CO Oxidation by N2O Homogeneously Catalyzed by Ruthenium Hydride Pincer Complexes Indicating a New Mechanism
Author(s) -
Rong Zeng,
Moran Feller,
Yael DiskinPosner,
Linda J. W. Shimon,
Yehoshoa BenDavid,
David Milstein
Publication year - 2018
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.8b03927
Subject(s) - chemistry , catalysis , pincer movement , intramolecular force , ruthenium , hydride , ligand (biochemistry) , pincer ligand , photochemistry , medicinal chemistry , combinatorial chemistry , stereochemistry , organic chemistry , metal , receptor , biochemistry
Both CO and N 2 O are important, environmentally harmful industrial gases. The reaction of CO and N 2 O to produce CO 2 and N 2 has stimulated much research interest aimed at degradation of these two gases in a single step. Herein, we report an efficient CO oxidation by N 2 O catalyzed by a (PNN)Ru-H pincer complex under mild conditions, even with no added base. The reaction is proposed to proceed through a sequence of O-atom transfer (OAT) from N 2 O to the Ru-H bond to form a Ru-OH intermediate, followed by intramolecular OH attack on an adjacent CO ligand, forming CO 2 and N 2 . Thus, the Ru-H bond of the catalyst plays a central role in facilitating the OAT from N 2 O to CO, providing an efficient and novel protocol for CO oxidation.
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