4.6 Review

Emission Spectroscopy as a Probe into Photoinduced Intramolecular Electron Transfer in Polyazine Bridged Ru(II),Rh(III) Supramolecular Complexes

Journal

MATERIALS
Volume 3, Issue 8, Pages 4328-4354

Publisher

MDPI AG
DOI: 10.3390/ma3084328

Keywords

emission spectroscopy; MLCT light absorbers; polyazine bridging ligands; supramolecular; intramolecular electron transfer

Funding

  1. Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Sciences, U.S. Department of Energy

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Steady-state and time-resolved emission spectroscopy are valuable tools to probe photochemical processes of metal-ligand, coordination complexes. Ru(II) polyazine light absorbers are efficient light harvesters absorbing in the UV and visible with emissive (MLCT)-M-3 excited states known to undergo excited state energy and electron transfer. Changes in emission intensity, energy or band-shape, as well as excited state lifetime, provide insight into excited state dynamics. Photophysical processes such as intramolecular electron transfer between electron donor and electron acceptor sub-units may be investigated using these methods. This review investigates the use of steady-state and time-resolved emission spectroscopy to measure excited state intramolecular electron transfer in polyazine bridged Ru(II),Rh(III) supramolecular complexes. Intramolecular electron transfer in these systems provides for conversion of the emissive (MLCT)-M-3 (metal-to-ligand charge transfer) excited state to a non-emissive, but potentially photoreactive, (MMCT)-M-3 (metal-to-metal charge transfer) excited state. The details of the photophysics of Ru(II),Rh(III) and Ru(II),Rh(III),Ru(II) systems as probed by steady-state and time-resolved emission spectroscopy will be highlighted.

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