Issue 10, 2017

Enhancing field-effect mobility and maintaining solid-state emission by incorporating 2,6-diphenyl substitution to 9,10-bis(phenylethynyl)anthracene

Abstract

The development of optical and electrical organic semiconductors is crucial for the construction of integrated optoelectronic devices. Herein, a new anthracene derivative, 2,6-diphenyl-9,10-bis(phenylethynyl)anthracene (DP-BPEA), was designed and synthesized by enlarging the π-conjugation of 9,10-bis(phenylethynyl)anthracene (BPEA) via 2,6-diphenyl substitution. Compared with the parent BPEA molecule, an improved field-effect mobility of 1.37 cm2 V−1 s−1 with a comparable solid fluorescence efficiency of 32% is obtained for DP-BPEA, suggesting its potential applications in integrated optoelectronic devices.

Graphical abstract: Enhancing field-effect mobility and maintaining solid-state emission by incorporating 2,6-diphenyl substitution to 9,10-bis(phenylethynyl)anthracene

Supplementary files

Article information

Article type
Communication
Submitted
22 jan 2017
Accepted
18 feb 2017
First published
20 feb 2017

J. Mater. Chem. C, 2017,5, 2519-2523

Enhancing field-effect mobility and maintaining solid-state emission by incorporating 2,6-diphenyl substitution to 9,10-bis(phenylethynyl)anthracene

J. Liu, J. Liu, Z. Zhang, C. Xu, Q. Li, K. Zhou, H. Dong, X. Zhang and W. Hu, J. Mater. Chem. C, 2017, 5, 2519 DOI: 10.1039/C7TC00372B

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