Electrochromic and electrofluorochromic properties of a new boron dipyrromethene–ferrocene conjugate


Autoria(s): Galangau, O.; Fabre-Francke, I.; Munteanu, S.; Dumas-Verdes, C.; Clavier, G.; Méallet-Renault, R.; Pansu, R.B.; Hartl, Frantisek; Miomandre, F.
Data(s)

01/01/2013

Resumo

A new boron dipyrromethene–ferrocene (BODIPY–Fc) conjugate with pentafluorophenyl as the meso substituent and two Fc termini was synthesized and its spectroscopic and electrochemical features were analyzed. An intramolecular charge transfer from the donor Fc to the acceptor BODIPY has been predicted by theory and confirmed experimentally, leading to efficient fluorescence quenching when the dyad is in the neutral state. Fluorescence can be triggered by oxidizing both ferrocenyl units either chemically or electrochemically. Eventually, a fully reversible fluorescence switch is evidenced by coupling TIRF microscopy with electrolysis in an electrochemical cell.

Formato

text

Identificador

http://centaur.reading.ac.uk/30231/1/PK12-106R1-4%20-FH.pdf

Galangau, O., Fabre-Francke, I., Munteanu, S., Dumas-Verdes, C., Clavier, G., Méallet-Renault, R., Pansu, R.B., Hartl, F. <http://centaur.reading.ac.uk/view/creators/90000964.html> and Miomandre, F. (2013) Electrochromic and electrofluorochromic properties of a new boron dipyrromethene–ferrocene conjugate. Electrochimica Acta, 87. pp. 809-815. ISSN 0013-4686 doi: 10.1016/j.electacta.2012.09.048 <http://dx.doi.org/10.1016/j.electacta.2012.09.048>

Idioma(s)

en

Publicador

Elsevier

Relação

http://centaur.reading.ac.uk/30231/

creatorInternal Hartl, Frantisek

10.1016/j.electacta.2012.09.048

Tipo

Article

PeerReviewed