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 language | English |
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Pages (from-to) | 397-403 |
Number of pages | 7 |
Journal | Solid State Sciences |
Volume | 8 |
Issue number | 3-4 |
DOIs | |
Publication status | Published - 2006 |
Keywords
- HYDROTHERMAL SYNTHESIS
- DIPHOSPHONATE
- SILICATES
- HYDROGEN
- ACID