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Crystal structures of two isotypic lanthanide(III) complexes: triaqua[2,6-diacetylpyridine bis(benzoylhydrazone)]methanollanthanide(III) trichloride methanol disolvates (Ln (III) = Tb and Dy)
The title lanthanide complexes, [Ln(DAPBH(2))(CH(3)OH)(H(2)O)(3)]Cl(3)·2CH(3)OH [Ln (III) = Tb and Dy; DAPBH(2) = 2,6-diacetylpyridine bis(benzoylhydrazone), C(23)H(21)N(5)O(2)], are isotypic. The central lanthanide ions are nine-coordinate, being ligated by three N and two O atoms from the pent...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5946983/ https://www.ncbi.nlm.nih.gov/pubmed/29765761 http://dx.doi.org/10.1107/S2056989018004103 |
Sumario: | The title lanthanide complexes, [Ln(DAPBH(2))(CH(3)OH)(H(2)O)(3)]Cl(3)·2CH(3)OH [Ln (III) = Tb and Dy; DAPBH(2) = 2,6-diacetylpyridine bis(benzoylhydrazone), C(23)H(21)N(5)O(2)], are isotypic. The central lanthanide ions are nine-coordinate, being ligated by three N and two O atoms from the pentadentate DAPBH(2) ligand, and four O atoms from the coordinated methanol molecule and three coordinated water molecules. The coordination geometry of the lanthanide ion is a distorted capped square antiprism. In the crystals, the various components are linked by O—H⋯Cl, N—H⋯Cl and O—H⋯O hydrogen bonds, forming three-dimensional supramolecular frameworks. Within the frameworks, there are C—H⋯Cl and C—H⋯O hydrogen bonds and offset π–π interactions (intercentroid distance ca 3.81 Å). |
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