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Volumn , Issue 41, 2008, Pages 5170-5172

Defect chemistry of polyfluorenes: Identification of the origin of "interface defects" in polyfluorene based light-emitting devices

Author keywords

[No Author keywords available]

Indexed keywords

FLUORENE DERIVATIVE; HYDROXYL GROUP; POLYMER;

EID: 54949123065     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b808407f     Document Type: Article
Times cited : (31)

References (26)
  • 2
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    • Synthetic Methods for Semiconducting Polymers, in
    • G. Hadziioannou and G. G. Malliaras, Wiley-VCH, Weinheim
    • A. Bolognesi and M. C. Pasini, Synthetic Methods for Semiconducting Polymers, in Semiconducting Polymers, ed., G. Hadziioannou, and, G. G. Malliaras,, Wiley-VCH, Weinheim, 2007
    • (2007) Semiconducting Polymers, Ed.
    • Bolognesi, A.1    Pasini, M.C.2
  • 20
    • 84889331460 scopus 로고    scopus 로고
    • The Synthesis of Electroluminescent Polymers, in
    • K. Müllen and U. Scherf, Wiley-VCH, Weinheim
    • A. C. Grimsdale, The Synthesis of Electroluminescent Polymers, in Organic Light-Emitting Devices, ed., K. Müllen, and, U. Scherf,, Wiley-VCH, Weinheim, 2006
    • (2006) Organic Light-Emitting Devices, Ed.
    • Grimsdale, A.C.1
  • 21
    • 20544450502 scopus 로고    scopus 로고
    • Mechanistic Aspects of Metal-Catalyzed C,C- and C,X-Bond-Forming Reactions, in
    • A. De Meijere and F. Diederich, Wiley-VCH, Weinheim
    • A. M. Echavarren and D. J. Cardenas, Mechanistic Aspects of Metal-Catalyzed C,C- and C,X-Bond-Forming Reactions, in Metal-Catalyzed Cross-Coupling Reactions, ed., A. De Meijere, and, F. Diederich,, Wiley-VCH, Weinheim, 2004
    • (2004) Metal-Catalyzed Cross-Coupling Reactions, Ed.
    • Echavarren, A.M.1    Cardenas, D.J.2
  • 23
    • 34248169307 scopus 로고    scopus 로고
    • It should be noted that attempts to prepare thin films from 2 and 3 were unsuccessful due to very poor film forming properties The weak residual blue emission of 1 upon deprotonation can be rationalized by polyfluorene chains bearing no hydroxy end groups
    • M. Zelzer S. Kappaun E. Zojer C. Slugovc Monatsh. Chem. 2007 138 453
    • (2007) Monatsh. Chem. , vol.138 , pp. 453
    • Zelzer, M.1    Kappaun, S.2    Zojer, E.3    Slugovc, C.4
  • 24
    • 54949148316 scopus 로고    scopus 로고
    • Because of these reprotonation effects attempts to determine the quantum yields of the deprotonated species were unsuccessful
    • Because of these reprotonation effects attempts to determine the quantum yields of the deprotonated species were unsuccessful


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