Naphtho[b]-fused BODIPYs: one pot Suzuki–Miyaura–Knoevenagel synthesis and photophysical properties

Zhikuan Zhou; Jianping Zhou; Lizhi Gai; Aihua Yuan; Zhen Shen

doi:10.1039/C7CC02918G

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Naphtho[b]-fused BODIPYs: one pot Suzuki–Miyaura–Knoevenagel synthesis and photophysical properties†

Zhikuan Zhou,

*^ab Jianping Zhou,^a Lizhi Gai,^b Aihua Yuan

*^a and Zhen Shen*^b

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* Corresponding authors

^a School of Environmental and Chemical Engineering, Jiangsu University of Science and Technology, Zhenjiang 212003, P. R. China
E-mail: zkzhou@just.edu.cn, aihua.yuan@just.edu.cn
Fax: +86-511-85635850
Tel: +86-511-85639001

^b State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, P. R. China
E-mail: zshen@nju.edu.cn

Abstract

Naphtho[b]-fused BODIPYs have been facilely synthesized via Suzuki–Miyaura–Knoevenagel reaction between mono-iodo-BODIPY or 2,6-diiodo-BODIPY with (2-formylphenyl)boronic acid. This one-pot reaction represents a very straightforward approach for tuning the absorption and emission of BODIPYs in the red visible/NIR range.

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DOI: https://doi.org/10.1039/C7CC02918G
Article type: Communication
Submitted: 16 Apr 2017
Accepted: 25 May 2017
First published: 25 May 2017

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Chem. Commun., 2017,53, 6621-6624

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Naphtho[b]-fused BODIPYs: one pot Suzuki–Miyaura–Knoevenagel synthesis and photophysical properties

Z. Zhou, J. Zhou, L. Gai, A. Yuan and Z. Shen, Chem. Commun., 2017, 53, 6621 DOI: 10.1039/C7CC02918G

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Chemical Communications

Naphtho[b]-fused BODIPYs: one pot Suzuki–Miyaura–Knoevenagel synthesis and photophysical properties†

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Naphtho[b]-fused BODIPYs: one pot Suzuki–Miyaura–Knoevenagel synthesis and photophysical properties

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