z-logo
open-access-imgOpen Access
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

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