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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:10.1016/j.ica.2025.122948</dc:identifier><dc:language>eng</dc:language><dc:creator>Kordestani, Nazanin</dc:creator><dc:creator>Martinez-Aguilera, Alvaro</dc:creator><dc:creator>Abas, Elisa</dc:creator><dc:creator>Grasa, Laura</dc:creator><dc:creator>Scalambra, Franco</dc:creator><dc:creator>Romerosa, Antonio</dc:creator><dc:title>Synthesis, characterizacion and study of novel heterobimetallic RAPTA-type Ru(II) complexes</dc:title><dc:identifier>ART-2025-145790</dc:identifier><dc:description>The new monometallic RAPTA complex [RuCl2(η6-p-cym)(dmPTA-κP)](CF3SO3)2 (1) and novel heterobimetallic complexes [RuCl2(η6-p-cym)-μ-(dmoPTA)-(1κP:2κ2N,N′-M(L)Cl2)] (M = Cu (3); M = Cu, L = DMF (3·3DMF); M = Pd (4)) have been synthesized and characterized (dmPTA = N,N′-dimethyl-1,3,5-triaza-7-phosphaadamantane; dmoPTA = 3,7-dimethyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane). The synthesized complexes have been fully characterized by elemental analysis and spectroscopic techniques. The crystal structure of the complexes 2, 3·3DMF and 4 were determined by single-crystal X-ray diffraction. The stability of complexes was studied in water and DMSO at room temperature and 37 °C. The anticancer activity against intestinal Caco-2/TC7 cells was studied.</dc:description><dc:date>2025</dc:date><dc:source>http://zaguan.unizar.es/record/163729</dc:source><dc:doi>10.1016/j.ica.2025.122948</dc:doi><dc:identifier>http://zaguan.unizar.es/record/163729</dc:identifier><dc:identifier>oai:zaguan.unizar.es:163729</dc:identifier><dc:identifier.citation>INORGANICA CHIMICA ACTA 589 (2025), 122948 [9 pp.]</dc:identifier.citation><dc:rights>by-nc</dc:rights><dc:rights>https://creativecommons.org/licenses/by-nc/4.0/deed.es</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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