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Bis(benzyl­tri­methyl­ammonium) bis­[(4SR,12SR,18RS,26RS)-4,18,26-trihy­droxy-12-oxido-13,17-dioxahepta­cyclo­[14.10.0.0(3,14).0(4,12).0(6,11).0(18,26).0(19,24)]hexa­cosa-1,3(14),6,8,10,15,19,21,23-nona­ene-5,25-dione] sesquihydrate: dimeric structure formation via [O—H—O](−) negative charge-assisted hydrogen bonds (–CAHB) with benzyl­tri­methyl­ammonium counter-ions

The reaction between bis-ninhydrin resorcinol and benzyl­tri­methyl­ammonium fluoride in ethanol has produced the title compound, 2C(10)H(16)N(+)·2C(24)H(13)O(8) (−)·1.5H(2)O, which contains a unique centrosymmetric supra­molecular dimeric entity, where two deprotonated ligands are held together via...

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Detalles Bibliográficos
Autores principales: Bengiat, Ravell, Gil, Maayan, Klein, Asne, Bogoslavsky, Benny, Cohen, Shmuel, Almog, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778823/
https://www.ncbi.nlm.nih.gov/pubmed/27006816
http://dx.doi.org/10.1107/S2056989016002899
Descripción
Sumario:The reaction between bis-ninhydrin resorcinol and benzyl­tri­methyl­ammonium fluoride in ethanol has produced the title compound, 2C(10)H(16)N(+)·2C(24)H(13)O(8) (−)·1.5H(2)O, which contains a unique centrosymmetric supra­molecular dimeric entity, where two deprotonated ligands are held together via two strong and short [O⋯O = 2.4395 (13) Å] [O—H—O](−) bonds of the type negative charge-assisted hydrogen bonds (–CAHB). The central aromatic rings of the ligands create parallel-displaced π–π stacking at an inter­planar distance of 3.381 (1) Å, which helps stabilize the dimer. In the crystal, two symmetry-related solvent water mol­ecules with a site occupancy of 0.75 are attached to the carbonyl groups of the dimer by weaker O—H⋯O hydrogen bonds, forming chains along [101].