Femtosecond transient absorption anisotropy study on [Ru(bpy) 3]2+ and [Ru(bpy)(py)4]2+· ultrafast interligand randomization of the MLCT state

Staffan Wallin, Jan Davidsson, Judit Modin, Leif Hammarström

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125 Citations (Scopus)

Abstract

It is known that the relaxed excited state of [Ru(bpy)3] 2+ is best described as a metal to ligand charge transfer (MLCT) state having one formally reduced bipyridine and two neutral. Previous reports have suggested [Malone, R. et al. J. Chem. Phys. 1991, 95, 8970] that the electron "hops" from ligand to ligand in the MLCT state with a time constant of about 50 ps in acetonitrile. However, we have done transient absorption anisotropy measurements indicating that already after one picosecond the molecule has no memory of which bipyridine was initially photoselected, which suggests an ultrafast interligand randomization of the MLCT state.

Original languageEnglish
Pages (from-to)4697-4704
Number of pages8
JournalJournal of Physical Chemistry A
Volume109
Issue number21
DOIs
Publication statusPublished - Jun 2 2005

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Charge transfer
Anisotropy
Metals
charge transfer
Ligands
ligands
anisotropy
metals
Excited states
time constant
acetonitrile
tris(2,2'-bipyridine)ruthenium II
bis(bipyridyl)ruthenium(II)
Data storage equipment
Molecules
Electrons
excitation
molecules
electrons

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry

Cite this

Femtosecond transient absorption anisotropy study on [Ru(bpy) 3]2+ and [Ru(bpy)(py)4]2+· ultrafast interligand randomization of the MLCT state. / Wallin, Staffan; Davidsson, Jan; Modin, Judit; Hammarström, Leif.

In: Journal of Physical Chemistry A, Vol. 109, No. 21, 02.06.2005, p. 4697-4704.

Research output: Contribution to journalArticle

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