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2016 Fiscal Year Final Research Report

Control of oxidation reactivity of (peroxo)diiron complexes

Research Project

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Project/Area Number 26410067
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Inorganic chemistry
Research InstitutionKanazawa University

Principal Investigator

Furutachi Hideki  金沢大学, 物質化学系, 准教授 (40332663)

Project Period (FY) 2014-04-01 – 2017-03-31
Keywords二核鉄ペルオキソ錯体 / 酸素分子活性化 / アレーン水酸化 / 機能モデル / 反応中間体 / 酸化反応 / X線結晶構造解析 / 高原子価鉄オキソ種
Outline of Final Research Achievements

The Fe2/O2-mediated oxidation reactions such as arene hydroxylation and C-H bond oxidation of alkanes are of current interest for understanding the reaction mechanism of dioxygen activating non-heme diiron enzymes such as soluble methane monooxygenase (sMMO) and toluene monooxygenase (TMO) and utilizing metal complexes as oxidation catalysis. Various synthetic (peroxo)diiron(III) model complexes have been developed, however, there are few functional models that exhibit oxidation reactivity and O-O bond cleavage similar to those of (peroxo)diiron(III) species in non-heme diiron enzymes. In this study, (peroxo)diiron(III) complexes having a bridging ligand (oxo or carboxylate) were prepared and their oxidation reacvtivities towards external substrates were studied. We found a mechanistic evidence that a diiron(IV)-oxo species derived from the O-O bond cleavage of (peroxo)diiron(III) species is involved in the oxidation reaction as an active oxidant.

Free Research Field

生物無機化学

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Published: 2018-03-22  

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