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Article: Trans [OR=eV-OH] core stabilised by chelating N-heterocyclic dicarbene ligands

TitleTrans [OR=eV-OH] core stabilised by chelating N-heterocyclic dicarbene ligands
Authors
Issue Date2013
Citation
Dalton Transactions, 2013, v. 42, n. 4, p. 871-873 How to Cite?
AbstractThree Re(v) N-heterocyclic carbene complexes [ReO(OH)(LMe) 2][PF6]1.4[ReO4]0.6, [ReO(OH)(LiPr)2][PF6]1.4[ReO 4]0.6 and [ReO(OH)(LBn)2][PF 6]1.3[ReO4]0.7 (LMe = 1,1′-methylene-bis(3-methylimidazole-2-ylidene); LiPr = 1,1′-methylene-bis(3-isopropylimidazole-2-ylidene) and LBn = 1,1′-methylene-bis(3-benzylimidazole-2-ylidene)) with trans oxo and hydroxo at axial positions have been synthesized. © The Royal Society of Chemistry 2013.
Persistent Identifierhttp://hdl.handle.net/10722/219684
ISSN
2021 Impact Factor: 4.569
2020 SCImago Journal Rankings: 0.980
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLum, Regina-
dc.contributor.authorZhang, Hu-
dc.contributor.authorZhang, Wenhua-
dc.contributor.authorBai, Shi Qiang-
dc.contributor.authorZhao, Jin-
dc.contributor.authorHor, T. S Andy-
dc.date.accessioned2015-09-23T02:57:43Z-
dc.date.available2015-09-23T02:57:43Z-
dc.date.issued2013-
dc.identifier.citationDalton Transactions, 2013, v. 42, n. 4, p. 871-873-
dc.identifier.issn1477-9226-
dc.identifier.urihttp://hdl.handle.net/10722/219684-
dc.description.abstractThree Re(v) N-heterocyclic carbene complexes [ReO(OH)(LMe) 2][PF6]1.4[ReO4]0.6, [ReO(OH)(LiPr)2][PF6]1.4[ReO 4]0.6 and [ReO(OH)(LBn)2][PF 6]1.3[ReO4]0.7 (LMe = 1,1′-methylene-bis(3-methylimidazole-2-ylidene); LiPr = 1,1′-methylene-bis(3-isopropylimidazole-2-ylidene) and LBn = 1,1′-methylene-bis(3-benzylimidazole-2-ylidene)) with trans oxo and hydroxo at axial positions have been synthesized. © The Royal Society of Chemistry 2013.-
dc.languageeng-
dc.relation.ispartofDalton Transactions-
dc.titleTrans [OR=eV-OH] core stabilised by chelating N-heterocyclic dicarbene ligands-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/c2dt31681a-
dc.identifier.pmid23172573-
dc.identifier.scopuseid_2-s2.0-84871940002-
dc.identifier.volume42-
dc.identifier.issue4-
dc.identifier.spage871-
dc.identifier.epage873-
dc.identifier.eissn1477-9234-
dc.identifier.isiWOS:000312659200005-
dc.identifier.issnl1477-9226-

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