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Article: Additive-free N-methylation of amines with methanol over supported iridium catalyst

TitleAdditive-free N-methylation of amines with methanol over supported iridium catalyst
Authors
Issue Date2021
PublisherRoyal Society of Chemistry. The Journal's web site is located at http://pubs.rsc.org/en/Journals/JournalIssues/CY#!recentarticles&all
Citation
Catalysis Science & Technology, 2021, v. 11 n. 10, p. 3364-3375 How to Cite?
AbstractAn efficient and versatile zinc oxide-supported iridium (Ir/ZnO) catalyst was developed to catalyze the additive-free N-methylation of amines with methanol. Mechanistic studies suggested that the high catalytic reactivity is rooted in the small sizes (1.4 nm) of Ir nanoparticles and the high ratio (93%) of oxidized iridium species (IrOx, Ir3+ and Ir4+) on the catalyst. Moreover, the delicate cooperation between the IrOx and ZnO support also promoted its high reactivity. The selectivity of this catalytic N-methylation was controllable between dimethylation and monomethylation by carefully tuning the catalyst loading and reaction solvent. Specifically, neat methanol with high catalyst loading (2 mol% Ir) favored the formation of N,N-dimethylated amine, while the mesitylene/methanol mixture with low catalyst loading (0.5 mol% Ir) was prone to producing mono-N-methylated amines. An environmentally benign continuous flow system with a recycled mode was also developed for the efficient production of N-methylated amines. With optimal flow rates and amine concentrations, a variety of N-methylamines were produced with good to excellent yields in this Ir/ZnO-based flow system, providing a starting point for the clean and efficient production of N-methylamines with this cost-effective chemical process.
Persistent Identifierhttp://hdl.handle.net/10722/305279
ISSN
2021 Impact Factor: 6.177
2020 SCImago Journal Rankings: 1.635
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWang, J-
dc.contributor.authorQiang, W-
dc.contributor.authorYe, S-
dc.contributor.authorZhu, L-
dc.contributor.authorLiu, X-
dc.contributor.authorLoh, TP-
dc.date.accessioned2021-10-20T10:07:10Z-
dc.date.available2021-10-20T10:07:10Z-
dc.date.issued2021-
dc.identifier.citationCatalysis Science & Technology, 2021, v. 11 n. 10, p. 3364-3375-
dc.identifier.issn2044-4753-
dc.identifier.urihttp://hdl.handle.net/10722/305279-
dc.description.abstractAn efficient and versatile zinc oxide-supported iridium (Ir/ZnO) catalyst was developed to catalyze the additive-free N-methylation of amines with methanol. Mechanistic studies suggested that the high catalytic reactivity is rooted in the small sizes (1.4 nm) of Ir nanoparticles and the high ratio (93%) of oxidized iridium species (IrOx, Ir3+ and Ir4+) on the catalyst. Moreover, the delicate cooperation between the IrOx and ZnO support also promoted its high reactivity. The selectivity of this catalytic N-methylation was controllable between dimethylation and monomethylation by carefully tuning the catalyst loading and reaction solvent. Specifically, neat methanol with high catalyst loading (2 mol% Ir) favored the formation of N,N-dimethylated amine, while the mesitylene/methanol mixture with low catalyst loading (0.5 mol% Ir) was prone to producing mono-N-methylated amines. An environmentally benign continuous flow system with a recycled mode was also developed for the efficient production of N-methylated amines. With optimal flow rates and amine concentrations, a variety of N-methylamines were produced with good to excellent yields in this Ir/ZnO-based flow system, providing a starting point for the clean and efficient production of N-methylamines with this cost-effective chemical process.-
dc.languageeng-
dc.publisherRoyal Society of Chemistry. The Journal's web site is located at http://pubs.rsc.org/en/Journals/JournalIssues/CY#!recentarticles&all-
dc.relation.ispartofCatalysis Science & Technology-
dc.titleAdditive-free N-methylation of amines with methanol over supported iridium catalyst-
dc.typeArticle-
dc.identifier.emailYe, S: yesen@hku.hk-
dc.identifier.authorityYe, S=rp02805-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/D0CY02442B-
dc.identifier.scopuseid_2-s2.0-85107014999-
dc.identifier.hkuros327332-
dc.identifier.volume11-
dc.identifier.issue10-
dc.identifier.spage3364-
dc.identifier.epage3375-
dc.identifier.isiWOS:000634893700001-
dc.publisher.placeUnited Kingdom-

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