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A general synthetic route to [Cu(X)(NHC)] (NHC = N-heterocyclic carbene, X = Cl, Br, I) complexes
Item metadata
| dc.contributor.author | Santoro, Orlando | |
| dc.contributor.author | Collado-Martinez, Alba | |
| dc.contributor.author | Slawin, Alexandra Martha Zoya | |
| dc.contributor.author | Nolan, Steven Patrick | |
| dc.contributor.author | Cazin, Catherine S.J. | |
| dc.date.accessioned | 2014-09-04T12:31:01Z | |
| dc.date.available | 2014-09-04T12:31:01Z | |
| dc.date.issued | 2013 | |
| dc.identifier.citation | Santoro , O , Collado-Martinez , A , Slawin , A M Z , Nolan , S P & Cazin , C S J 2013 , ' A general synthetic route to [Cu(X)(NHC)] (NHC = N-heterocyclic carbene, X = Cl, Br, I) complexes ' , Chemical Communications , vol. 49 , pp. 10483-10485 . https://doi.org/10.1039/c3cc45488f | en |
| dc.identifier.issn | 1359-7345 | |
| dc.identifier.other | PURE: 76967148 | |
| dc.identifier.other | PURE UUID: 56e48e07-dde5-40e9-92e9-2cf42186164a | |
| dc.identifier.other | Scopus: 84885642865 | |
| dc.identifier.other | ORCID: /0000-0002-9527-6418/work/56862107 | |
| dc.identifier.uri | http://hdl.handle.net/10023/5345 | |
| dc.description.abstract | A one-pot procedure for the synthesis of [Cu(X)(NHC)] (X = Cl, Br, I) is reported. The reaction is applicable to a wide range of saturated and unsaturated NHC ligands, is scalable and proceeds under mild conditions using technical grade solvents in air. | |
| dc.format.extent | 3 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Chemical Communications | en |
| dc.rights | © 2012. The Royal Society of Chemistry. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. | en |
| dc.subject | QD Chemistry | en |
| dc.subject.lcc | QD | en |
| dc.title | A general synthetic route to [Cu(X)(NHC)] (NHC = N-heterocyclic carbene, X = Cl, Br, I) complexes | en |
| dc.type | Journal article | en |
| dc.description.version | Publisher PDF | en |
| dc.contributor.institution | University of St Andrews. School of Chemistry | en |
| dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
| dc.identifier.doi | https://doi.org/10.1039/c3cc45488f | |
| dc.description.status | Peer reviewed | en |
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