Abstract
A mononuclear nonheme manganese(III)-acylperoxo complex bearing a simple picolylamine-based linear ligand was synthesized and characterized by various spectroscopic methods along with theoretical calculations. The reactivity of the manganese(III)-acylperoxo complex was investigated in the oxygen atom transfer, C-H and O-H bond activation reactions. The oxidations of organic substrates followed first-order kinetics with respect to substrates and featured nonradical-type, suggesting that the manganese(III)-acylperoxo complex was the reactive oxidant. The C-H bond activation of hydrocarbon and the O-H bond activation of alcohol proceeded via a rate-limiting H-atom abstraction reaction in a concerted manner.
Original language | English |
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Pages (from-to) | 1513-1518 |
Number of pages | 6 |
Journal | Bulletin of the Korean Chemical Society |
Volume | 42 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2021 |
Bibliographical note
Funding Information:National Research Foundation of Korea Funding information
Publisher Copyright:
© 2021 Korean Chemical Society, Seoul & Wiley-VCH GmbH
Keywords
- acylperoxo
- C-H bond activation
- concerted mechanism
- phenol oxidation
- reactive intermediate