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Diaqua­(5,10,15,20-tetra­phenyl­porphyrinato-κ(4) N)magnesium–18-crown-6 (1/1)

In the title compound, [Mg(C(44)H(28)N(4))(H(2)O)(2)]·C(12)H(24)O(6), the Mg(II) cation lies on an inversion center and is octa­hedrally coordinated by the four N atoms of the deprotonated tetra­phenyl­porphyrin (TPP) ligand and by two water mol­ecules. The asymmetric unit contains one half of the [...

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Detalles Bibliográficos
Autores principales: Ezzayani, Khaireddine, Nasri, Soumaya, Belkhiria, Mohamed Salah, Daran, Jean-Claude, Nasri, Habib
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569206/
https://www.ncbi.nlm.nih.gov/pubmed/23424408
http://dx.doi.org/10.1107/S1600536813001219
Descripción
Sumario:In the title compound, [Mg(C(44)H(28)N(4))(H(2)O)(2)]·C(12)H(24)O(6), the Mg(II) cation lies on an inversion center and is octa­hedrally coordinated by the four N atoms of the deprotonated tetra­phenyl­porphyrin (TPP) ligand and by two water mol­ecules. The asymmetric unit contains one half of the [Mg(TPP)(H(2)O)(2)] complex and one half of an 18-crown-6 mol­ecule. The average equatorial magnesium–pyrrole N atom distance (Mg—N(p)) is 2.071 (1) Å and the axial Mg—O(H(2)O) bond length is 2.213 (1) Å. The crystal packing is stabilized by two O—H⋯O hydrogen bonds between coordinating water mol­ecules and adjacent 18-crown-6 mol­ecules, and exhibits a one-dimensional supramolecular structure along the a axis. The supramolecular architecture is futher stabilized by weak C—H⋯π inter­actions. The 18-crown-6 mol­ecule is disordered over two sets of sites with an occupancy ratio of 0.8:0.2.