Issue 93, 2014

Construction of fluorescence-tunable pyrido-fused benzimidazoles via direct intramolecular C–H amination under transition-metal-free conditions

Abstract

A novel methodology was discovered to construct multi-phenyl substituted pyrido-fused benzimidazole (PBI) core frameworks via direct oxidative intramolecular C–H amination of α-unsubstituted pyridinium salts under transition-metal free conditions. The resulting highly π-conjugated PBI derivatives exhibited highly tunable fluorescent emission not only in solution but also in the solid state.

Graphical abstract: Construction of fluorescence-tunable pyrido-fused benzimidazoles via direct intramolecular C–H amination under transition-metal-free conditions

Supplementary files

Article information

Article type
Communication
Submitted
20 Aug 2014
Accepted
07 Oct 2014
First published
08 Oct 2014

RSC Adv., 2014,4, 51268-51271

Author version available

Construction of fluorescence-tunable pyrido-fused benzimidazoles via direct intramolecular C–H amination under transition-metal-free conditions

W. Gong, P. Gao, G. Li, H. Mehdi, G. Ning and J. Yu, RSC Adv., 2014, 4, 51268 DOI: 10.1039/C4RA08954E

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