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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1039/c8dt00298c</dc:identifier><dc:language>eng</dc:language><dc:creator>Fernández-Moreira, V.</dc:creator><dc:creator>Val-Campillo, C.</dc:creator><dc:creator>Ospino, I.</dc:creator><dc:creator>Herrera, R.P.</dc:creator><dc:creator>Marzo, I.</dc:creator><dc:creator>Laguna, A.</dc:creator><dc:creator>Gimeno, M.C.</dc:creator><dc:title>Bioactive and luminescent indole and isatin based gold(i) derivatives</dc:title><dc:identifier>ART-2019-111275</dc:identifier><dc:description>A series of luminescent monometallic [AuL(PPh 3 )] (1-3) and bimetallic [Au 2 (µ-dppe)L 2 ] (4, 6, 8) and [Au 2 (µ-dppp)L 2 ] (5, 7, 9) complexes, where L is either 4-cyano-indole, isatin, or 5, 7-dimethyl-isatin, and dppe and dppp are 1, 2-bis(diphenylphosphino)ethane and 1, 3-bis(diphenylphosphino)propane, respectively, have been synthesised. X-ray diffraction confirmed the tendency to establish aurophillic interations for those complexes containing dppe. Luminescence studies and theoretical calculations revealed a different origin for both families, i.e. indole and isatin species. Thus, indole derivatives presented a ligand-to-ligand-charge-transfer transition (LLCT) from the indole to the PPh 3 fragment, whereas for the isatin derivatives an intraligand-charge-transfer transition (ILCT) within the isatin fragment is proposed. In both cases, the gold centre was slightly implicated as a ligand-to-metal-charge transfer transition (LMCT) (from the indole/isatin to Au(i)). Cell antiproliferative assays in lung cancer cells (A549), leukemia Jurkat-pLVTHM and Jurkat-shBak cells (cisplatin sensitive and resistant, respectively) showed excellent cytotoxic values (10.11-0.28 µM), showing the leukemia cells to be the most sensitive and the bimetallic species to be the most active agents. Preliminary studies associated the cytotoxicity with a combination of different factors, the metallic fragment being mainly responsible. Remarkably, these complexes are able to inhibit the cellular growth of cisplatin resistant Jurkat-shBak cells highlighting their promising future as an alternative anticancer agent.</dc:description><dc:date>2019</dc:date><dc:source>http://zaguan.unizar.es/record/87700</dc:source><dc:doi>10.1039/c8dt00298c</dc:doi><dc:identifier>http://zaguan.unizar.es/record/87700</dc:identifier><dc:identifier>oai:zaguan.unizar.es:87700</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA-FSE/E07-17R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO-FEDER/CTQ2016-75816-C2-1-P</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO-FEDER/CTQ2017-88091-P</dc:relation><dc:identifier.citation>Dalton Transactions 48, 9 (2019), 3098-3108</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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