Hydrothermal synthesis and characterisation of alkaline-earth metal salts of benzene-1,3,5-tricarboxylic acid

M. John Plater*, Alexander J. Roberts, Jim Marr, Eric E. Lachowski, R. Alan Howie

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

82 Citations (Scopus)

Abstract

The reaction of MII acetate (M = Sr or Ba) with benzene-1,3,5-tricarboxylic acid (H3btc) yielded crystals of formulae [M(Hbtc)(H2O)·0.5H2O. These compounds are isostructural as shown by X-ray single-crystal analysis and by X-ray powder diffraction patterns. The structures consist of alternating layers of parallel Hbtc anions and cations stacked along the c axis. The metal ions are co-ordinated by two bidentate carboxylate groups, three monodentate carboxylate groups and two water molecules giving an overall co-ordination number of nine. Heating liberates 2.5 water molecules per formulae unit to give M(Hbtc) which can reversibly bind water reforming [M(Hbtc)(H2O)2]·0.5H2O.

Original languageEnglish
Pages (from-to)797-802
Number of pages6
JournalJournal of the Chemical Society, Dalton Transactions
Issue number5
DOIs
Publication statusPublished - 7 Mar 1998

Bibliographical note

We are grateful to Professor F. P. Glasser for helpful discussions.

Fingerprint

Dive into the research topics of 'Hydrothermal synthesis and characterisation of alkaline-earth metal salts of benzene-1,3,5-tricarboxylic acid'. Together they form a unique fingerprint.

Cite this