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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Bibliographic Details
Published inJournal of organometallic chemistry Vol. 957; p. 122155
Main Authors Dindar, Sara, Nemati Kharat, Ali, Abbasi, Alireza
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.01.2022
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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. [Display omitted]
ISSN:0022-328X
1872-8561
DOI:10.1016/j.jorganchem.2021.122155