Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0dt01380c
DC FieldValue
dc.titleN-heterocyclic carbene Pt(ii) complexes from caffeine: Synthesis, structures and photoluminescent properties
dc.contributor.authorHu, J.J.
dc.contributor.authorBai, S.-Q.
dc.contributor.authorYeh, H.H.
dc.contributor.authorYoung, D.J.
dc.contributor.authorChi, Y.
dc.contributor.authorHor, T.S.A.
dc.date.accessioned2014-10-16T08:35:07Z
dc.date.available2014-10-16T08:35:07Z
dc.date.issued2011-05-07
dc.identifier.citationHu, J.J., Bai, S.-Q., Yeh, H.H., Young, D.J., Chi, Y., Hor, T.S.A. (2011-05-07). N-heterocyclic carbene Pt(ii) complexes from caffeine: Synthesis, structures and photoluminescent properties. Dalton Transactions 40 (17) : 4402-4406. ScholarBank@NUS Repository. https://doi.org/10.1039/c0dt01380c
dc.identifier.issn14779226
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94362
dc.description.abstractThe caffeine-derived N-heterocyclic carbene (NHC) complex [Pt II(CN)(NHC)Cl] (CN = 2-phenylpyridine), 4 has the opposite stereochemistry and a shorter Pt-Ccarbene bond compared to that of an analogous benzimidazole-derived N,N-heterocyclic carbene (NNHC) Pt complex 2. These suggest a lower trans influence of pyridyl N compared to cyclometallated carbon and an increased Pt-NHC π-backbonding because of decreased π-donation resulting from conjugation to the electron deficient pyrimidine of caffeine. Complex 4 has a lower emission quantum yield (Φ) and is blue-shifted into the green region of the visible spectrum relative to non-carbene Pt(ii) cyclometalated complex 5. © 2011 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c0dt01380c
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c0dt01380c
dc.description.sourcetitleDalton Transactions
dc.description.volume40
dc.description.issue17
dc.description.page4402-4406
dc.identifier.isiut000289686600008
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