<?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>2026-05-27T16:25:44Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/14157" metadataPrefix="mods">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/14157</identifier><datestamp>2026-02-03T12:20:20Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</setSpec></header><metadata><mods:mods xmlns:doc="http://www.lyncode.com/xoai" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Salcedo, Inés R.</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Bazaga-García, Montse</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Pérez-Colodrero, Rosario Mercedes</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Olivera-Pastor, Pascual</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Losilla, Enrique R.</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Cabeza-Díaz, Aurelio</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2017-07-10T08:21:57Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2017-07-10T08:21:57Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2017-07-10</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="uri">http://hdl.handle.net/10630/14157</mods:identifier>
   <mods:abstract>Multifunctional metal phosphonates are acidic coordination polymers (CPs) with remarkable stability and proton conducting properties owing to their structure is usually composed of extended hydrogen-bond networks that favor proton transfer pathways [1].&#xd;
&#xd;
In this communication, three different families of proton conductors based on lanthanide nitrilotris-methylphosphonates are examined. Compounds were isolated by crystallization at room temperature at pH &lt;0.8 in the presence of. When chloride is presented in solution two families of compounds were isolated, depending on the concentration of chloride in solution: free-chloride 1D solids with formula Ln2(H3NMP)2(H2O)4]·4.5H2O [Ln= La3+] [2] or layered chloride-containing Ln(H4NMP)(H2O)2]Cl·2H2O [Ln= La3+ - Ho3+] materials [3]. In absence of chloride, a third series of compounds was obtained. This structural versatility leads to a wide range of proton conductivity varying between 3 × 10−4 S·cm−1 and 2 × 10−3 S·cm−1 as measured at 80 °C and 95% RH.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">by-nc-nd</mods:accessCondition>
   <mods:subject>
      <mods:topic>Conductores orgánicos</mods:topic>
   </mods:subject>
   <mods:titleInfo>
      <mods:title>Proton conductivity of lanthanide nitrilotris-methylphosphonates</mods:title>
   </mods:titleInfo>
   <mods:genre>conference output</mods:genre>
</mods:mods>
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