Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1dt10789e
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dc.titleSyntheses and characterizations of thiolato-functionalized N-heterocyclic carbene Pd(ii) complexes with normal and mesoionic binding modes
dc.contributor.authorYuan, D.
dc.contributor.authorHuynh, H.V.
dc.date.accessioned2014-10-16T08:42:44Z
dc.date.available2014-10-16T08:42:44Z
dc.date.issued2011-11-28
dc.identifier.citationYuan, D., Huynh, H.V. (2011-11-28). Syntheses and characterizations of thiolato-functionalized N-heterocyclic carbene Pd(ii) complexes with normal and mesoionic binding modes. Dalton Transactions 40 (44) : 11698-11703. ScholarBank@NUS Repository. https://doi.org/10.1039/c1dt10789e
dc.identifier.issn14779226
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95007
dc.description.abstractThe thiolato-bridged dimeric Pd(ii) NHC complex 1 has been synthesized from the reaction of thioester-functionalized imidazolium salt B and Pd(OAc) 2. The isolation of its interesting constitutional isomer 2 bearing both classical C(2)-bound and mesoionic C(4)-bound ligands coordinating to two different metal centers in the same complex allowed for a direct comparison of these isomeric carbenes. Reactivity studies of 1 with NaSCH(CH3) 2 and NaBF4 afforded the tetranuclear compound 3 with a [Pd4S4] macrocycle. All complexes have been fully characterized by multinuclei NMR spectroscopies, ESI mass spectrometry and X-ray diffraction analysis. This journal is © The Royal Society of Chemistry 2011.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c1dt10789e
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c1dt10789e
dc.description.sourcetitleDalton Transactions
dc.description.volume40
dc.description.issue44
dc.description.page11698-11703
dc.identifier.isiut000296776200007
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