Novel open-framework architectures in lanthanide phosphonates

被引:29
作者
Groves, JA [1 ]
Stephens, NF [1 ]
Wright, PA [1 ]
Lightfoot, P [1 ]
机构
[1] Univ St Andrews, Sch Chem, EaStChem, St Andrews KY16 9ST, Fife, Scotland
关键词
D O I
10.1016/j.solidstatesciences.2006.02.018
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
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.
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页码:397 / 403
页数:7
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