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Accueil > Recherche > Publications / brevets > Publications équipe ENSEMBLE > Publications Moléc nanomat fluo > Publications BODIPY

Rational design of visible and NIR distyryl-BODIPY dyes from a novel fluorinated platform.

Olivier Galangau, Cécile Dumas-Verdes, Rachel Méallet-Renault, Gilles Clavier; Org. Biomol. Chem., 8 (2010), 4546-4553.

Références :

Org. Biomol. Chem., 8 (2010), 4546-4553.

Auteur(s) : 

Olivier Galangau, Cécile Dumas-Verdes, Rachel Méallet-Renault, Gilles Clavier

A new series of distyryl-BODIPY has been rationally designed and synthesised from a novel fluorinated platform, 8-pentafluorophenylBODIPY, which has enhanced reactivity in the presence of both electron rich, and for the first time, electron deficient aldehydes. The pentafluorobenzene leads to larger red shifts of absorption and emission compared to previously reported analogues. The reactivity and spectroscopic results have been rationalised with quantum mechanics calculation. The fluorescence sensitivity of one derivative to acidity is also presented.

résumé graphique

résumé graphique


Type :
Publication
Dates :
Paru le 21 octobre 2010
Informations complémentaires :

DOI: 10.1039/c004812g


 

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