Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2768
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dc.contributor.authorKaur, Gurpreet-
dc.contributor.authorChoudhury, A.R.-
dc.date.accessioned2020-12-07T10:35:43Z-
dc.date.available2020-12-07T10:35:43Z-
dc.date.issued2014-
dc.identifier.citationDalton Transactions, 43(43), pp.16431-16440.en_US
dc.identifier.otherhttps://doi.org/10.1039/C4DT02266A-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2014/dt/c4dt02266a#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/123456789/2768-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractDesign and syntheses of 'aggregation induced emission (AIE)' active blue-emitting bis-cyclometalated iridium(iii) complexes with appended diphosphine ligands [Ir(F2ppy)2(L1/L2)2(Cl)] (F2ppy = 2-(2′,4′-difluoro) phenylpyridine; L1 = 1,2-bis(diphenylphosphino)ethane; L2 = bis(diphenylphosphino)propane) have been realized on a suitable route. The free phosphorous donor atom present on the appended diphosphine is shown to provide selective binding to the mercuric ion (Hg2+). The selective binding ability of the probe molecule towards mercuric ions results in a detectable signal due to complete quenching of their AIE properties. The quenching effect of the probe molecule has been explored and found to be the result of the degradation of the probe iridium(iii) complex triggered by the presence of mercuric ions due to an interplay of a soft-soft interaction between the free phosphorous atom of the probe molecule and mercuric ions. These complexes were modelled to obtain deeper understanding of excited state properties and the results were tentatively correlated with the experimental data.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectPhosphorescent Sensorsen_US
dc.subjectCyclometalateden_US
dc.subjectIridiumen_US
dc.titleNew ‘aggregation induced emission (AIE)’ active cyclometalated iridium(iii) based phosphorescent sensors: high sensitivity for mercury(ii) ionsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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