    Eaton, D.L.3    Anthony, J.E.4
  • 31
    • 0001090687 scopus 로고    scopus 로고
    • Mobility enhancement in conjugated polymer field-effect transistors through chain alignment in a liquid-crystalline phase
    • H. Sirringhaus, R. Wilson, R. Friend, M. Inbasekaran, W. Wu, E. Woo, M. Grell, and D. Bradley Mobility enhancement in conjugated polymer field-effect transistors through chain alignment in a liquid-crystalline phase Appl. Phys. Lett. 77 2000 406
    • (2000) Appl. Phys. Lett. , vol.77 , pp. 406
    • Sirringhaus, H.1    Wilson, R.2    Friend, R.3    Inbasekaran, M.4    Wu, W.5    Woo, E.6    Grell, M.7    Bradley, D.8
  • 32
    • 60149093091 scopus 로고    scopus 로고
    • π-Conjugated Oligothiophene-based polycatenar liquid crystals: Self-organization and photoconductive, luminescent, and redox properties
    • T. Yasuda, H. Ooi, J. Morita, Y. Akama, K. Minoura, M. Funahashi, T. Shimomura, and T. Kato π-Conjugated Oligothiophene-based polycatenar liquid crystals: self-organization and photoconductive, luminescent, and redox properties Adv. Funct. Mater. 19 2009 411 419
    • (2009) Adv. Funct. Mater. , vol.19 , pp. 411-419
    • Yasuda, T.1    Ooi, H.2    Morita, J.3    Akama, Y.4    Minoura, K.5    Funahashi, M.6    Shimomura, T.7    Kato, T.8
  • 33
    • 79954485045 scopus 로고    scopus 로고
    • Availability of liquid crystallinity in solution processing for polycrystalline thin Films
    • H. Iino, and J.-I. Hanna Availability of liquid crystallinity in solution processing for polycrystalline thin Films Adv. Mater. 23 2011 1748 1751
    • (2011) Adv. Mater. , vol.23 , pp. 1748-1751
    • Iino, H.1    Hanna, J.-I.2
  • 34
  • 35
    • 0001518311 scopus 로고    scopus 로고
    • Fast hole transport in a new calamitic liquid crystal of 2-(4′-heptyloxyphenyl)-6-dodecylthiobenzothiazole
    • M. Funahashi, and J.-i. Hanna Fast hole transport in a new calamitic liquid crystal of 2-(4′-heptyloxyphenyl)-6-dodecylthiobenzothiazole Phys. Rev. Lett. 78 1997 2184
    • (1997) Phys. Rev. Lett. , vol.78 , pp. 2184
    • Funahashi, M.1    H, J.-I.2
  • 36
    • 34250358182 scopus 로고    scopus 로고
    • High ambipolar mobility in a highly ordered smectic phase of a dialkylphenylterthiophene derivative that can be applied to solution-processed organic field-effect transistors
    • M. Funahashi, F. Zhang, and N. Tamaoki High ambipolar mobility in a highly ordered smectic phase of a dialkylphenylterthiophene derivative that can be applied to solution-processed organic field-effect transistors Adv. Mater. 19 2007 353 358
    • (2007) Adv. Mater. , vol.19 , pp. 353-358
    • Funahashi, M.1    Zhang, F.2    Tamaoki, N.3
  • 38
    • 16244379589 scopus 로고    scopus 로고
    • -1 at ambient temperatures in thiophene-based smectic liquid crystals
    • -1 at ambient temperatures in thiophene-based smectic liquid crystals Adv. Mater. 17 2005 594 598
    • (2005) Adv. Mater. , vol.17 , pp. 594-598
    • Funahashi, M.1    Hanna, J.I.2
  • 39
    • 0033517645 scopus 로고    scopus 로고
    • Electroluminescence and photophysical properties of polyquinolines
    • X. Zhang, A.S. Shetty, and S.A. Jenekhe Electroluminescence and photophysical properties of polyquinolines Macromolecules 32 1999 7422 7429
    • (1999) Macromolecules , vol.32 , pp. 7422-7429
    • Zhang, X.1    Shetty, A.S.2    Jenekhe, S.A.3
  • 40
    • 84863115773 scopus 로고    scopus 로고
    • Tuning the photovoltaic parameters of thiophene-linked donor-acceptor liquid crystalline copolymers for organic photovoltaics
