Novel open-framework architectures in lanthanide phosphonates

J A Groves, N F Stephens, P A Wright, P Lightfoot

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31 Citations (Scopus)

Abstract

Two novel three-dimensional lanthanide coordination polymers have been prepared hydrothermally with the phosphortic acid N, N'-piperazine bis(methylenephosphonic acid), H2O3PCH2N(C2H4)(2)NCH2PO3H2 (LH4). The structures of Gd-2(LH2)(3)(.)3H(2)O (I) and Nd-2(LH2)(3)(.)9H(2)O (II) have been characterised by single crystal X-ray techniques. One-dimensional 'lanthanide-phosphate' chains are a key feature in both structures, although there are major structural differences between the chains, with (I) displaying octahedral GdO6 coordination and (II) showing eight-coordinate NdO8 polyhedra. In each case, three-dimensional connectivity is completed by coordination of the phosphonate group resulting in open framework structures encapsulating loosely bound water molecules. Isostructural Y3+ and Yb3+ analogues of (I) have been prepared, suggesting that cation size is a key factor in controlling the differing reaction products. In the case Of Y-2(LH2)(3)(.)5H(2)O, isostructural to (I), it is shown that the extra-framework water Molecules may be removed reversibly without framework collapse. Structural relationships to other known lanthanide phosphonates are discussed. (c) 2006 Elsevier SAS. All rights reserved.

Original languageEnglish
Pages (from-to)397-403
Number of pages7
JournalSolid State Sciences
Volume8
Issue number3-4
DOIs
Publication statusPublished - 2006

Keywords

  • HYDROTHERMAL SYNTHESIS
  • DIPHOSPHONATE
  • SILICATES
  • HYDROGEN
  • ACID

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