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dc.contributor.authorKapturkiewicz, Aen_US
dc.contributor.authorChen, TMen_US
dc.contributor.authorLaskar, IRen_US
dc.contributor.authorNowacki, Jen_US
dc.date.accessioned2014-12-08T15:38:44Z-
dc.date.available2014-12-08T15:38:44Z-
dc.date.issued2004-08-01en_US
dc.identifier.issn1388-2481en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.elecom.2004.06.006en_US
dc.identifier.urihttp://hdl.handle.net/11536/26500-
dc.description.abstractElectrogenerated chemiluminescence (ECL) studies have been performed for the iridium(III) cyclometalated L2Ir(acac) complexes with substituted 2-phenylbenzothiazole ligand L. Electron transfer (ET) generation of the excited (3)*L2Ir(acac) has been studied using a triple-potential-step technique in acetonitrile-dioxane (1:1) solutions containing 0.1 M (n-C4H9)(4)NPF6 as the supporting electrolyte. ET reactions between electrochemically generated L2Ir(acac)(+) and A(-) (radical anions of aromatic nitriles) species lead to very efficient generation of ECL emission. Extremely high ECL efficiencies (up to 0.40) close to the excited (3)*L2Ir(acac) luminescence yields have been found. (C) 2004 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectelectrogenerated chemiluminescenceen_US
dc.subjectiridium complexesen_US
dc.subjectMLCT excited stateen_US
dc.titleElectrochemiluminescence studies of the cyclometalated iridium(III) complexes with substituted 2-phenylbenzothiazole ligandsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.elecom.2004.06.006en_US
dc.identifier.journalELECTROCHEMISTRY COMMUNICATIONSen_US
dc.citation.volume6en_US
dc.citation.issue8en_US
dc.citation.spage827en_US
dc.citation.epage831en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000222894600017-
dc.citation.woscount38-
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