Transient Intermediates from Mn(salen) with Sterically Hindered Mesityl Groups: Interconversion between MnIV-Phenolate and MnIII-Phenoxyl Radicals as an Origin for Unique Reactivity-Reference-Cited by-同舟云学术

Transient Intermediates from Mn(salen) with Sterically Hindered Mesityl Groups: Interconversion between MnIV-Phenolate and MnIII-Phenoxyl Radicals as an Origin for Unique Reactivity

Published:2008-02-01 Issue:5 Volume:47 Page:1674-1686
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Kurahashi Takuya¹,Kikuchi Akihiro¹,Tosha Takehiko¹,Shiro Yoshitsugu¹,Kitagawa Teizo¹,Fujii Hiroshi¹

Affiliation:

1. Institute for Molecular Science & Okazaki Institute for Integrative Bioscience, National Institutes of Natural Sciences, Myodaiji, Okazaki, Aichi 444-8787, Japan, and RIKEN SPring-8 Center, Harima Institute, 1-1-1, Kouto, Sayo, Hyogo 679-5148, Japan

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic702061y

Reference89 articles.

1. Metalloporphyrins as versatile catalysts for oxidation reactions and oxidative DNA cleavage

2. Epoxidation of olefins with cationic (salen)manganese(III) complexes. The modulation of catalytic activity by substituents

3. Enantioselective epoxidation of unfunctionalized olefins catalyzed by salen manganese complexes

4. Enantioselective epoxidation of unfunctionalized olefins using chiral (salen)manganese(III) complexes

5. Chromium− and Manganese−salen Promoted Epoxidation of Alkenes

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