Formation of Layered Proton-Conducting Zirconium and Titanium Organophosphonates by Topotactic Reaction: Physicochemical Properties, Proton Dynamics, and Atomic-Resolution Structure

摘要

A series of new zirconium and titanium phosphates-organophosphonates, in which the organophosphonate moiety is functionalized with a sulfo group, was prepared by a topotactic reaction involving the gamma modification of zirconium or titanium hydrogen phosphate with 2-bis(phosphonomethypamino-ethan-l-sulfonic acid (H4TDP). H4TDP represents a new type of functionalizing agent, which can be easily prepared by a Moedritzer-Irani reaction from taurine (2-aminoethanesulfonic acid). The gamma modification of zirconium hydrogen phosphate (gamma-ZrP) with H4TDP provides mixed phosphateorganophosphonate compounds with the formula Zr(PO4)(H2PO4)(1-2x)(H2TDP)(x)center dot 7H(2)O, where x = 0.15, 0.34, 0.45, and is controlled by the gamma-ZrP/H4TDP ratio in the starting mixture. On the contrary, by the topotactic gamma modification of titanium hydrogen phosphate (gamma-TiP) with H4TDP, only one product with the formula Ti(PO4)(H2PO4)(1-z)(H2TDP)(z)center dot yH(2)O, where z = 0.41 +/- 0.01, was obtained regardless of the composition of the starting mixture. The synthesized compounds were characterized by elemental analysis, thermogravimetric analysis, energy-dispersive X-ray analysis, and infrared spectroscopy. The way the topotactic reaction proceeds and how the grafted organophosphonate groups are bonded to the layers of the host structure were suggested on the basis of the solid-state NMR data. It was found that the grafted moieties are spread evenly in the host layers among the hydrogen phosphate groups. The obtained solids are able to intercalate basic molecules, as was proved by the intercalation reactions of the zirconium series with butylamine. The amount of intercalated butylamine increases with increasing x. It is known that both host compounds, gamma-ZrP and gamma-TiP, are protonic conductors. It was found that the incorporation of H2TDP increases conductivity of the zirconium compound when x = 0.15, but further incorporation of H2TDP into the gamma-ZrP host structure leads to a decrease of conductivity. This behavior is explained on the basis of the H-1 MAS and the H-1-H-1 EXSY NMR data.