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Probing the use of long lived intra-ligand π-π * excited states for photocatalytic systems: a study of the photophysics and photochemistry of [ReCl(CO)3(dppz-(CH3)2)]

Summers, Peter A.; Calladine, James A.; Ibrahim, Nasiru; Kusumo, Kennedy P.; Clark, Charlotte A.; Sun, Xue-Z.; Hamilton, Michelle L.; Towrie, Michael; McMaster, Jonathan; Schr�der, Martin; George, Michael W.

Probing the use of long lived intra-ligand π-π * excited states for photocatalytic systems: a study of the photophysics and photochemistry of [ReCl(CO)3(dppz-(CH3)2)] Thumbnail


Authors

Peter A. Summers

James A. Calladine

Nasiru Ibrahim

Kennedy P. Kusumo

Michelle L. Hamilton

Michael Towrie

Martin Schr�der



Abstract

We report the excited state photophysics and photochemistry of [ReCl(CO)3(dppz-(CH3)2)] (dppz-(CH3)2 = 11,12-dimethyl-dipyrido[3,2-a:2’,3’-c]phenazine) in CH3CN using timeresolved infrared (TRIR) and Fourier transform infrared (FTIR) spectroscopy. Excitation of the 1MLCT (metal-to-ligand charge transfer) band of [ReCl(CO)3(dppz-(CH3)2)] populates a 3MLCT excited state which rapidly interconverts on a timescale < 1 ns to a long lived IL (intra-ligand) π-π* excited state with a lifetime of 190 (± 5) ns. In the presence of an electron donor (NEt3), the IL excited state of [ReCl(CO)3(dppz-(CH3)2)] can be reductively quenched to [ReCl(CO)3(dppz-(CH3)2)]− with the radical in the latter localised on the distal phenazine (phz) portion of the dppz ligand. The phz based electron in [ReCl(CO)3(dppz-(CH3)2)]− has minimal interaction with the rhenium metal centre which increases the stability of the photosensitiser in its reduced form. In non-dried, non-degassed CH3CN (1 M NEt3), [ReCl(CO)3(dppz-(CH3)2)]− shows no significant change in the carbonyl region of the IR spectrum for at least 2 hours during continuous photolysis. In addition, we investigate the use of [ReCl(CO)3(dppz-(CH3)2)]− to reduce the previously studied catalyst [NiFe2], with facile electron transfer from [ReCl(CO)3(dppz-(CH3)2)]− to form [NiFe2]–.

Citation

Summers, P. A., Calladine, J. A., Ibrahim, N., Kusumo, K. P., Clark, C. A., Sun, X., …George, M. W. (2017). Probing the use of long lived intra-ligand π-π * excited states for photocatalytic systems: a study of the photophysics and photochemistry of [ReCl(CO)3(dppz-(CH3)2)]. Polyhedron, 123, 259-264. https://doi.org/10.1016/j.poly.2016.11.005

Journal Article Type Article
Acceptance Date Aug 15, 2016
Online Publication Date Nov 12, 2016
Publication Date Feb 17, 2017
Deposit Date Sep 13, 2017
Publicly Available Date Sep 13, 2017
Journal Polyhedron
Print ISSN 0277-5387
Electronic ISSN 0277-5387
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 123
Pages 259-264
DOI https://doi.org/10.1016/j.poly.2016.11.005
Keywords Rhenium ; Time-resolved IR ; Photophysics ; Intra-ligand excited state ; Reductive quenching
Public URL https://nottingham-repository.worktribe.com/output/845392
Publisher URL http://www.sciencedirect.com/science/article/pii/S0277538716305836?via%3Dihub
Additional Information This article is maintained by: Elsevier; Article Title: Probing the use of long lived intra-ligand π–π* excited states for photocatalytic systems: A study of the photophysics and photochemistry of [ReCl(CO)3(dppz-(CH3)2)]; Journal Title: Polyhedron; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.poly.2016.11.005; Content Type: article; Copyright: © 2016 Published by Elsevier Ltd.

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