    • K. Yao, L. Chen, Y. Chen, F. Li, X. Ren, H. Wang, and Y. Li Tuning the photovoltaic parameters of thiophene-linked donor-acceptor liquid crystalline copolymers for organic photovoltaics Polym. Chem. 3 2012
    • (2012) Polym. Chem. , vol.3
    • Yao, K.1    Chen, L.2    Chen, Y.3    Li, F.4    Ren, X.5    Wang, H.6    Li, Y.7
  • 42
    • 20444383861 scopus 로고    scopus 로고
    • New alternative donor-acceptor arranged poly(aryleneethynylene)s and their related compounds composed of five-membered electron-accepting 1,3,4-thiadiazole, 1,2,4-triazole, or 3,4-dinitrothiophene units: Synthesis, packing structure, and optical properties
    • T. Yasuda, T. Imase, Y. Nakamura, and T. Yamamoto New alternative donor-acceptor arranged poly(aryleneethynylene)s and their related compounds composed of five-membered electron-accepting 1,3,4-thiadiazole, 1,2,4-triazole, or 3,4-dinitrothiophene units: synthesis, packing structure, and optical properties Macromolecules 38 2005 4687 4697
    • (2005) Macromolecules , vol.38 , pp. 4687-4697
    • Yasuda, T.1    Imase, T.2    Nakamura, Y.3    Yamamoto, T.4
  • 43
    • 10244229148 scopus 로고    scopus 로고
    • Charge-transfer and energy-transfer processes in π-conjugated oligomers and polymers: A molecular picture
    • J.-L. Brédas, D. Beljonne, V. Coropceanu, and J. Cornil Charge-transfer and energy-transfer processes in π-conjugated oligomers and polymers: a molecular picture Chem. Rev. 104 2004 4971 5004
    • (2004) Chem. Rev. , vol.104 , pp. 4971-5004
    • Brédas, J.-L.1    Beljonne, D.2    Coropceanu, V.3    Cornil, J.4
  • 45
    • 34547961146 scopus 로고    scopus 로고
    • Derivatives of 4,9-dihydro-s-indaceno[1,2-b:5,6-b′]dithiophene-4,9- dione: Synthesis and properties
    • C. Zhao, Y. Zhang, and M.-K. Ng Derivatives of 4,9-dihydro-s-indaceno[1, 2-b:5,6-b′]dithiophene-4,9-dione: synthesis and properties J. Org. Chem. 72 2007 6364 6371
    • (2007) J. Org. Chem. , vol.72 , pp. 6364-6371
    • Zhao, C.1    Zhang, Y.2    Ng, M.-K.3
  • 46
    • 33746871766 scopus 로고    scopus 로고
    • Ring fusion effects on the solid-state properties of - Oligothiophenes
    • X. Zhang, J.P. Johnson, J.W. Kampf, and A.J. Matzger Ring fusion effects on the solid-state properties of - oligothiophenes Chem. Mat. 18 2006 3470 3476
    • (2006) Chem. Mat. , vol.18 , pp. 3470-3476
    • Zhang, X.1    Johnson, J.P.2    Kampf, J.W.3    Matzger, A.J.4
  • 47
    • 0037459306 scopus 로고    scopus 로고
    • Steady-state and time-resolved studies of 2,7-carbazole-based conjugated polymers in solution and as thin films: Determination of their solid state fluorescence quantum efficiencies
    • S. Tirapattur, M. Belletête, N. Drolet, M. Leclerc, and G. Durocher Steady-state and time-resolved studies of 2,7-carbazole-based conjugated polymers in solution and as thin films: determination of their solid state fluorescence quantum efficiencies Chem. Phys. Lett. 370 2003 799 804
    • (2003) Chem. Phys. Lett. , vol.370 , pp. 799-804
    • Tirapattur, S.1    Belletête, M.2    Drolet, N.3    Leclerc, M.4    Durocher, G.5
  • 49
    • 77955352849 scopus 로고    scopus 로고
    • High quality shadow masks for top contact organic field effect transistors using deep reactive ion etching
    • M. Aljada, K. Mutkins, G. Vamvounis, P. Burn, and P. Meredith High quality shadow masks for top contact organic field effect transistors using deep reactive ion etching J. Micromech. Microeng. 20 2010 075037
    • (2010) J. Micromech. Microeng. , vol.20 , pp. 075037
    • Aljada, M.1    Mutkins, K.2    Vamvounis, G.3    Burn, P.4    Meredith, P.5


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