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    <subfield code="a">10.1016/j.dyepig.2025.112641</subfield>
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    <subfield code="2">sideral</subfield>
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    <subfield code="a">eng</subfield>
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    <subfield code="a">Melendo, Irene</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Sizing-up the aromatic system of a Cyclometalated n-Heterocyclic Carbene in a luminescent platinum-based sensor to xanthine</subfield>
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    <subfield code="c">2025</subfield>
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    <subfield code="a">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.</subfield>
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    <subfield code="a">Camacho-Aguayo, Javier</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-1654-3803</subfield>
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    <subfield code="a">Fuertes, Sara</subfield>
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    <subfield code="a">Martín, Antonio</subfield>
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    <subfield code="a">Marcos, Susana de</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-7902-6005</subfield>
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    <subfield code="a">Galbán, Javier</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-8973-5104</subfield>
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    <subfield code="a">Sicilia, Violeta</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-0257-0483</subfield>
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    <subfield code="1">2010</subfield>
    <subfield code="2">760</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Inorgánica</subfield>
    <subfield code="c">Área Química Inorgánica</subfield>
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    <subfield code="1">2009</subfield>
    <subfield code="2">750</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Química Analítica</subfield>
    <subfield code="c">Área Química Analítica</subfield>
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    <subfield code="g">235 (2025), 112641 [36 pp.]</subfield>
    <subfield code="p">Dyes pigm.</subfield>
    <subfield code="t">Dyes and Pigments</subfield>
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