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[Fe IV=O(TBC)(CH 3CN)] 2+: Comparative reactivity of iron(IV)-oxo species with constrained equatorial cyclam ligation

Title
[Fe IV=O(TBC)(CH 3CN)] 2+: Comparative reactivity of iron(IV)-oxo species with constrained equatorial cyclam ligation
Authors
Wilson S.A.Chen J.Hong S.Lee Y.-M.Clemancey M.Garcia-Serres R.Nomura T.Ogura T.Latour J.-M.Hedman B.Hodgson K.O.Nam W.Solomon E.I.
Ewha Authors
남원우이용민
SCOPUS Author ID
남원우scopus; 이용민scopusscopus
Issue Date
2012
Journal Title
Journal of the American Chemical Society
ISSN
0002-7863JCR Link
Citation
vol. 134, no. 28, pp. 11791 - 11806
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
[Fe IV=O(TBC)(CH 3CN)] 2+ (TBC = 1,4,8,11-tetrabenzyl-1,4,8,11-tetraazacyclotetradecane) is characterized, and its reactivity differences relative to [Fe IV=O(TMC)(CH 3CN)] 2+ (TMC = 1,4,8,11-tetramethyl-1,4,8,11- tetraazacyclotetradecane) are evaluated in hydrogen atom (H-atom) abstraction and oxo-transfer reactions. Structural differences are defined using X-ray absorption spectroscopy and correlated to reactivities using density functional theory. The S = 1 ground states are highly similar and result in large activation barriers (∼25 kcal/mol) due to steric interactions between the cyclam chelate and the substrate (e.g., ethylbenzene) associated with the equatorial π-attack required by this spin state. Conversely, H-atom abstraction reactivity on an S = 2 surface allows for a σ-attack with an axial substrate approach. This results in decreased steric interactions with the cyclam and a lower barrier (∼9 kcal/mol). For [Fe IV=O(TBC) (CH 3CN)] 2+, the S = 2 excited state in the reactant is lower in energy and therefore more accessible at the transition state due to a weaker ligand field associated with the steric interactions of the benzyl substituents with the trans-axial ligand. This study is further extended to the oxo-transfer reaction, which is a two-electron process requiring both σ- and π-electron transfer and thus a nonlinear transition state. In oxo-transfer, the S = 2 has a lower barrier due to sequential vs concerted (S = 1) two electron transfer which gives a high-spin ferric intermediate at the transition state. The [Fe IV=O(TBC)(CH 3CN)] 2+ complex is more distorted at the transition state, with the iron farther out of the equatorial plane due to the steric interaction of the benzyl groups with the trans-axial ligand. This allows for better orbital overlap with the substrate, a lower barrier, and an increased rate of oxo-transfer. © 2012 American Chemical Society.
DOI
10.1021/ja3046298
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자연과학대학 > 화학·나노과학전공 > Journal papers
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