Photoinduced electron transfer in platinum(II) terpyridinyl acetylide complexes connected to a porphyrin unit

Cyrille Monnereau, Julio Gomez, Errol Blart, Fabrice Odobel, Staffan Wallin, Anna Fallberg, Leif Hammarström

Research output: Contribution to journalArticle

52 Citations (Scopus)

Abstract

A series of six new dyads consisting of a zinc or magnesium porphyrin appended to a platinum terpyridine acetylide complex via a para-phenylene bisacetylene spacer are described. Different substituents on the 4′ position of the terpyridinyl ligand were explored (OC7H15, PO3Et2, and H). The ground-state electronic properties of the dyads are studied by electronic absorption spectroscopy and electrochemistry, and they indicate some electronic interactions between the porphyrin subunit and the platinum complex. The photophysical properties of these dyads were investigated by steady-state, time-resolved, and femtosecond transient absorption spectroscopy in N,N-dimethylformamide solution. Excitation of the porphyrin unit leads to a very rapid electron transfer (2-20 ps) to the nearby platinum complex followed by an ultrafast charge recombination, thus preventing any observation of the charge separated state. The variation in the rate of the photoinduced electron transfer in the series of dyads is consistent with Marcus theory. The results underscore the potential of the para-phenylene bisacetylene bridge to mediate a rapid electron transfer over a long donor-acceptor distance.

Original languageEnglish
Pages (from-to)4806-4817
Number of pages12
JournalInorganic Chemistry
Volume44
Issue number13
DOIs
Publication statusPublished - Jun 27 2005

    Fingerprint

ASJC Scopus subject areas

  • Inorganic Chemistry

Cite this