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      <dc:title>Multifunctional lanthanum tetraphosphonates: Flexible, ultramicroporous and proton-conducting hybrid frameworks</dc:title>
      <dc:creator>Pérez-Colodrero, Rosario Mercedes</dc:creator>
      <dc:creator>Olivera-Pastor, Pascual</dc:creator>
      <dc:creator>Losilla, Enrique R.</dc:creator>
      <dc:creator>García-Aranda, Miguel Ángel</dc:creator>
      <dc:creator>León-Reina, Laura</dc:creator>
      <dc:creator>Papadaki, M.</dc:creator>
      <dc:creator>McKinlay, Alistair C.</dc:creator>
      <dc:creator>Morris, Russell E.</dc:creator>
      <dc:creator>Demadis, Konstantinos D.</dc:creator>
      <dc:creator>Cabeza-Díaz, Aurelio</dc:creator>
      <dc:subject>Química inorgánica</dc:subject>
      <dc:description>A new flexible ultramicroporous solid, La(H5DTMP)·7H2O (1), has been crystallized at room temperature using the tetraphosphonic acid H8DTMP, hexamethylenediamine-N,N,N′,N′-tetrakis(methylenephosphonic acid). Its crystal structure, solved by synchrotron powder X-ray diffraction, is characterised by a 3D pillared open-framework containing 1D channels filled with water. Upon dehydration, a new related crystalline phase, La(H5DTMP) (2) is formed. Partial rehydration of 2 led to La(H5DTMP)·2H2O (3). These new phases contain highly corrugated layers showing different degrees of conformational flexibility&#xd;
of the long organic chain. The combination of the structural study and the gas adsorption characterization (N2 and CO2) suggests an ultramicroporous flexible framework. NO isotherms are indicative of a strong irreversible adsorption of NO within the pores. Impedance data indicates that 1 is a proton-conductor with a conductivity of 8 × 10−3 S cm−1 at 297 K and 98% of relative humidity, and an activation energy of 0.25 eV.</dc:description>
      <dc:date>2021-03-08T08:34:10Z</dc:date>
      <dc:date>2021-03-08T08:34:10Z</dc:date>
      <dc:date>2012</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>Dalton Trans., 2012, 41, 4045–4051</dc:identifier>
      <dc:identifier>https://hdl.handle.net/10630/21039</dc:identifier>
      <dc:identifier>10.1039/c2dt11992g</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:rights>open access</dc:rights>
      <dc:publisher>The Royal Society of Chemistry</dc:publisher>
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