Green and chemo selective amine methylation using methanol by an organometallic ruthenium complex
•Synthesis and crystal structure of a novel ruthenium carbonyl complex, RuCl2(CO)(Xantphos) with a trident pincer mode for xanphos ligand.•Obtain a green and atom-efficient process for n-methylation amine with methanol under hydrogen autotransfer conditions.•High active and chemo-selective homougeno...
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Published in | Journal of organometallic chemistry Vol. 957; p. 122155 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.01.2022
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Subjects | |
Online Access | Get full text |
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Summary: | •Synthesis and crystal structure of a novel ruthenium carbonyl complex, RuCl2(CO)(Xantphos) with a trident pincer mode for xanphos ligand.•Obtain a green and atom-efficient process for n-methylation amine with methanol under hydrogen autotransfer conditions.•High active and chemo-selective homougenous catalytic system for N-methylation of aniline and hexylamine.
Herein a green and convenient catalytic N-methylation of aniline and n-hexylamine using methanol as a dual methylation agent and solvent has been investigated. A new ruthenium carbonyl complex was synthesized and applied as a homogeneous catalyst in methylation reaction. The solid-state structure of the complex was determined by X-ray crystallographic analysis which indicate xantphos ligand bonded to ruthenium (II) as a tridentate pincer ligand by two P donor and one O atom. The catalytic system showed excellent conversion and selectivity toward N-methylaniline, and N,N-hexyldimethylamine at 140°C.
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ISSN: | 0022-328X 1872-8561 |
DOI: | 10.1016/j.jorganchem.2021.122155 |