메뉴 건너뛰기




Volumn 95, Issue 1, 2012, Pages 47-52

Synthesis and properties of triphenylamine-based hydrazones with reactive vinyl groups

Author keywords

Charge mobility; Hydrazone; Methoxy group; Polymerization; Triphenylamine; Vinyl group

Indexed keywords

CHARGE MOBILITIES; HYDRAZONES; METHOXY GROUP; TRIPHENYL AMINES; VINYL GROUP;

EID: 84859933987     PISSN: 01437208     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dyepig.2012.03.010     Document Type: Article
Times cited : (14)

References (29)
  • 1
    • 77953890426 scopus 로고    scopus 로고
    • Electroactive materials for organic electronics: Preparation strategies, structural aspects and characterization techniques
    • A. Pron, P. Gawrys, M. Zagorska, D. Djurado, and R. Demadrille Electroactive materials for organic electronics: preparation strategies, structural aspects and characterization techniques Chem Soc Rev 39 2010 2577 2632
    • (2010) Chem Soc Rev , vol.39 , pp. 2577-2632
    • Pron, A.1    Gawrys, P.2    Zagorska, M.3    Djurado, D.4    Demadrille, R.5
  • 2
    • 75649083797 scopus 로고    scopus 로고
    • Advances in organic photoconductor technology
    • D.S. Weiss, and M. Abkowitz Advances in organic photoconductor technology Chem Rev 110 2010 479 526
    • (2010) Chem Rev , vol.110 , pp. 479-526
    • Weiss, D.S.1    Abkowitz, M.2
  • 3
    • 77955395647 scopus 로고    scopus 로고
    • Molecular semiconductors in organic photovoltaic cells
    • A.W. Hains, Z. Liang, M.A. Woodhouse, and B. Gregg Molecular semiconductors in organic photovoltaic cells Chem Rev 110 2010 6689 6735
    • (2010) Chem Rev , vol.110 , pp. 6689-6735
    • Hains, A.W.1    Liang, Z.2    Woodhouse, M.A.3    Gregg, B.4
  • 4
    • 80555122816 scopus 로고    scopus 로고
    • Extended triphenylamine conjugated systems derivatized by perfluorophenyl groups
    • E. Ripaud, C. Mallet, M. Allain, P. Leriche, P. Frere, and J. Roncali Extended triphenylamine conjugated systems derivatized by perfluorophenyl groups Tetra Lett 52 2011 6573 6577
    • (2011) Tetra Lett , vol.52 , pp. 6573-6577
    • Ripaud, E.1    Mallet, C.2    Allain, M.3    Leriche, P.4    Frere, P.5    Roncali, J.6
  • 5
    • 67649390758 scopus 로고    scopus 로고
    • Poly(thiophenes) derivatized with oligo(oxyethylene) chains as donor materials for organic solar cells
    • Q. Bricaud, A. Cravino, P. Leriche, and J. Rancoli Poly(thiophenes) derivatized with oligo(oxyethylene) chains as donor materials for organic solar cells Sol Energy Mater Sol Cells 93 2009 1624 1629
    • (2009) Sol Energy Mater Sol Cells , vol.93 , pp. 1624-1629
    • Bricaud, Q.1    Cravino, A.2    Leriche, P.3    Rancoli, J.4
  • 10
    • 77649292948 scopus 로고    scopus 로고
    • A unimolecular half-subtractor based on effective photoinduced electron transfer and intramolecular charge transfer processes of 1,8-naphthalimide derivative
    • B. Leng, and H. Tian A unimolecular half-subtractor based on effective photoinduced electron transfer and intramolecular charge transfer processes of 1,8-naphthalimide derivative Austr J Chem 63 2010 169 172
    • (2010) Austr J Chem , vol.63 , pp. 169-172
    • Leng, B.1    Tian, H.2
  • 11
    • 79955386684 scopus 로고    scopus 로고
    • Dynamic random access memory devices based on functionalized copolymers with pendant hydrazine naphthalimide group
    • H. Li, N. Li, R. Sun, H. Gu, J. Ge, and J. Lu Dynamic random access memory devices based on functionalized copolymers with pendant hydrazine naphthalimide group J Phys Chem C 115 2011 8288 8294
    • (2011) J Phys Chem C , vol.115 , pp. 8288-8294
    • Li, H.1    Li, N.2    Sun, R.3    Gu, H.4    Ge, J.5    Lu, J.6
  • 12
    • 0033927513 scopus 로고    scopus 로고
    • Electroluminescence of organic materials
    • U. Mitschke, and P. Bauerle Electroluminescence of organic materials J Mater Chem 10 2000 1471 1507
    • (2000) J Mater Chem , vol.10 , pp. 1471-1507
    • Mitschke, U.1    Bauerle, P.2
  • 14
    • 33745966857 scopus 로고    scopus 로고
    • Modern trends in organic light-emitting devices (OLEDs)
    • DOI 10.1007/s00706-006-0490-4, Synthesis and Processing of Functional Polymers
    • O. Nuyken, S. Jungermann, V. Wiederhirn, E. Bacher, and K. Meerholz Modern trends in organic light-emitting devices (OLEDs) Monats Chem 137 2006 811 824 (Pubitemid 44060897)
