Proton catalysis in the redox responsivity of a mini-sized photochromic diarylethene.
Chemistry
; 19(37): 12435-45, 2013 Sep 09.
Article
en En
| MEDLINE
| ID: mdl-23881753
ABSTRACT
A thermally irreversible dithienylethene (DTE) photochrom can be turned into a thermally reversible one in presence of Cu(II) triflate. A ring opening (DTEC closedâDTEO open) occurs through the formation of a copper-containing fast transient intermediate. Stopped-flow experiments monitored at 410 and 780â
nm have allowed to show that the stoichiometry of this intermediate is DTE/Cu=11. At longer monitoring times (i.e., several seconds after mixing), the intermediate undergoes a slow decay while the residual DTEC closed form opens. A joint detailed kinetic and electrochemical analysis has unveiled a proton catalysis scenario in which electron transfer between DTEC and Cu(II), ligand exchange, protonation-deprotonation equilibria of the cation radicals and ring opening are embedded into two main reaction cycles. At the beginning of the reaction, Cu(II) is reduced into Cu(I) and DTE is degraded without ring opening. Then, as the reaction progresses, the triflic acid released from the Cu(II) reduction switches-on a propagation cycle during which ring opens without any more Cu(II) consumption. Cyclic voltammetry, spectro-electrochemical measurements, delayed photocoloration experiments in presence of Cu(II) and acid-base additions have confirmed the main features of the proton catalysis.
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Colección:
01-internacional
Banco de datos:
MEDLINE
Idioma:
En
Revista:
Chemistry
Asunto de la revista:
QUIMICA
Año:
2013
Tipo del documento:
Article