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Embedding a boroxazine ring into a nanographene scaffold by a concise bottom-up synthetic strategy

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Abstract

Embedding a boroxazine (B3N2O) heterocycle by a m-quinquephenyl scaffold renders a B/N/O substituted nanographene molecule. The target compound can be synthesized in four steps and in good overall yield. The incorporation of a boroxazine core modifies the electronic structure and results in high fluorescence quantum yield.

Graphical abstract: Embedding a boroxazine ring into a nanographene scaffold by a concise bottom-up synthetic strategy

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Article information


Submitted
17 Jan 2020
Accepted
06 Feb 2020
First published
24 Feb 2020

Chem. Commun., 2020, Advance Article
Article type
Communication

Embedding a boroxazine ring into a nanographene scaffold by a concise bottom-up synthetic strategy

M. Fingerle and H. F. Bettinger, Chem. Commun., 2020, Advance Article , DOI: 10.1039/D0CC00471E

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