Loading…
Facile synthesis of NHC-stabilized Ni nanoparticles and their catalytic application in the Z-selective hydrogenation of alkynes
Well defined Ni nanoparticles (NiNPs) stabilized with N-heterocyclic carbenes (NHCs) have been synthesized through a new methodology involving the decarboxylation of a zwitterionic CO adduct. Their catalytic performance was tested in the partial hydrogenation of alkynes into (Z)-alkenes under very m...
Saved in:
Published in: | Chemical communications (Cambridge, England) England), 2017-07, Vol.53 (56), p.7894-7897 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c323t-1b4999cd9b234bf338fddcaf9a4ed66099566386ffd5d036aae5fcc1b26db57e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c323t-1b4999cd9b234bf338fddcaf9a4ed66099566386ffd5d036aae5fcc1b26db57e3 |
container_end_page | 7897 |
container_issue | 56 |
container_start_page | 7894 |
container_title | Chemical communications (Cambridge, England) |
container_volume | 53 |
creator | de Los Bernardos, Miriam Díaz Pérez-Rodríguez, Sara Gual, Aitor Claver, Carmen Godard, Cyril |
description | Well defined Ni nanoparticles (NiNPs) stabilized with N-heterocyclic carbenes (NHCs) have been synthesized through a new methodology involving the decarboxylation of a zwitterionic CO
adduct. Their catalytic performance was tested in the partial hydrogenation of alkynes into (Z)-alkenes under very mild reaction conditions (50 °C and 5 bar H
pressure), providing excellent activities and selectivities. |
doi_str_mv | 10.1039/c7cc01779k |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1896411765</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1896411765</sourcerecordid><originalsourceid>FETCH-LOGICAL-c323t-1b4999cd9b234bf338fddcaf9a4ed66099566386ffd5d036aae5fcc1b26db57e3</originalsourceid><addsrcrecordid>eNo9kE9LxDAQxYMouq5e_ACSowjVpGnS5ijFfyh6URAvJU0mbtxsWpuuUC9-dbvu6lxm3syPN_AQOqLkjBImz3WuNaF5LudbaEKZyBKeFS_bq5nLJGcZ30P7Mb6TsSgvdtFeWmQFkURM0PeV0s4DjkPoZxBdxI3FDzdlEntVO---wOAHh4MKTau63mkPEatg8Ei7DmvVKz-Ma6za1rtRuiZgF1Zn_JpE8KB79wl4NpiueYOwBsYfys-HAPEA7VjlIxxu-hQ9X10-lTfJ_eP1bXlxn2iWsj6hdSal1EbWKctqy1hhjdHKSpWBEYJIyYVghbDWcEOYUAq41ZrWqTA1z4FN0cnat-2ajyXEvlq4qMF7FaBZxooWUmSU5oKP6Oka1V0TYwe2aju3UN1QUVKtAq_KvCx_A78b4eON77JegPlH_xJmP_ddfok</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1896411765</pqid></control><display><type>article</type><title>Facile synthesis of NHC-stabilized Ni nanoparticles and their catalytic application in the Z-selective hydrogenation of alkynes</title><source>Royal Society of Chemistry Journals</source><creator>de Los Bernardos, Miriam Díaz ; Pérez-Rodríguez, Sara ; Gual, Aitor ; Claver, Carmen ; Godard, Cyril</creator><creatorcontrib>de Los Bernardos, Miriam Díaz ; Pérez-Rodríguez, Sara ; Gual, Aitor ; Claver, Carmen ; Godard, Cyril</creatorcontrib><description>Well defined Ni nanoparticles (NiNPs) stabilized with N-heterocyclic carbenes (NHCs) have been synthesized through a new methodology involving the decarboxylation of a zwitterionic CO
adduct. Their catalytic performance was tested in the partial hydrogenation of alkynes into (Z)-alkenes under very mild reaction conditions (50 °C and 5 bar H
pressure), providing excellent activities and selectivities.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/c7cc01779k</identifier><identifier>PMID: 28480906</identifier><language>eng</language><publisher>England</publisher><ispartof>Chemical communications (Cambridge, England), 2017-07, Vol.53 (56), p.7894-7897</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c323t-1b4999cd9b234bf338fddcaf9a4ed66099566386ffd5d036aae5fcc1b26db57e3</citedby><cites>FETCH-LOGICAL-c323t-1b4999cd9b234bf338fddcaf9a4ed66099566386ffd5d036aae5fcc1b26db57e3</cites><orcidid>0000-0002-2518-7401 ; 0000-0001-5762-4904</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28480906$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Los Bernardos, Miriam Díaz</creatorcontrib><creatorcontrib>Pérez-Rodríguez, Sara</creatorcontrib><creatorcontrib>Gual, Aitor</creatorcontrib><creatorcontrib>Claver, Carmen</creatorcontrib><creatorcontrib>Godard, Cyril</creatorcontrib><title>Facile synthesis of NHC-stabilized Ni nanoparticles and their catalytic application in the Z-selective hydrogenation of alkynes</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>Well defined Ni nanoparticles (NiNPs) stabilized with N-heterocyclic carbenes (NHCs) have been synthesized through a new methodology involving the decarboxylation of a zwitterionic CO
