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               <dc:title>Binding Studies of a Luminescent Pt(II) Organometallic Calix[4]pyrrole with Halide Salts</dc:title>
               <dc:creator>Lázaro Palacios, Ariadna</dc:creator>
               <dc:creator>Valencia, Esteban</dc:creator>
               <dc:creator>Ballester, Pablo</dc:creator>
               <dc:creator>Rodríguez Raurell, Laura</dc:creator>
               <dc:subject>Compostos organometàl·lics</dc:subject>
               <dc:subject>Compostos d'halògens</dc:subject>
               <dc:subject>Química organometàl·lica</dc:subject>
               <dc:subject>Organometallic compounds</dc:subject>
               <dc:subject>Halogen compounds</dc:subject>
               <dc:subject>Organometallic chemistry</dc:subject>
               <dc:description>We report the synthesis of a luminescent Pt(II) complex, PtL2, based on a “two-wall” aryl-extended calix[4]pyrrole (C[4]P). We characterize its binding properties as a receptor of methyl trioctyl ammonium chloride (MTOA·Cl) in a dichloromethane solution. To this end, we performed 1H NMR and UV−vis spectroscopic titrations. The singular luminescent properties of PtL2 allowed the use of highly sensitive emission spectroscopy to&lt;/p>&lt;p>monitor the binding. The binding affinity of PtL2 for MTOA·Cl is 2-fold smaller than that of the C[4]P precursor. This difference is attributed to dissimilar anion−π interactions and binding geometries in the ion-paired complexes of the two receptors, (Cl⊂PtL2/C[4]P)@MTOA. Isothermal titration calorimetry (ITC) experiments revealed subtle differences in enthalpy and entropy. The entropic term, although negative, was very small, suggesting the relevance of the dissociation/association processes of the salt and the ion-paired complexes. We investigated the binding selectivity of PtL2 toward a series of halides in acetone solution favoring ion-pair dissociation. PtL2 binds chloride selectively and with a high affinity, producing mainly an anionic complex.</dc:description>
               <dc:date>2026-03-19T12:56:16Z</dc:date>
               <dc:date>2026-03-19T12:56:16Z</dc:date>
               <dc:date>2025-02-21</dc:date>
               <dc:date>2026-03-19T12:56:17Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
               <dc:relation>Reproducció del document publicat a: https://doi.org/10.1021/acsomega.4c11558</dc:relation>
               <dc:relation>ACS Omega, 2025, vol. 10, p. 8665-8674</dc:relation>
               <dc:relation>https://doi.org/10.1021/acsomega.4c11558</dc:relation>
               <dc:rights>cc-by-nc-nd (c) Lázaro, Adriana, et al., 2026</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>American Chemical Society</dc:publisher>
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