Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/40146
Title: Efficient acceptorless dehydrogenation of secondary alcohols to ketones mediated by a PNN-Ru(II) catalyst
Authors: Wang, Zheng
Pan, Bing
Liu, Qingbin
Yue, Erlin
Solan, Gregory A.
Ma, Yanping
Sun, Wen-Hua
First Published: 31-Mar-2017
Publisher: Royal Society of Chemistry
Citation: Catalysis Science and Technology, 2017, 7, 1654-1661
Abstract: Four types of ruthenium(II) complexes, [fac-PNN]RuH(PPh3)(CO) (A), [fac-PNHN]RuH(η1-BH4)(CO) (B), [fac-PNHN]RuCl2(PPh3) (C) and [fac-PNHN]RuH(η1-BH4)(PPh3) (D) (where PNHN and PNN are N-(2-(diphenylphosphino)ethyl)-5,6,7,8-tetrahydroquinoline-8-amine and its deprotonated derivative), have been synthesized and assessed as catalysts for the acceptorless dehydrogenation of secondary alcohols to afford ketones. It was found that C, in combination with t-BuOK, proved the most effective and versatile catalyst allowing aromatic-, aliphatic- and cycloalkyl-containing alcohols to be efficiently converted to their corresponding ketones with particularly high values of TON achievable. Furthermore, the mechanism for this PNN-Ru mediated process been proposed on the basis of a number of intermediates that have been characterized by EI-MS and NMR spectroscopy. These catalysts show great potential for applications in atom-economic synthesis as well as in the development of organic hydride-based hydrogen storage systems.
DOI Link: 10.1039/c7cy00342k
ISSN: 2044-4753
eISSN: 2044-4761
Links: http://pubs.rsc.org/en/Content/ArticleLanding/2017/CY/C7CY00342K#!divAbstract
http://hdl.handle.net/2381/40146
Embargo on file until: 31-Mar-2018
Version: Post-print
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © 2017, Royal Society of Chemistry. Deposited with reference to the publisher’s open access archiving policy.
Description: The file associated with this record is under embargo until 12 months after publication, in accordance with the publisher's self-archiving policy. The full text may be available through the publisher links provided above.
Appears in Collections:Published Articles, Dept. of Chemistry

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