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      <dc:title>Proton conductivity of lanthanide nitrilotris-methylphosphonates</dc:title>
      <dc:creator>Salcedo, Inés R.</dc:creator>
      <dc:creator>Bazaga-García, Montse</dc:creator>
      <dc:creator>Pérez-Colodrero, Rosario Mercedes</dc:creator>
      <dc:creator>Olivera-Pastor, Pascual</dc:creator>
      <dc:creator>Losilla, Enrique R.</dc:creator>
      <dc:creator>Cabeza-Díaz, Aurelio</dc:creator>
      <dc:subject>Conductores orgánicos</dc:subject>
      <dc:description>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.</dc:description>
      <dc:date>2017-07-10T08:21:57Z</dc:date>
      <dc:date>2017-07-10T08:21:57Z</dc:date>
      <dc:date>2017</dc:date>
      <dc:date>2017-07-10</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>http://hdl.handle.net/10630/14157</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>XXXVI REUNIÓN BIENAL DE LA REAL SOCIEDAD ESPAÑOLA DE QUÍMICA</dc:relation>
      <dc:relation>Sitges, España</dc:relation>
      <dc:relation>25/06/2017 - 29/06/2017</dc:relation>
      <dc:rights>open access</dc:rights>
      <dc:rights>by-nc-nd</dc:rights>
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