Issue 49, 2017

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

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

Supplementary files

Article information

Article type
Communication
Submitted
16 Apr 2017
Accepted
25 May 2017
First published
25 May 2017

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

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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