Magnetic properties and molecular structure of complexes of substituted pyrazine ligands co-ordinated to iron(II) and copper(II) low dimensional antiferromagnetic interactions in diaquabis(pyrazinecarboxylato)iron(II)
- 1 January 1982
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in J. Chem. Soc., Dalton Trans.
- No. 12,p. 2419-2423
- https://doi.org/10.1039/dt9820002419
Abstract
The preparation and magnetic properties at 6–300 K are reported for the complexes [FeL2(H2O)2], [Fe(HL′)2]·3H2O, and [Cu(HL′)2]·3H2O, where HL = pyrazinecarboxylic acid and H2L′= 2,3-pyrazinedicarboxylic acid. The crystal structure of the compound [FeL2(H2O)2] is reported; it crystallizes as a monomer but the crystalline lattice contains an extensive network of hydrogen bonding with the hydrogen bonding along one direction shorter than in other directions. The magnetic data for [FeL2(H2O)2] exhibit a maximum in the temperature-dependent magnetic susceptibility at around 15 K, consistent with the Fisher linear-chain model (J/k=–1.3 K). The complex [Cu(HL′)2]·3H2O exhibits no magnetic interaction, whilst [Fe(HL′)2]·3H2O shows a low-temperature drop in the effective magnetic moment consistent with a zero-field splitting of the spin S= 2 multiplet (D/k= 12.6 K). Crystal data for [FeL2(H2O)2] : space group P21/c, Z= 2, a= 5.238(2), b= 11.198(2), c= 10.337(3)Å, β= 100.74(5)°, R= 0.077 for 604 reflections.Keywords
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