Eaton's reagent assisted aromatic C-C coupling of carbazoles for optoelectronic applications

Jie Yuan; Lu Jin; Runfeng Chen; Xingxing Tang; Xiang Xie; Yuting Tang; Wei Huang

doi:10.1039/c8nj03296c

Eaton's reagent assisted aromatic C-C coupling of carbazoles for optoelectronic applications

Jie Yuan, Lu Jin, Runfeng Chen, Xingxing Tang, Xiang Xie, Yuting Tang, Wei Huang

Nanjing University of Posts and Telecommunications

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

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.

Original language	English
Pages (from-to)	14704-14708
Number of pages	5
Journal	New Journal of Chemistry
Volume	42
Issue number	18
DOIs	https://doi.org/10.1039/c8nj03296c
State	Published - 2018
Externally published	Yes

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title = "Eaton's reagent assisted aromatic C-C coupling of carbazoles for optoelectronic applications",

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.",

author = "Jie Yuan and Lu Jin and Runfeng Chen and Xingxing Tang and Xiang Xie and Yuting Tang and Wei Huang",

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T1 - Eaton's reagent assisted aromatic C-C coupling of carbazoles for optoelectronic applications

AU - Yuan, Jie

AU - Jin, Lu

AU - Chen, Runfeng

AU - Tang, Xingxing

AU - Xie, Xiang

AU - Tang, Yuting

AU - Huang, Wei

N1 - Publisher Copyright: This journal is © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.

PY - 2018

Y1 - 2018

N2 - 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.

AB - 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.

UR - https://www.scopus.com/pages/publications/85053717060

U2 - 10.1039/c8nj03296c

DO - 10.1039/c8nj03296c

M3 - 文章

AN - SCOPUS:85053717060

SN - 1144-0546

VL - 42

SP - 14704

EP - 14708

JO - New Journal of Chemistry

JF - New Journal of Chemistry

IS - 18

ER -

Eaton's reagent assisted aromatic C-C coupling of carbazoles for optoelectronic applications

Abstract

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