Issue 14, 2013
From the journal:

RSC Advances

Functionalization of BODIPY dyes at 2,6-positions through formyl groups†

Shilei Zhu,*a   Jianheng Bi,a   Giri Vegesna,a   Jingtuo Zhang,a   Fen-Tair Luo,*b   Loredana Valenzano*a  and  Haiying Liu*a  

* Corresponding authors

a Department of Chemistry, Michigan Technological University, 1400 Townsend Drive, Houghton, Michigan 49931-1295, USA
E-mail: shileiz@mtu.edu, lvalenza@mtu.edu, hyliu@mtu.edu
Fax: (+)01-906-487-2061

b Institute of Chemistry, Academia Sinica, Taipei, Taiwan 11529, Republic of China
E-mail: luoft@gate.sinica.deu.tw

Abstract

A 2,6-diformyl-BODIPY dye has been modified by transforming its formyl groups at the 2,6-positions into different functional groups such as hydroxyl, carboxylic acid, cyano, nitro and oxime groups, resulting in a series of new BODIPY dyes. The optical properties of the resulting BODIPY dyes significantly depend on the functional groups at the 2,6-positions.

Graphical abstract: Functionalization of BODIPY dyes at 2,6-positions through formyl groups

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Article information

DOI
https://doi.org/10.1039/C3RA22610G
Article type
Paper
Submitted
24 Oct 2012
Accepted
24 Jan 2013
First published
28 Jan 2013

RSC Adv., 2013,3, 4793-4800

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Functionalization of BODIPY dyes at 2,6-positions through formyl groups

S. Zhu, J. Bi, G. Vegesna, J. Zhang, F. Luo, L. Valenzano and H. Liu, RSC Adv., 2013, 3, 4793 DOI: 10.1039/C3RA22610G

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