z-logo
Premium
An Iron(III)–Monoamidate Complex Catalyst for Selective Hydroxylation of Alkane CH Bonds with Hydrogen Peroxide
Author(s) -
Hitomi Yutaka,
Arakawa Kengo,
Funabiki Takuzo,
Kodera Masahito
Publication year - 2012
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201108933
Subject(s) - heterolysis , hydroxylation , hydrogen peroxide , chemistry , catalysis , radical , moiety , ligand (biochemistry) , combinatorial chemistry , alkane , peroxide , medicinal chemistry , photochemistry , organic chemistry , stereochemistry , biochemistry , receptor , enzyme
Selective oxidation : The success of the title reaction (see scheme) is caused by the strong electron donation from the amidate moiety of the dpaq ligand to the iron center (dpaq=2‐[bis(pyridin‐2‐ylmethyl)]amino‐ N ‐quinolin‐8‐yl‐acetamidate). This process facilitates the OO bond heterolysis of the intermediate Fe III OOH species to generate a selective oxidant without forming highly reactive hydroxyl radicals.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom