Please use this identifier to cite or link to this item:
https://doi.org/10.1039/c1dt10789e
DC Field | Value | |
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dc.title | Syntheses and characterizations of thiolato-functionalized N-heterocyclic carbene Pd(ii) complexes with normal and mesoionic binding modes | |
dc.contributor.author | Yuan, D. | |
dc.contributor.author | Huynh, H.V. | |
dc.date.accessioned | 2014-10-16T08:42:44Z | |
dc.date.available | 2014-10-16T08:42:44Z | |
dc.date.issued | 2011-11-28 | |
dc.identifier.citation | Yuan, 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.issn | 14779226 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/95007 | |
dc.description.abstract | The 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.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c1dt10789e | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1039/c1dt10789e | |
dc.description.sourcetitle | Dalton Transactions | |
dc.description.volume | 40 | |
dc.description.issue | 44 | |
dc.description.page | 11698-11703 | |
dc.identifier.isiut | 000296776200007 | |
Appears in Collections: | Staff Publications |
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