Issue 6, 2001

Spin frustration and concealed asymmetry: structure and magnetic spectrum of [Fe3O(O2CPh)6(py)3]ClO4·py

Abstract

The oxo-centred trinuclear complex [Fe3O(O2CPh)6(py)3]ClO4·py and its fully deuteriated analogue have been synthesized. X-Ray crystallography at T = 233 K shows that the complex has threefold symmetry, space group P63/m. Incoherent inelastic neutron scattering spectra at T = 1.5 K however show the presence of two inequivalent sets of molecules, one a static “isosceles” coupled system, with two J values for the three metal–metal interactions, the other a dynamic system, with rapid pseudorotation between equivalent isosceles geometries. Combining infrared and neutron scattering data, the distortion of the cluster has been estimated.

Graphical abstract: Spin frustration and concealed asymmetry: structure and magnetic spectrum of [Fe3O(O2CPh)6(py)3]ClO4·py [ ]

Supplementary files

Article information

Article type
Paper
Submitted
09 Oct 2000
Accepted
18 Jan 2001
First published
19 Feb 2001

J. Chem. Soc., Dalton Trans., 2001, 862-866

Spin frustration and concealed asymmetry: structure and magnetic spectrum of [Fe3O(O2CPh)6(py)3]ClO4·py

F. E. Sowrey, C. Tilford, S. Wocadlo, C. E. Anson, A. K. Powell, S. M. Bennington, W. Montfrooij, U. A. Jayasooriya and R. D. Cannon, J. Chem. Soc., Dalton Trans., 2001, 862 DOI: 10.1039/B008121N

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