Convenient and Reusable Manganese‐Based Nanocatalyst for Amination of Alcohols
The development of new sustainable nanocatalytic systems for green chemical synthesis is a growing area in chemical science. Herein, a reusable heterogeneous N‐doped graphene‐based manganese nanocatalyst (Mn@NrGO) for selective N‐alkylation of amines with alcohols is described. Mechanistic studies i...
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creator | Subaramanian, Murugan Ramar, Palmurukan M. Sivakumar, Ganesan Kadam, Ravishankar G. Petr, Martin Zboril, Radek Gawande, Manoj B. Balaraman, Ekambaram |
description | The development of new sustainable nanocatalytic systems for green chemical synthesis is a growing area in chemical science. Herein, a reusable heterogeneous N‐doped graphene‐based manganese nanocatalyst (Mn@NrGO) for selective N‐alkylation of amines with alcohols is described. Mechanistic studies illustrate that the catalytic reaction follows a domino dehydrogenation‐condensation‐hydrogenation sequence of alcohols and amines with the formation of water as the sole by‐product. The scope of the reaction is extended to the synthesis of pharmaceutically important N‐alkylated amine intermediates. The heterogeneous nature of the catalyst made it easy to separate for long‐term performance, and the recycling study revealed that the catalyst was robust and retained its activity after several recycling experiments.
Nanocatalytic Amination: Herein, a reusable heterogeneous N‐doped graphene‐based manganese nanocatalyst (Mn@NrGO) for selective N‐alkylation of amines with alcohols is described. The heterogeneous nature of the catalyst made it easy to separate for long‐term performance, and the recycling study revealed that the catalyst was robust and retained its activity after several recycling experiments. |
doi_str_mv | 10.1002/cctc.202100635 |
format | Article |
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Nanocatalytic Amination: Herein, a reusable heterogeneous N‐doped graphene‐based manganese nanocatalyst (Mn@NrGO) for selective N‐alkylation of amines with alcohols is described. The heterogeneous nature of the catalyst made it easy to separate for long‐term performance, and the recycling study revealed that the catalyst was robust and retained its activity after several recycling experiments.</description><identifier>ISSN: 1867-3880</identifier><identifier>EISSN: 1867-3899</identifier><identifier>DOI: 10.1002/cctc.202100635</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Alcohol ; Alcohols ; Alkylation ; Amination ; Amines ; Catalysts ; Chemical synthesis ; Condensates ; Dehydrogenation ; Graphene ; Heterogeneous catalysis ; Hydrogen ; Manganese ; Manganese catalyst ; Recycling ; Sustainable development</subject><ispartof>ChemCatChem, 2021-10, Vol.13 (20), p.4334-4341</ispartof><rights>2021 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3835-7ae25ef6121888ac737399bf9b9b0ecabeb34060cf3f47f5de122e553738e54a3</citedby><cites>FETCH-LOGICAL-c3835-7ae25ef6121888ac737399bf9b9b0ecabeb34060cf3f47f5de122e553738e54a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcctc.202100635$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcctc.202100635$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids></links><search><creatorcontrib>Subaramanian, Murugan</creatorcontrib><creatorcontrib>Ramar, Palmurukan M.</creatorcontrib><creatorcontrib>Sivakumar, Ganesan</creatorcontrib><creatorcontrib>Kadam, Ravishankar G.</creatorcontrib><creatorcontrib>Petr, Martin</creatorcontrib><creatorcontrib>Zboril, Radek</creatorcontrib><creatorcontrib>Gawande, Manoj B.</creatorcontrib><creatorcontrib>Balaraman, Ekambaram</creatorcontrib><title>Convenient and Reusable Manganese‐Based Nanocatalyst for Amination of Alcohols</title><title>ChemCatChem</title><description>The development of new sustainable nanocatalytic systems for green chemical synthesis is a growing area in chemical science. Herein, a reusable heterogeneous N‐doped graphene‐based manganese nanocatalyst (Mn@NrGO) for selective N‐alkylation of amines with alcohols is described. Mechanistic studies illustrate that the catalytic reaction follows a domino dehydrogenation‐condensation‐hydrogenation sequence of alcohols and amines with the formation of water as the sole by‐product. The scope of the reaction is extended to the synthesis of pharmaceutically important N‐alkylated amine intermediates. The heterogeneous nature of the catalyst made it easy to separate for long‐term performance, and the recycling study revealed that the catalyst was robust and retained its activity after several recycling experiments.
