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Issue 13, 2017
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Aza boron-pyridyl-isoindoline analogues: synthesis and photophysical properties

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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

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Publication details

The article was received on 01 Mar 2017, accepted on 30 May 2017 and first published on 31 May 2017


Article type: Paper
DOI: 10.1039/C7NJ00707H
Citation: New J. Chem., 2017,41, 5802-5807
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    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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