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- Publisher Website: 10.1021/acssuschemeng.0c05787
- Scopus: eid_2-s2.0-85096098764
- WOS: WOS:000588740300022
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Article: Hydrazine as facile nitrogen source for direct synthesis of amines over a supported Pt catalyst
Title | Hydrazine as facile nitrogen source for direct synthesis of amines over a supported Pt catalyst |
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Authors | |
Keywords | Heterogeneous catalysis Secondary amines Alcohols Hydrazine Supported Pt catalyst Aldehydes |
Issue Date | 2020 |
Citation | ACS Sustainable Chemistry and Engineering, 2020, v. 8, n. 43, p. 16283-16295 How to Cite? |
Abstract | Facile preparation of secondary amines from alcohols or aldehydes is achieved by using the hydrazine (N2H4) as an easy-to-handle nitrogen source. The anatase titania-supported Pt (Pt/TiO2-A) is discovered to be an efficient catalyst to enable the first alcohols/aldehydes to amines conversion with N2H4 as the only nitrogen and hydrogen source without any additional base or additives. Mechanistic studies suggest that this alcohol-to-amine transformation proceeds by the sequential alcohol dehydrogenation, aldehyde-N2H4 condensation, azine reduction, imine formation, and reduction processes in one pot. As N2H4 is a strong nucleophile that readily reacts with aldehyde, the unique catalytic property of Pt/TiO2-A ensures the high selectivity of amine products by providing multifunctional active sites for dehydrogenation and multiple reductions. This study highlights the considerable potential of hydrazine in direct synthesis of nitrogen-containing fine chemicals with a fine-tuned heterogeneous Pt catalyst, which is safe, green, and easy to handle. |
Persistent Identifier | http://hdl.handle.net/10722/299479 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Wang, Jing | - |
dc.contributor.author | Ye, Sen | - |
dc.contributor.author | Liu, Xiang | - |
dc.contributor.author | Loh, Teck Peng | - |
dc.date.accessioned | 2021-05-21T03:34:30Z | - |
dc.date.available | 2021-05-21T03:34:30Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | ACS Sustainable Chemistry and Engineering, 2020, v. 8, n. 43, p. 16283-16295 | - |
dc.identifier.uri | http://hdl.handle.net/10722/299479 | - |
dc.description.abstract | Facile preparation of secondary amines from alcohols or aldehydes is achieved by using the hydrazine (N2H4) as an easy-to-handle nitrogen source. The anatase titania-supported Pt (Pt/TiO2-A) is discovered to be an efficient catalyst to enable the first alcohols/aldehydes to amines conversion with N2H4 as the only nitrogen and hydrogen source without any additional base or additives. Mechanistic studies suggest that this alcohol-to-amine transformation proceeds by the sequential alcohol dehydrogenation, aldehyde-N2H4 condensation, azine reduction, imine formation, and reduction processes in one pot. As N2H4 is a strong nucleophile that readily reacts with aldehyde, the unique catalytic property of Pt/TiO2-A ensures the high selectivity of amine products by providing multifunctional active sites for dehydrogenation and multiple reductions. This study highlights the considerable potential of hydrazine in direct synthesis of nitrogen-containing fine chemicals with a fine-tuned heterogeneous Pt catalyst, which is safe, green, and easy to handle. | - |
dc.language | eng | - |
dc.relation.ispartof | ACS Sustainable Chemistry and Engineering | - |
dc.subject | Heterogeneous catalysis | - |
dc.subject | Secondary amines | - |
dc.subject | Alcohols | - |
dc.subject | Hydrazine | - |
dc.subject | Supported Pt catalyst | - |
dc.subject | Aldehydes | - |
dc.title | Hydrazine as facile nitrogen source for direct synthesis of amines over a supported Pt catalyst | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/acssuschemeng.0c05787 | - |
dc.identifier.scopus | eid_2-s2.0-85096098764 | - |
dc.identifier.hkuros | 327339 | - |
dc.identifier.volume | 8 | - |
dc.identifier.issue | 43 | - |
dc.identifier.spage | 16283 | - |
dc.identifier.epage | 16295 | - |
dc.identifier.eissn | 2168-0485 | - |
dc.identifier.isi | WOS:000588740300022 | - |