Abstract
5-Acetyl-substituted pyrazole-3-carboxylic acid (H2L) forms [2 x 2] grid-like tetranuclear Cu(II) complexes with four five-coordinated copper(II) ions bridged by pyrazolate groups. Despite a significant dissociation of [Cu4L4(H2O)(4)]center dot 4H(2)O (1) in aqueous solution(1), it was possible to substitute the coordinated water molecules by pyridine ligands or azide anions. The resulting tetranuclear complexes [Cu4L4Py4]center dot 2H(2)O (2) and Na-4[Cu4L4(N-3)(4)]center dot 7MeOH (3) were isolated and studied by X-ray diffraction analysis. In 2 and 3 the azide anions or pyridine molecules complete the distorted square-pyramidal coordination of each copper(II) center. Magnetic susceptibilities of the obtained compounds have been measured by SQUID techniques. Simulation of the data using a Heisenberg spin Hamiltonian approach showed that the bridges between the metals mediate weak intramolecular antiferromagnetic coupling (J in the range -13.3 to -17.1 cm (1)) and lead to a singlet ground state in all cases. (C) 2012 Elsevier B.V. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 322-330 |
| Journal | Inorganica Chimica Acta |
| Volume | 392 |
| DOIs | |
| Publication status | Published - 2012 |
Bibliographical note
The information about affiliations in this record was updated in December 2015.The record was previously connected to the following departments: Chemical Physics (S) (011001060)
Subject classification (UKÄ)
- Atom and Molecular Physics and Optics
Free keywords
- Pyrazole ligands
- Copper(II)
- Grid complexes
- Magnetic properties
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