Crystallisation of H3BTC, H3TPO or H2SDA with MII (M = Co, Mn or Zn) and 2,2′-bipyridyl: Design and control of co-ordination architecture, and magnetic properties (H3BTC = benzene-1,3,5-tricarboxylic acid, H3TPO = tris(4-carboxylphenyl)phosphine oxide, H2SDA = cis-stilbene-4,4′-dicarboxylic acid)

M. John Plater*, Mark R.St J. Foreman, Eugenio Coronado, Carlos J. Gómez-Garcí, Alexandra M.Z. Slawin

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

134 Citations (Scopus)

Abstract

The hydrothermal reaction of benzene-1,3,5-tricarboxylic acid (H3BTC) with MII (M = Mn, Co or Zn), tris(4-carboxyphenyl)phosphine oxide (H3TPO) or cis-stilbene-4,4′-dicarboxylic acid (H2SDA) with CoII and 2,2′-bipyridyl (BIPY) gave 1-D co-ordination networks formulated as: [M(HBTC)(BIPY)(H2O)] (M = Mn 1, Co 2, or Zn 3; [Co3(BTC)2-(BIPY)2(H2O) 6]·4H2O 4, [Co3(TPO)2(BIPY)2(H2O) 6]·xH2O 5 and [Co(SDA)(BIPY)(H2O)] 6. Structures 1 and 2 consist of double stranded chains of alternating HBTC dianions and dimeric units MII-MII linked by two μ-(1,1) bridging carboxylates. Magnetic properties of 1 and 2 indicate the presence of ferromagnetic exchange interactions within the dimers. Structures 4 and 5 consist of chains with a molecular ladder motif which are stacked creating large channels lined by hydrated cobalt(II) ions. The H2O/D2O solvent exchange in structure 5, studied by infrared spectroscopy and thermal gravimetric analysis-mass spectrometry, provides evidence for the porosity and zeolitic nature of the material.

Original languageEnglish
Pages (from-to)4209-4216
Number of pages8
JournalJournal of the Chemical Society, Dalton Transactions
Issue number23
DOIs
Publication statusPublished - 7 Dec 1999

Bibliographical note

We are grateful to the Leverhulme Trust for financial support.

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