Please use this identifier to cite or link to this item: https://doi.org/10.1021/om800410m
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dc.titleSwitching on the phosphorescence of pyrene by cycloplatination
dc.contributor.authorHu, J.
dc.contributor.authorYip, J.H.K.
dc.contributor.authorMa, D.-L.
dc.contributor.authorWong, K.-Y.
dc.contributor.authorChung, W.-H.
dc.date.accessioned2014-10-16T08:42:37Z
dc.date.available2014-10-16T08:42:37Z
dc.date.issued2009-01-12
dc.identifier.citationHu, J., Yip, J.H.K., Ma, D.-L., Wong, K.-Y., Chung, W.-H. (2009-01-12). Switching on the phosphorescence of pyrene by cycloplatination. Organometallics 28 (1) : 51-59. ScholarBank@NUS Repository. https://doi.org/10.1021/om800410m
dc.identifier.issn02767333
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94996
dc.description.abstract1-Diphenylphosphinopyrene (1-PyP) and 1,6-bis(diphenylphosphino)pyrene (1,6-PyP) can be metalated at C5 and C10 to give cyclometalated complexes [M(L)(1-PyP-H)]+ and [M2(L)2(1,6-PyP)] 2+ (M = Pd or Pt, L = diphosphines). The π-π* transitions of the pyrenyl ring are strongly perturbed by the PPh2 groups at C1/6, while the perturbation of the metal ions at C5/10 is weak. The phosphorescence of the pyrenyl ring is strongly enhanced by the heavy atom effect of the Pt ion up to a quantum yield of 1.5 × 10-2. Direct coordination of the Pt ion to the pyrenyl ring is needed for enhancement of the phosphorescence. © 2009 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/om800410m
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/om800410m
dc.description.sourcetitleOrganometallics
dc.description.volume28
dc.description.issue1
dc.description.page51-59
dc.description.codenORGND
dc.identifier.isiut000262177200008
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