    • (2006) Monatshefte fur Chemie , vol.137 , Issue.7 , pp. 811-824
    • Nuyken, O.1    Jungermann, S.2    Wiederhirn, V.3    Bacher, E.4    Meerholz, K.5
  • 15
    • 52349101423 scopus 로고    scopus 로고
    • Crosslinkable hole-transporting materials for solution processed polymer light-emitting diodes
    • F. Huang, Y.J. Cheng, Y. Zhang, M.S. Liu, and A.K.Y. Jen Crosslinkable hole-transporting materials for solution processed polymer light-emitting diodes J Mater Chem 18 2008 4495 4509
    • (2008) J Mater Chem , vol.18 , pp. 4495-4509
    • Huang, F.1    Cheng, Y.J.2    Zhang, Y.3    Liu, M.S.4    Jen, A.K.Y.5
  • 20
    • 0001211694 scopus 로고
    • Ionization potential of organic pigment film by atmospheric photoelectron emission analysis
    • E. Miyamoto, Y. Yamaguchi, and M. Yokoyama Ionization potential of organic pigment film by atmospheric photoelectron emission analysis Electrophotography 28 1989 364 370
    • (1989) Electrophotography , vol.28 , pp. 364-370
    • Miyamoto, E.1    Yamaguchi, Y.2    Yokoyama, M.3
  • 21
    • 0011180578 scopus 로고
    • Kinetics of photodischarge of negatively charged layers of Se
    • E. Montrimas, V. Gaidelis, and A. Pazera Kinetics of photodischarge of negatively charged layers of Se Lith J Phys 6 1966 569 573
    • (1966) Lith J Phys , vol.6 , pp. 569-573
    • Montrimas, E.1    Gaidelis, V.2    Pazera, A.3
  • 23
    • 80051583440 scopus 로고    scopus 로고
    • Structure-properties relationship of hydrazones containing methoxy-subsituted triphenylamino groups
    • V. Mimaite, J. Ostrauskaite, D. Gudeika, J.V. Grazulevicius, and V. Jankauskas structure-properties relationship of hydrazones containing methoxy-subsituted triphenylamino groups Snth Met 161 2011 1575 1581
    • (2011) Snth Met , vol.161 , pp. 1575-1581
    • Mimaite, V.1    Ostrauskaite, J.2    Gudeika, D.3    Grazulevicius, J.V.4    Jankauskas, V.5
  • 24
    • 23044467732 scopus 로고    scopus 로고
    • Practical and efficient synthesis of tris(4-formylphenyl)amine, a key building block in materials chemistry
    • DOI 10.1055/s-2005-865336, P01405SS
    • T. Mallegol, S. Gmouh, M.A.A. Mesiane, M. Blanchard-Desce, and O. Mongin Practical and efficient synthesis of tris(4-formylphenyl)amine, a key building block in materials chemistry Synthesis 11 2005 1771 1774 (Pubitemid 41058558)
    • (2005) Synthesis , Issue.11 , pp. 1771-1774
    • Mallegol, T.1    Gmouh, S.2    Meziane, M.A.A.3    Blanchard-Desce, M.4    Mongin, O.5
  • 26
    • 59849127195 scopus 로고    scopus 로고
    • Thermal polymerization of uninhibited styrene investigated by using microcalorimetry
    • C.C. Chen, Y.S. Duh, and C.M. Shu Thermal polymerization of uninhibited styrene investigated by using microcalorimetry J Hazard Mater 163 2009 1385 1390
    • (2009) J Hazard Mater , vol.163 , pp. 1385-1390
    • Chen, C.C.1    Duh, Y.S.2    Shu, C.M.3
  • 27
    • 52349101423 scopus 로고    scopus 로고
    • Crosslinkable hole-transporting materials for solution processed polymer light-emitting diodes
    • F. Huang, Y.J. Cheng, Y. Zahang, M.S. Liu, and A.K.Y. Jen Crosslinkable hole-transporting materials for solution processed polymer light-emitting diodes J Mat Chem 18 2008 4495 4509
    • (2008) J Mat Chem , vol.18 , pp. 4495-4509
    • Huang, F.1    Cheng, Y.J.2    Zahang, Y.3    Liu, M.S.4    Jen, A.K.Y.5
  • 28
    • 77949318400 scopus 로고    scopus 로고
    • Fumed silica-doped poly(butyl methacrylate-styrene)-based gel polymer electrolyte for lithium ion battery
    • Y.H. Liao, M.M. Rao, W.S. Li, L.T. Yang, B.K. Zhu, and R. Xu Fumed silica-doped poly(butyl methacrylate-styrene)-based gel polymer electrolyte for lithium ion battery J Membra Sci 352 2010 95 99
    • (2010) J Membra Sci , vol.352 , pp. 95-99
    • Liao, Y.H.1    Rao, M.M.2    Li, W.S.3    Yang, L.T.4    Zhu, B.K.5    Xu, R.6
  • 29
    • 0037466122 scopus 로고    scopus 로고
    • Stable free-radical polymerization of styrene in combination with 2-vinylnaphthalene initiation
    • J.R. Lizotte, and T.E. Long Stable free-radical polymerization of styrene in combination with 2-vinylnaphthalene initiation Macromol Chem Phys 204 2003 570 576
    • (2003) Macromol Chem Phys , vol.204 , pp. 570-576
    • Lizotte, J.R.1    Long, T.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.