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Crystal structure of 4-(dimethylamino)pyridinium cis-diaquabis(oxalato-κ(2) O,O′)ferrate(III) hemihydrate
The Fe(III) ions in the hybrid title salt, (C(7)H(11)N(2))[Fe(C(2)O(4))(2)(H(2)O)(2)]·0.5H(2)O, show a distorted octahedral coordination environment, with four O atoms from two chelating oxalate dianions and two O atoms from two cis aqua ligands. The average Fe—O(oxalate) bond length [2.00 (2) Å] i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571360/ https://www.ncbi.nlm.nih.gov/pubmed/26396759 http://dx.doi.org/10.1107/S2056989015013213 |
Sumario: | The Fe(III) ions in the hybrid title salt, (C(7)H(11)N(2))[Fe(C(2)O(4))(2)(H(2)O)(2)]·0.5H(2)O, show a distorted octahedral coordination environment, with four O atoms from two chelating oxalate dianions and two O atoms from two cis aqua ligands. The average Fe—O(oxalate) bond length [2.00 (2) Å] is shorter than the average Fe—O(water) bond length [2.027 (19) Å]. The ionic components are connected via intermolecular N—H⋯O and O—H⋯O hydrogen bonds into a three-dimensional network. |
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