Issue 13, 2017

Aza boron-pyridyl-isoindoline analogues: synthesis and photophysical properties

Abstract

Several aza boron-pyridyl-isoindoline analogues are synthesized through a facile and scale-up two step reaction using 1,2-naphthalenedicarbonitrile as a starting material. These analogues show broad envelopes of intense vibrational bands in the absorption spectra with moderate fluorescence quantum yields in solution and the solid-state. An analysis of the structure–property relationships is described based on X-ray crystallography, optical spectroscopy, and theoretical calculations.

Graphical abstract: Aza boron-pyridyl-isoindoline analogues: synthesis and photophysical properties

Supplementary files

Article information

Article type
Paper
Submitted
01 Mar 2017
Accepted
30 May 2017
First published
31 May 2017

New J. Chem., 2017,41, 5802-5807

Aza boron-pyridyl-isoindoline analogues: synthesis and photophysical properties

H. Zhang, Y. Wu, M. Fan, X. Xiao, J. Mack, G. Kubheka, T. Nyokong and H. Lu, New J. Chem., 2017, 41, 5802 DOI: 10.1039/C7NJ00707H

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