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Tris(piperazinediium) bis[tris(pyridine-2,6-dicarboxylato)neodymate(III)] 15.33-hydrate
The title compound, (C(4)H(12)N(2))(3)[Nd(C(7)H(3)NO(4))(3)](2)·15.33H(2)O or (pipzH(2))(3)[Nd(pydc)(3)](2)·15.33H(2)O (in which pipz is piperazine and pydcH(2) is pyridine-2,6-dicarboxylic acid), was synthesized by the reaction of NdCl(3)·6H(2)O with the proton-transfer compound (pipzH(2))(pydc) in...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960278/ https://www.ncbi.nlm.nih.gov/pubmed/21201311 http://dx.doi.org/10.1107/S1600536807068328 |
Sumario: | The title compound, (C(4)H(12)N(2))(3)[Nd(C(7)H(3)NO(4))(3)](2)·15.33H(2)O or (pipzH(2))(3)[Nd(pydc)(3)](2)·15.33H(2)O (in which pipz is piperazine and pydcH(2) is pyridine-2,6-dicarboxylic acid), was synthesized by the reaction of NdCl(3)·6H(2)O with the proton-transfer compound (pipzH(2))(pydc) in aqueous solution. The nine donor atoms of the three pydc(2−) ligands form a distorted tricapped trigonal–prismatic arrangement around the Nd(III) center. Considerable C—O⋯π stacking interactions between CO groups of carboxylate fragments and aromatic rings of pydc(2−) with distances of 3.135 (5)–3.255 (5) Å are observed. In the crystal structure, a wide range of hydrogen-bonding [of the types O—H⋯O, N—H⋯O and C—H⋯O, with D⋯A distances ranging from 2.608 (10) to 3.278 (7) Å], ion-pairing and C—O⋯π stacking interactions connect the various components into a supramolecular structure. There is a high degree of solvent disorder in the structure; the occupancies of five water molecules refined to 0.6, 0.5, 0.4, 0.25 and 0.25. |
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