<?xml version="1.0" encoding="UTF-8"?>
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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.dyepig.2025.112641</dc:identifier><dc:language>eng</dc:language><dc:creator>Melendo, Irene</dc:creator><dc:creator>Camacho-Aguayo, Javier</dc:creator><dc:creator>Fuertes, Sara</dc:creator><dc:creator>Martín, Antonio</dc:creator><dc:creator>Marcos, Susana de</dc:creator><dc:creator>Galbán, Javier</dc:creator><dc:creator>Sicilia, Violeta</dc:creator><dc:title>Sizing-up the aromatic system of a Cyclometalated n-Heterocyclic Carbene in a luminescent platinum-based sensor to xanthine</dc:title><dc:identifier>ART-2025-141562</dc:identifier><dc:description>A cyclometalated N-heterocyclic carbene platinum(II) complex comprising a phenanthrenyl moiety has been prepared and used to synthesize neutral and cationic luminescent complexes containing different ancillary ligands: [Pt(PhenˆC*)(acac)] (5), [Pt(PhenˆC*)(CNXyl)2]PF6 (6) and [Pt(PhenˆC*)(PˆP)]PF6 (PˆP: 1,1-bis(diphenylphosphino)methane, dppm 7; 1,2-bis(diphenylphosphino)ethane, dppe, 8, 1,2-bis(diphenylphosphino)benzene, dppbz, 9). Structural characterization by NMR and single-crystal X-ray studies endorsed the proposed molecular structure for these complexes with the formation of a six-membered platinacycle. Photophysical and computational studies for 5-9 disclosed the ligand-centered nature of the triplet state, mainly governed by the extended aromatic system of the PhenˆC* ligand. Immobilized in ethyl cellulose (EC) films, compound 5 shows elevated quantum yield and long decay times in argon atmosphere and high sensitivity to molecular oxygen. Blends of 5 and EC (C5) were tested as a luminescent oxygen probe for the determination of xanthine (Xn), showing good photo stability and reversibility. The RSD is 0.9% (n=3) for 3·10-4 M and the detection limit achieves values of ∼ 2·10-5 M. This platinum-based sensor delivers better results than the ones obtained with [Ru(bpy)3]Cl2·6 H2O, a typical luminophore used in commercial oxygen sensors. To improve the feasibility of the Xn determination, the sensor was implemented in a smartphone adapted device to be used as a in-situ Xn control.</dc:description><dc:date>2025</dc:date><dc:source>http://zaguan.unizar.es/record/148121</dc:source><dc:doi>10.1016/j.dyepig.2025.112641</dc:doi><dc:identifier>http://zaguan.unizar.es/record/148121</dc:identifier><dc:identifier>oai:zaguan.unizar.es:148121</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E17-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/DGA/E25-23R</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2021-122869NB-I00</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MICINN/PID2022-139235OB-I00</dc:relation><dc:identifier.citation>Dyes and Pigments 235 (2025), 112641 [36 pp.]</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/embargoedAccess</dc:rights></dc:dc>

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