adduct. Their catalytic performance was tested in the partial hydrogenation of alkynes into (Z)-alkenes under very mild reaction conditions (50 °C and 5 bar H
pressure), providing excellent activities and selectivities.</description><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNo9kE9LxDAQxYMouq5e_ACSowjVpGnS5ijFfyh6URAvJU0mbtxsWpuuUC9-dbvu6lxm3syPN_AQOqLkjBImz3WuNaF5LudbaEKZyBKeFS_bq5nLJGcZ30P7Mb6TsSgvdtFeWmQFkURM0PeV0s4DjkPoZxBdxI3FDzdlEntVO---wOAHh4MKTau63mkPEatg8Ei7DmvVKz-Ma6za1rtRuiZgF1Zn_JpE8KB79wl4NpiueYOwBsYfys-HAPEA7VjlIxxu-hQ9X10-lTfJ_eP1bXlxn2iWsj6hdSal1EbWKctqy1hhjdHKSpWBEYJIyYVghbDWcEOYUAq41ZrWqTA1z4FN0cnat-2ajyXEvlq4qMF7FaBZxooWUmSU5oKP6Oka1V0TYwe2aju3UN1QUVKtAq_KvCx_A78b4eON77JegPlH_xJmP_ddfok</recordid><startdate>20170711</startdate><enddate>20170711</enddate><creator>de Los Bernardos, Miriam Díaz</creator><creator>Pérez-Rodríguez, Sara</creator><creator>Gual, Aitor</creator><creator>Claver, Carmen</creator><creator>Godard, Cyril</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2518-7401</orcidid><orcidid>https://orcid.org/0000-0001-5762-4904</orcidid></search><sort><creationdate>20170711</creationdate><title>Facile synthesis of NHC-stabilized Ni nanoparticles and their catalytic application in the Z-selective hydrogenation of alkynes</title><author>de Los Bernardos, Miriam Díaz ; Pérez-Rodríguez, Sara ; Gual, Aitor ; Claver, Carmen ; Godard, Cyril</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-1b4999cd9b234bf338fddcaf9a4ed66099566386ffd5d036aae5fcc1b26db57e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Los Bernardos, Miriam Díaz</creatorcontrib><creatorcontrib>Pérez-Rodríguez, Sara</creatorcontrib><creatorcontrib>Gual, Aitor</creatorcontrib><creatorcontrib>Claver, Carmen</creatorcontrib><creatorcontrib>Godard, Cyril</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Los Bernardos, Miriam Díaz</au><au>Pérez-Rodríguez, Sara</au><au>Gual, Aitor</au><au>Claver, Carmen</au><au>Godard, Cyril</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Facile synthesis of NHC-stabilized Ni nanoparticles and their catalytic application in the Z-selective hydrogenation of alkynes</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2017-07-11</date><risdate>2017</risdate><volume>53</volume><issue>56</issue><spage>7894</spage><epage>7897</epage><pages>7894-7897</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>Well defined Ni nanoparticles (NiNPs) stabilized with N-heterocyclic carbenes (NHCs) have been synthesized through a new methodology involving the decarboxylation of a zwitterionic CO
adduct. Their catalytic performance was tested in the partial hydrogenation of alkynes into (Z)-alkenes under very mild reaction conditions (50 °C and 5 bar H
pressure), providing excellent activities and selectivities.</abstract><cop>England</cop><pmid>28480906</pmid><doi>10.1039/c7cc01779k</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-2518-7401</orcidid><orcidid>https://orcid.org/0000-0001-5762-4904</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1359-7345 |
ispartof | Chemical communications (Cambridge, England), 2017-07, Vol.53 (56), p.7894-7897 |
issn | 1359-7345 1364-548X |
language | eng |
recordid | cdi_proquest_miscellaneous_1896411765 |
source | Royal Society of Chemistry Journals |
title | Facile synthesis of NHC-stabilized Ni nanoparticles and their catalytic application in the Z-selective hydrogenation of alkynes |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T18%3A39%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Facile%20synthesis%20of%20NHC-stabilized%20Ni%20nanoparticles%20and%20their%20catalytic%20application%20in%20the%20Z-selective%20hydrogenation%20of%20alkynes&rft.jtitle=Chemical%20communications%20(Cambridge,%20England)&rft.au=de%20Los%20Bernardos,%20Miriam%20D%C3%ADaz&rft.date=2017-07-11&rft.volume=53&rft.issue=56&rft.spage=7894&rft.epage=7897&rft.pages=7894-7897&rft.issn=1359-7345&rft.eissn=1364-548X&rft_id=info:doi/10.1039/c7cc01779k&rft_dat=%3Cproquest_cross%3E1896411765%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c323t-1b4999cd9b234bf338fddcaf9a4ed66099566386ffd5d036aae5fcc1b26db57e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1896411765&rft_id=info:pmid/28480906&rfr_iscdi=true |