Nanocatalytic Amination: Herein, a reusable heterogeneous N‐doped graphene‐based manganese nanocatalyst (Mn@NrGO) for selective N‐alkylation of amines with alcohols is described. The heterogeneous nature of the catalyst made it easy to separate for long‐term performance, and the recycling study revealed that the catalyst was robust and retained its activity after several recycling experiments.</description><subject>Alcohol</subject><subject>Alcohols</subject><subject>Alkylation</subject><subject>Amination</subject><subject>Amines</subject><subject>Catalysts</subject><subject>Chemical synthesis</subject><subject>Condensates</subject><subject>Dehydrogenation</subject><subject>Graphene</subject><subject>Heterogeneous catalysis</subject><subject>Hydrogen</subject><subject>Manganese</subject><subject>Manganese catalyst</subject><subject>Recycling</subject><subject>Sustainable development</subject><issn>1867-3880</issn><issn>1867-3899</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkMtOwzAQRS0EEqWwZW2JdYpjx4m9LBEvqTyEytqauGNIldolTkHd8Ql8I19CqqKyZDV3pHNnpEPIacpGKWP83NrOjjjj_ZILuUcGqcqLRCit93dZsUNyFOO8R7Qo5IA8lsG_o6_RdxT8jD7hKkLVIL0D_wIeI35_fl1AxBm9Bx8sdNCsY0ddaOl4UXvo6uBpcHTc2PAamnhMDhw0EU9-55A8X11Oy5tk8nB9W44niRVKyKQA5BJdnvJUKQW2EIXQunK60hVDCxVWImM5s064rHByhinnKGWPKZQZiCE5295dtuFthbEz87Bqff_ScKlEryDjRU-NtpRtQ4wtOrNs6wW0a5Mys7FmNtbMzlpf0NvCR93g-h_alOW0_Ov-ALMLceM</recordid><startdate>20211019</startdate><enddate>20211019</enddate><creator>Subaramanian, Murugan</creator><creator>Ramar, Palmurukan M.</creator><creator>Sivakumar, Ganesan</creator><creator>Kadam, Ravishankar G.</creator><creator>Petr, Martin</creator><creator>Zboril, Radek</creator><creator>Gawande, Manoj B.</creator><creator>Balaraman, Ekambaram</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20211019</creationdate><title>Convenient and Reusable Manganese‐Based Nanocatalyst for Amination of Alcohols</title><author>Subaramanian, Murugan ; Ramar, Palmurukan M. ; Sivakumar, Ganesan ; Kadam, Ravishankar G. ; Petr, Martin ; Zboril, Radek ; Gawande, Manoj B. ; Balaraman, Ekambaram</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3835-7ae25ef6121888ac737399bf9b9b0ecabeb34060cf3f47f5de122e553738e54a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alcohol</topic><topic>Alcohols</topic><topic>Alkylation</topic><topic>Amination</topic><topic>Amines</topic><topic>Catalysts</topic><topic>Chemical synthesis</topic><topic>Condensates</topic><topic>Dehydrogenation</topic><topic>Graphene</topic><topic>Heterogeneous catalysis</topic><topic>Hydrogen</topic><topic>Manganese</topic><topic>Manganese catalyst</topic><topic>Recycling</topic><topic>Sustainable development</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Subaramanian, Murugan</creatorcontrib><creatorcontrib>Ramar, Palmurukan M.</creatorcontrib><creatorcontrib>Sivakumar, Ganesan</creatorcontrib><creatorcontrib>Kadam, Ravishankar G.</creatorcontrib><creatorcontrib>Petr, Martin</creatorcontrib><creatorcontrib>Zboril, Radek</creatorcontrib><creatorcontrib>Gawande, Manoj B.</creatorcontrib><creatorcontrib>Balaraman, Ekambaram</creatorcontrib><collection>CrossRef</collection><jtitle>ChemCatChem</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Subaramanian, Murugan</au><au>Ramar, Palmurukan M.</au><au>Sivakumar, Ganesan</au><au>Kadam, Ravishankar G.</au><au>Petr, Martin</au><au>Zboril, Radek</au><au>Gawande, Manoj B.</au><au>Balaraman, Ekambaram</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Convenient and Reusable Manganese‐Based Nanocatalyst for Amination of Alcohols</atitle><jtitle>ChemCatChem</jtitle><date>2021-10-19</date><risdate>2021</risdate><volume>13</volume><issue>20</issue><spage>4334</spage><epage>4341</epage><pages>4334-4341</pages><issn>1867-3880</issn><eissn>1867-3899</eissn><abstract>The development of new sustainable nanocatalytic systems for green chemical synthesis is a growing area in chemical science. Herein, a reusable heterogeneous N‐doped graphene‐based manganese nanocatalyst (Mn@NrGO) for selective N‐alkylation of amines with alcohols is described. Mechanistic studies illustrate that the catalytic reaction follows a domino dehydrogenation‐condensation‐hydrogenation sequence of alcohols and amines with the formation of water as the sole by‐product. The scope of the reaction is extended to the synthesis of pharmaceutically important N‐alkylated amine intermediates. The heterogeneous nature of the catalyst made it easy to separate for long‐term performance, and the recycling study revealed that the catalyst was robust and retained its activity after several recycling experiments.
Nanocatalytic Amination: Herein, a reusable heterogeneous N‐doped graphene‐based manganese nanocatalyst (Mn@NrGO) for selective N‐alkylation of amines with alcohols is described. The heterogeneous nature of the catalyst made it easy to separate for long‐term performance, and the recycling study revealed that the catalyst was robust and retained its activity after several recycling experiments.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/cctc.202100635</doi><tpages>8</tpages></addata></record> |
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subjects | Alcohol Alcohols Alkylation Amination Amines Catalysts Chemical synthesis Condensates Dehydrogenation Graphene Heterogeneous catalysis Hydrogen Manganese Manganese catalyst Recycling Sustainable development |
title | Convenient and Reusable Manganese‐Based Nanocatalyst for Amination of Alcohols |
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