Functionalization of BODIPY dyes at 2,6-positions through formyl groups
Document Type
Article
Publication Date
4-14-2013
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. © 2012 The Royal Society of Chemistry.
Publication Title
RSC Advances
Recommended Citation
Zhu, S.,
Bi, J.,
Vegesna, G.,
Zhang, J.,
Luo, F.,
Valenzano, L.,
&
Liu, H.
(2013).
Functionalization of BODIPY dyes at 2,6-positions through formyl groups.
RSC Advances,
3(14), 4793-4800.
http://doi.org/10.1039/c3ra22610g
Retrieved from: https://digitalcommons.mtu.edu/michigantech-p/8511