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            <subfield code="a">Fernández-Moreira, V.</subfield>
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            <subfield code="a">Bioactive and luminescent indole and isatin based gold(i) derivatives</subfield>
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            <subfield code="c">2019</subfield>
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            <subfield code="a">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.</subfield>
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            <subfield code="a">Inorganic Chemistry</subfield>
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            <subfield code="a">Val-Campillo, C.</subfield>
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            <subfield code="a">Herrera, R.P.</subfield>
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            <subfield code="a">Marzo, I.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="1">1002</subfield>
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            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Bioq.Biolog.Mol. Celular</subfield>
            <subfield code="c">Área Biología Celular</subfield>
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            <subfield code="g">48, 9 (2019), 3098-3108</subfield>
            <subfield code="p">Dalton Trans.</subfield>
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