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Issue 12, 2017
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Photoisomerization of ruthenium(II) aquo complexes: mechanistic insights and application development

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Abstract

Ruthenium(II) complexes with polypyridyl ligands have been extensively studied as promising functional molecules due to their unique photochemical and photophysical properties as well as redox properties. In this context, we report the photoisomerization of distal-[Ru(tpy)(pynp)OH2]2+ (d-1) (tpy = 2,2′;6′,2′′-terpyridine, pynp = 2-(2-pyridyl)-1,8-naphthyridine) to proximal-[Ru(tpy)(pynp)OH2]2+ (p-1), which has not been previously characterized for polypyridyl ruthenium(II) aquo complexes. Herein, we review recent progress made by our group on the mechanistic insights and application developments related to the photoisomerization of polypyridyl ruthenium(II) aquo complexes. We report a new strategic synthesis of dinuclear ruthenium(II) complexes that can act as an active water oxidation catalyst, as well as the development of unique visible-light-responsive giant vesicles, both of which were achieved based on photoisomerization.

Graphical abstract: Photoisomerization of ruthenium(ii) aquo complexes: mechanistic insights and application development

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Publication details

The article was received on 10 Jan 2017, accepted on 14 Feb 2017 and first published on 15 Feb 2017


Article type: Perspective
DOI: 10.1039/C7DT00079K
Citation: Dalton Trans., 2017,46, 3787-3799
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    Photoisomerization of ruthenium(II) aquo complexes: mechanistic insights and application development

    M. Hirahara and M. Yagi, Dalton Trans., 2017, 46, 3787
    DOI: 10.1039/C7DT00079K

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