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                  <mods:namePart>Bazaga-García, Montse</mods:namePart>
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                  <mods:namePart>Vílchez-Cózar, Álvaro</mods:namePart>
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                  <mods:namePart>Olivera-Pastor, Pascual</mods:namePart>
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                  <mods:namePart>Ilia, Gheorghe</mods:namePart>
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                  <mods:namePart>Cabeza-Díaz, Aurelio</mods:namePart>
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                  <mods:namePart>Visa, Aurelia</mods:namePart>
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                  <mods:namePart>Pérez-Colodrero, Rosario Mercedes</mods:namePart>
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               <mods:identifier type="citation">Dalton Trans., 2021, Accepted Manuscript; https://doi.org/10.1039/D1DT00104C</mods:identifier>
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               <mods:identifier type="doi">10.1039/D1DT00104C</mods:identifier>
               <mods:abstract>We report herein the synthesis, structural characterization and electrocatalytic properties of three new coordination&#xd;
polymers, resulting from the combination of divalent metal (Ca2+, Cd2+ or Co2+) salts with (2-carboxyethyl)(phenyl)phosphinic&#xd;
acid. In addition to the usual hydrothermal procedure, the Co2+ derivative could be also prepared by microwave-assisted&#xd;
synthesis, in much shorter times. The crystal structures were solved ab initio, from powder diffraction data. Compounds&#xd;
MII[O2P(CH2CH2COOH)(C6H5)]2 {M= Cd (1) or Ca (2)} crystallize in the monoclinic system and display a layered topology, with&#xd;
the phenyl groups pointing toward the interlayer space in a interdigitated fashion. Compound&#xd;
Co2[(O2P(CH2CH2COO)(C6H5)(H2O)]2·2H2O (3) presents a 1D structure composed of zig-zag chains, formed by edge-sharing&#xd;
cobalt octahedra, with phenyl groups pointing outside. Packing of these chains is favored by hydrogen bond interactions via&#xd;
lattice water. In addition, H-bonds along the chains are established with participation of the water molecules and the&#xd;
hydrophilic groups from the ligand. However, the solid exhibits a low proton conductivity, attributed to the isolation of the&#xd;
hydrophilic regions caused by the arrangement of hydrophobic phenyl groups. Preliminary studies on the electrocatalytical&#xd;
performance for the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) have been conducted for&#xd;
compound 3 and its pyrolytic derivatives, which were previously throughout characterized. By comparison, another Co2+&#xd;
phosphinate, 4, obtained by microwave-assisted synthesis, but with distinct stoichiometry and known structure was also&#xd;
tested. For OER, the best performance was reached with a derivative of 3, prepared by heating this compound in N2 at 200&#xd;
°C. This derivative presented overpotential (339 mV, for a current density of 10 mA·cm-2) and Tafel slope (51.7 mV·dec-1)&#xd;
values comparable to other Co2+ related materials.</mods:abstract>
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               <mods:subject>
                  <mods:topic>Electroquímica</mods:topic>
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               <mods:subject>
                  <mods:topic>Protones</mods:topic>
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               <mods:titleInfo>
                  <mods:title>Synthesis and Electrochemical properties of metal(II)- carboxyethylphenylphosphinates</mods:title>
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