Issue 57, 2016, Issue in Progress
From the journal:

RSC Advances

Synthesis, structure and photophysical properties of near-infrared 3,5-diarylbenzoBODIPY fluorophores†

Jun Wang,a   Qinghua Wu,a   Yajun Xu,a   Changjiang Yu,a   Yun Wei,a   Xiaolong Mu,a   Erhong Hao*a  and  Lijuan Jiao*a  

* Corresponding authors

a The Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Laboratory of Molecule-Based Materials, School of Chemistry and Materials Science, Anhui Normal University, Wuhu, China
E-mail: haoehong@ahnu.edu.cn, jiao421@ahnu.edu.cn

Abstract

A set of 3,5-diarylated benzoBODIPYs were prepared within three steps from commercial isoindolin-1-one via Vilsmeier Haack, Suzuki coupling and a one-pot POCl3-promoted self-condensation in concert with a BF3 complexation. These benzoBODIPYs showed strong absorption and intense fluorescence emission in far-red to NIR region (λmaxabs = 634–706 nm, λmaxem = 663–747 nm, Φ = 0.35–0.99) tunable via the variation of the 3,5-aryl substituents.

Graphical abstract: Synthesis, structure and photophysical properties of near-infrared 3,5-diarylbenzoBODIPY fluorophores

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Article information

DOI
https://doi.org/10.1039/C6RA04412C
Article type
Paper
Submitted
18 Feb 2016
Accepted
20 May 2016
First published
23 May 2016

RSC Adv., 2016,6, 52180-52188

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Synthesis, structure and photophysical properties of near-infrared 3,5-diarylbenzoBODIPY fluorophores

J. Wang, Q. Wu, Y. Xu, C. Yu, Y. Wei, X. Mu, E. Hao and L. Jiao, RSC Adv., 2016, 6, 52180 DOI: 10.1039/C6RA04412C

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