Issue 2, 2012

Controlled Knoevenagel reactions of methyl groups of 1,3,5,7-tetramethyl BODIPY dyes for unique BODIPY dyes

Abstract

Formyl groups at 6- and 2,6-positions initiated Knoevenagel reactions of the methyl groups at the 7, and 1,7-positions of 1,3,5,7-tetramethyl BODIPY dyes with aromatic aldehydes. Formation of vinyl bonds at the 7-, and 1,7-positions facilitates further Knoevenagel reactions of the methyl groups at the 3,5-positions. This approach offers fast, facile and versatile ways to prepare potential novel building blocks of BODIPY dyes for conjugated oligomers, dendrimers, and highly water-soluble, near-infrared emissive sensing materials.

Graphical abstract: Controlled Knoevenagel reactions of methyl groups of 1,3,5,7-tetramethyl BODIPY dyes for unique BODIPY dyes

Supplementary files

Article information

Article type
Communication
Submitted
05 set 2011
Accepted
10 out 2011
First published
04 nov 2011

RSC Adv., 2012,2, 404-407

Controlled Knoevenagel reactions of methyl groups of 1,3,5,7-tetramethyl BODIPY dyes for unique BODIPY dyes

S. Zhu, J. Zhang, G. Vegesna, A. Tiwari, F. Luo, M. Zeller, R. Luck, H. Li, S. Green and H. Liu, RSC Adv., 2012, 2, 404 DOI: 10.1039/C1RA00678A

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