877616-05-2Relevant academic research and scientific papers
Synthesis, spectroscopy, crystal structure, electrochemistry, and quantum chemical and molecular dynamics calculations of a 3-anilino difluoroboron dipyrromethene dye
Qin, Wenwu,Leen, Volker,Rohand, Taoufik,Dehaen, Wim,Dedecker, Peter,Van Der Auweraer, Mark,Robeyns, Koen,Van Meervelt, Luc,Beljonne, David,Van Averbeke, Bernard,Clifford, John N.,Driesen, Kris,Binnemans, Koen,Boens, Noel
, p. 439 - 447 (2009)
An asymmetrically substituted fluorescent difluoroboron dipyrromethene (BODIPY) dye, with a phenylamino group at the 3-position of the BODIPY chromophore, has been synthesized by nucleophilic substitution of 3,5-dichloro-8-(4-tolyl)-4,4-difluoro-4-bora-3a
BODIPY-based ratiometric fluorescent sensor for highly selective detection of glutathione over cysteine and homocysteine
Niu, Li-Ya,Guan, Ying-Shi,Chen, Yu-Zhe,Wu, Li-Zhu,Tung, Chen-Ho,Yang, Qing-Zheng
supporting information, p. 18928 - 18931 (2013/01/15)
We report a ratiometric fluorescent sensor based on monochlorinated BODIPY for highly selective detection of glutathione (GSH) over cysteine (Cys)/homocysteine (Hcy). The chlorine of the monochlorinated BODIPY can be rapidly replaced by thiolates of bioth
Functionalisation of fluorescent BODIPY dyes by nucleophilic substitution
Rohand, Taoufik,Baruah, Mukulesh,Qin, Wenwu,Boens, Noel,Dehaen, Wim
, p. 266 - 268 (2008/02/08)
The BODIPY chromophore can be easily modified by nucleophilic mono- or disubstitution of 3,5-dichloroBODIPY with O-, N-, S- and C-nucleophiles. Absorption and fluorescence spectral data of the new BODIPY derivatives are also reported. The Royal Society of
