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Issue 49, 2017
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Naphtho[b]-fused BODIPYs: one pot Suzuki–Miyaura–Knoevenagel synthesis and photophysical properties

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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.

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

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Article information


Submitted
16 Apr 2017
Accepted
25 May 2017
First published
25 May 2017

Chem. Commun., 2017,53, 6621-6624
Article type
Communication

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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