Photoinduced electron transfer in ruthenium(II) trisbipyridine complexes connected to a naphthalenebisimide via an oligo(phenyleneethynylene) spacer

Frédérique Chaignon, Fabien Buchet, Errol Blart, Magnus Falkenström, Leif Hammarström, Fabrice Odobel

Research output: Contribution to journalArticle

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Abstract

The preparation and the characterization of three new dyads composed of a ruthenium trisbipyridine complex linked to a naphthalene bisimide electron acceptor via a phenyleneethynylene spacer of different length (one or two units) are reported. The dyads also differ by the anchoring position of the spacer on the bipyridine, which is appended either at the 4-position or the 5-position. Cyclic voltammetry and the UV-Vis absorption spectroscopy suggested that the spacer linked at the 5-position ensures a longer π-conjugation length but the electron transfer rates indicate a lower electronic coupling, than in 4-position. Photoinduced emission yields indicate a significant quenching of the MLCT excited-state of the ruthenium complex in these dyads. Except for the dyad linked in 5 position with one phenyleneethynylene unit, the transient absorption spectroscopy of all the other dyads evidences that the MLCT excited-state decays almost exclusively by electron transfer to form the charge-separated state RuIII-NBI-. This state could not be observed, presumably because the subsequent recombination to the ground state was much faster than its formation. In the dyad linked in 5 position with only one phenyleneethynylene unit, at room temperature, the 3MLCT* state is in equilibrium with the 3NBI* state, and it also decays via electron transfer. The notable feature of these dyads is first the occurrence of a relatively long-range electron transfer reaction via a bis(phenylethynylene) linking unit anchored at the 5 position. Secondly, we show within these series of compounds that subtle variations in the structure of the dyads (length of the spacer and anchoring position on bipy) have a strong impact on the rates and in the mechanism of decay of the 3MLCT* state. The photophysical properties of the dyads can be explained in terms of energy proximity of different excited states and magnitude of the electronic coupling according to the anchoring position.

Original languageEnglish
Pages (from-to)408-416
Number of pages9
JournalNew Journal of Chemistry
Volume33
Issue number2
DOIs
Publication statusPublished - 2009

Fingerprint

Ruthenium
Excited states
Electrons
Absorption spectroscopy
Naphthalene
Ultraviolet spectroscopy
Ground state
Cyclic voltammetry
Quenching
phenyleneethynylene
Temperature

ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Materials Chemistry

Cite this

Photoinduced electron transfer in ruthenium(II) trisbipyridine complexes connected to a naphthalenebisimide via an oligo(phenyleneethynylene) spacer. / Chaignon, Frédérique; Buchet, Fabien; Blart, Errol; Falkenström, Magnus; Hammarström, Leif; Odobel, Fabrice.

In: New Journal of Chemistry, Vol. 33, No. 2, 2009, p. 408-416.

Research output: Contribution to journalArticle

Chaignon, Frédérique ; Buchet, Fabien ; Blart, Errol ; Falkenström, Magnus ; Hammarström, Leif ; Odobel, Fabrice. / Photoinduced electron transfer in ruthenium(II) trisbipyridine complexes connected to a naphthalenebisimide via an oligo(phenyleneethynylene) spacer. In: New Journal of Chemistry. 2009 ; Vol. 33, No. 2. pp. 408-416.
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