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Issue 18, 2018
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Eaton's reagent assisted aromatic C–C coupling of carbazoles for optoelectronic applications

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Abstract

An Eaton's reagent assisted C(sp2)–C(sp2) coupling via the Scholl reaction mechanism was developed to prepare bicarbazoles without using any solvents and catalysts. The resulting biaryl exhibits unique optoelectronic properties as a promising host material of blue phosphorescent organic light emitting diodes, achieving high current efficiency up to 31.7 cd A−1 with ultralow roll-off.

Graphical abstract: Eaton's reagent assisted aromatic C–C coupling of carbazoles for optoelectronic applications

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Publication details

The article was received on 02 Jul 2018, accepted on 30 Jul 2018 and first published on 03 Aug 2018


Article type: Letter
DOI: 10.1039/C8NJ03296C
Citation: New J. Chem., 2018,42, 14704-14708
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    Eaton's reagent assisted aromatic C–C coupling of carbazoles for optoelectronic applications

    J. Yuan, L. Jin, R. Chen, X. Tang, X. Xie, Y. Tang and W. Huang, New J. Chem., 2018, 42, 14704
    DOI: 10.1039/C8NJ03296C

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