Experiment and theory reveal the fundamental difference between two-state and single-state reactivity patterns in nonheme FeIV=O versus Ru IV=O oxidants
Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review
Author(s)
Detail(s)
Original language | English |
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Pages (from-to) | 3356-3359 |
Journal / Publication | Angewandte Chemie - International Edition |
Volume | 47 |
Issue number | 18 |
Publication status | Published - 21 Apr 2008 |
Externally published | Yes |
Link(s)
Abstract
(Chemical Equation Presented) Two-state reactivity involving close triplet ground and quintet excited states is responsible for the opposite reactivity trends of FeIV oxo complexes in O-transfer and H-abstraction reactions in dependence on the electron richness of the axial ligand X (see picture), as shown by comparison with RuIV analogues, in which both reactivities are solely governed by the electrophilicity of the complex because the quintet state is inaccessible. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.
Research Area(s)
- Bioinorganic chemistry, Iron, Oxo ligands, Reaction mechanisms, Ruthenium
Citation Format(s)
Experiment and theory reveal the fundamental difference between two-state and single-state reactivity patterns in nonheme FeIV=O versus Ru IV=O oxidants. / Dhuri, Sunder N.; Mi, Sook Seo; Lee, Yong-Min et al.
In: Angewandte Chemie - International Edition, Vol. 47, No. 18, 21.04.2008, p. 3356-3359.Research output: Journal Publications and Reviews (RGC: 21, 22, 62) › 21_Publication in refereed journal › peer-review