Controlling the energy and electron transfer in a novel ruthenium bipyridyl complex: An ESR study

Eylon Yavin, Lev Weiner, Rina Arad-Yellin, Abraham Shanzer*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

A novel ruthenium complex has been synthesized. It is composed of three bipyridyl ligands, one of which is modified and has two hydroxamate groups. Photoexcitation of the complex with blue light (λmax = 477 nm) leads to the formation of a long-lived nitroxyl radical on hydroxamate as was detected and characterized by ESR. In anaerobic conditions, the radical was not formed, suggesting that a reactive oxygen species is required for generating the nitroxyl radical. The quenching of the excited state of ruthenium bipyridyl complexes by molecular oxygen can generate either singlet oxygen via energy transfer or superoxide radical via electron transfer. In this latter case the superoxide radical is confined in a cage complex (vide infra). Singlet oxygen, generated via energy transfer from Ru(II) in its excited state, is the reactive species that is responsible for the oxidation of the hydroxamate group to its corresponding nitroxyl radical. This was confirmed by using a specific quencher (sodium azide) and by following the kinetics of the nitroxyl radical formation in deuterated solvents. Moreover, we can turn on the electron-transfer pathway by liberating superoxide radicals and producing a strong oxidant, Ru(III), from the collision "cage" complex proposed earlier (Zhang, X.; Rodgers, M.A.J. J. Phys. Chem. 1995, 99, 12797-12803.) This was achieved using compounds with either chemical (spin traps) or enzymatic (superoxide dismutase) affinity to superoxide radicals. Thus, the rate and yield of the nitroxyl radical formation in the novel ruthenium complex can be increased by almost thirty times.

Original languageAmerican English
Pages (from-to)8018-8024
Number of pages7
JournalJournal of Physical Chemistry A
Volume105
Issue number34
DOIs
StatePublished - 30 Aug 2001
Externally publishedYes

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