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Poly[[tetraaquadi-μ(4)-oxalato-μ(2)-oxalato-dineodymium(III)] dihydrate]
The title compound, {[Nd(2)(C(2)O(4))(3)(H(2)O)(4)]·2H(2)O}(n), was synthesized hydrothermally in the presence of bis(carboxyethylgermanium) sesquioxide. It is isostructural with the corresponding Pr compound [Yang et al. (2009). Acta Cryst. E65, m1152–m1153]. The Nd(3+) cation is nine-coordina...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297245/ https://www.ncbi.nlm.nih.gov/pubmed/22412435 http://dx.doi.org/10.1107/S1600536812005016 |
Sumario: | The title compound, {[Nd(2)(C(2)O(4))(3)(H(2)O)(4)]·2H(2)O}(n), was synthesized hydrothermally in the presence of bis(carboxyethylgermanium) sesquioxide. It is isostructural with the corresponding Pr compound [Yang et al. (2009). Acta Cryst. E65, m1152–m1153]. The Nd(3+) cation is nine-coordinated and its coordination polyhedron can be described as a distorted tricapped trigonal prism. Two Nd(3+) ions are connected by two O atoms from two oxalate ions to give a dinuclear Nd(2) unit. The unit is further linked to four others via four oxalate ions yielding a layerparallel to (0-11). The linkages between the layers by neighbouring oxalate anions lead to a three-dimensional framework with channels along the c axis. The coordinating and free water molecules are located in the channels and make contact with each other and the host framework by weak O—H⋯O hydrogen bonds. |
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