Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1dt10269a
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dc.titleCSC-pincer versus pseudo-pincer complexes of palladium(ii): A comparative study on complexation and catalytic activities of NHC complexes
dc.contributor.authorYuan, D.
dc.contributor.authorTang, H.
dc.contributor.authorXiao, L.
dc.contributor.authorHuynh, H.V.
dc.date.accessioned2014-06-23T05:35:21Z
dc.date.available2014-06-23T05:35:21Z
dc.date.issued2011-09-21
dc.identifier.citationYuan, D., Tang, H., Xiao, L., Huynh, H.V. (2011-09-21). CSC-pincer versus pseudo-pincer complexes of palladium(ii): A comparative study on complexation and catalytic activities of NHC complexes. Dalton Transactions 40 (35) : 8788-8795. ScholarBank@NUS Repository. https://doi.org/10.1039/c1dt10269a
dc.identifier.issn14779226
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75844
dc.description.abstractThree thioether bridged diimidazolium dibromides with different steric and electronic properties have been synthesized as precursors to carbene-based CSC pincer ligands. Palladation afforded CSC Pd(ii) pincer complexes for bulky and electron rich ligand systems, whereas the least donating ligand led to the formation of a pseudo-pincer complex. All complexes have been fully characterized by multinuclei NMR spectroscopies, ESI mass spectrometry and X-ray diffraction analysis. The catalytic activities of pincer versus pseudo-pincer complexes have been compared in the intermolecular hydroamination of alkynes with anilines as well. © The Royal Society of Chemistry 2011.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c1dt10269a
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c1dt10269a
dc.description.sourcetitleDalton Transactions
dc.description.volume40
dc.description.issue35
dc.description.page8788-8795
dc.identifier.isiut000294475500010
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