Reactivity of Compound II: Electronic Structure Analysis of Methane Hydroxylation by Oxoiron(IV) Porphyrin Complexes
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- 作者：Angela Rosa ; Giampaolo Ricciardi
- 刊名：Inorganic Chemistry
- 出版年：2012
- 出版时间：September 17, 2012
- 年：2012
- 卷：51
- 期：18
- 页码：9833-9845
- 全文大小：677K
- 年卷期：v.51,no.18(September 17, 2012)
- ISSN：1520-510X
文摘
The methane hydroxylation reaction by a Compound II (Cpd II) mimic PorFeIV=O and its hydrosulfide-ligated derivative [Por(SH)FeIV=O]鈭?/sup> is investigated by density functional theory (DFT) calculations on the ground triplet and excited quintet spin-state surfaces. On each spin surface both the 蟽- and 蟺-channels are explored. H-abstraction is invariably the rate-determining step. In the case of PorFeIV=O the H-abstraction reaction can proceed either through the classic 蟺-channel or through the nonclassical 蟽-channel on the triplet surface, but only through the classic 蟽-mechanism on the quintet surface. The barrier on the quintet 蟽-pathway is much lower than on the triplet channels so the quintet surface cuts through the triplet surfaces and a two state reactivity (TSR) mechanism with crossover from the triplet to the quintet surface becomes a plausible scenario for C鈥揌 bond activation by PorFeIV=O. In the case of the hydrosulfide-ligated complex the H-abstraction follows a 蟺-mechanism on the triplet surface: the 蟽* is too high in energy to make a 蟽-attack of the substrate favorable. The 蟽- and 蟺-channels are both feasible on the quintet surface. As the quintet surface lies above the triplet surface in the entrance channel of the oxidative process and is highly destabilized on both the 蟽- and 蟺-pathways, the reaction can only proceed on the triplet surface. Insights into the electron transfer process accompanying the H-abstraction reaction are achieved through a detailed electronic structure analysis of the transition state species and the reactant complexes en route to the transition state. It is found that the electron transfer from the substrate 蟽CH into the acceptor orbital of the catalyst, the Fe鈥揙 蟽* or 蟺*, occurs through a rather complex mechanism that is initiated by a two-orbital four-electron interaction between the 蟽CH and the low-lying, oxygen-rich Fe鈥揙 蟽-bonding and/or Fe鈥揙 蟺-bonding orbitals of the catalyst.