<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-06T04:50:44Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/34460" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/34460</identifier><datestamp>2026-02-03T11:07:36Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
   <leader>00925njm 22002777a 4500</leader>
   <datafield ind2=" " ind1=" " tag="042">
      <subfield code="a">dc</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Salcedo, Inés R.</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Bazaga-García, Montse</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Pérez-Colodrero, Rosario Mercedes</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Vílchez-Cózar, Álvaro</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Cañamero-Cebrián, Fernando</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Olivera-Pastor, Pascual</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Zareba, Jan K.</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Cabeza-Díaz, Aurelio</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2024</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="520">
      <subfield code="a">Metal phosphonate-carboxylate compounds repre-sent a promising class of materials for proton conductionapplications. This study investigates the structural, thermal, andproton conduction properties of three groups of lanthanide-basedcompounds derived from 5-(dihydroxyphosphoryl)isophthalic acid(PiPhtA). The crystal structures, solved ab initio from X-raypowder diffraction data, reveal that groups Ln-I, Ln[O3P−C6H3(COO)(COOH)(H2O)2] (Ln = La, Pr), and Ln-II,Ln2{[O3P−C6H3(COO)(COOH)]2(H2O)4}·2H2O (Ln = La, Pr,Eu), exhibit three-dimensional frameworks, while group Ln-III,Ln[O3P−C6H3(COO)(COOH)(H2O)] (Ln = Yb), adopts alayered structure with unbonded carboxylic groups orientedtoward the interlayer region. All compounds feature carboxylicgroups and coordinating water molecules. Impedance measurements demonstrate that these materials exhibit water-mediated protonconductivity, initially following a vehicle-type proton-transfer mechanism. Upon exposure to ammonia vapors from a 14 or 28%aqueous solution, compounds from groups II and III adsorb ammonia and water, leading to an enhancement in proton conductivityconsistent with a Grotthuss-type proton-transfer mechanism. Notably, group II of the studied compounds undergoes the formationof a new expanded phase through the internal reaction of carboxylic groups with ammonia, coexisting with the as-synthesized phase.This postsynthetic modification results in a significant increase in proton conductivity, from approximately ∼5 × 10−6 to ∼10−4 S·cm−1 at 80 °C and 95% relative humidity (RH), attributed to a mixed intrinsic/extrinsic contribution. Remarkably, the NH3(28%)-exposed Yb-III compound achieves an enhancement in proton conductivity, reaching ∼ 5 × 10−3 S·cm−1 at 80 °C and 95% RH,primarily through an extrinsic contribution</subfield>
   </datafield>
   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">Inés R. Salcedo, Montse Bazaga-García, Rosario M. Pérez Colodrero, Álvaro Vílchez-Cózar, Fernando Cañamero-Cebrián, Pascual Olivera Pastor, Jan K. Zaręba, and Aurelio Cabeza. Structural Landscape and Proton Conduction of Lanthanide 5-(Dihydroxyphosphoryl)isophthalates. Crystal Growth &amp; Design 2024 24 (19), 7910-7918 DOI: 10.1021/acs.cgd.4c00786</subfield>
   </datafield>
   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">https://hdl.handle.net/10630/34460</subfield>
   </datafield>
   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">https://doi.org/10.1021/acs.cgd.4c00786</subfield>
   </datafield>
   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Química inorgánica</subfield>
   </datafield>
   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Protones</subfield>
   </datafield>
   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Conductividad</subfield>
   </datafield>
   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Iones</subfield>
   </datafield>
   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Structural Landscape and Proton Conduction of Lanthanide 5-(Dihydroxyphosphoryl)isophthalates</subfield>
   </datafield>
</record>
</metadata></record></GetRecord></OAI-PMH>