A dihydrogen phosphate anionic network as a host lattice for cations in 1-methylpiperazine-1,4-diium bis(dihydrogen phosphate) and 2-(pyridin-2-yl)pyridinium dihydrogen phosphate-orthophosphoric acid (1/1).

Abstract

In the salt 1-methylpiperazine-1,4-diium bis(dihydrogen phosphate), C5H13N2(2+)·2H2PO4(-), (I), and the solvated salt 2-(pyridin-2-yl)pyridinium dihydrogen phosphate-orthophosphoric acid (1/1), C10H9N2(+)·H2PO4(-)·H3PO4, (II), the formation of O-H...O and N-H...O hydrogen bonds between the dihydrogen phosphate (H2PO4(-)) anions and the cations constructs a three- and two-dimensional anionic-cationic network, respectively. In (I), the self-assembly of H2PO4(-) anions forms a two-dimensional pseudo-honeycomb-like supramolecular architecture along the (010) plane. 1-Methylpiperazine-1,4-diium cations are trapped between the (010) anionic layers through three N-H...O hydrogen bonds. In solvated salt (II), the self-assembly of H2PO4(-) anions forms a two-dimensional supramolecular architecture with open channels projecting along the [001] direction. The 2-(pyridin-2-yl)pyridinium cations are trapped between the open channels by N-H...O and C-H...O hydrogen bonds. From a study of previously reported structures, dihydrogen phosphate anions show a supramolecular flexibility depending on the nature of the cations. The dihydrogen phosphate anion may be suitable for the design of the host lattice for host-guest supramolecular systems.