The title salt, C2H8N+·C10H5O8−, was the unexpected product of an attempt to prepare a ZrIV metal–organic framework with benzene-1,2,4,5-tetracarboxylic acid (1,2,4,5-H3B4C). In the reaction, the DMF solvent has been decarbonylated, forming the dimethylammonium cation, with one proton lost from the tetracarboxylic acid. It is proposed that the ZrIV salt acts as a Tsotsi or robber, plundering CO from the DMF molecule. The resulting salt crystallizes with two cations and two anions in the asymmetric unit. An intramolecular hydrogen bond forms between a carboxylic acid substituent and the carboxylate group of each of the monodeprotonated (1,2,4,5-H3B4C−) anions. In the crystal, an extensive array of O—H...O, N—H...O and C—H...O hydrogen bonds generates a three-dimensional network, with columns of cations and anions forming along the b axis.
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Document Type: Research Article
Department of Chemistry, Rhodes University, PO Box 94, Grahamstown, South Africa
Department of Chemistry, Nelson Mandela University, Summerstrand, PO Box 77000, South Africa
January 1, 2016