Please use this identifier to cite or link to this item:
https://apo.ansto.gov.au/dspace/handle/10238/6330
Title: | Switchable magnetism: neutron diffraction studies of the desolvated coordination polymer Co-3(OH)(2)(C4O4)(2) |
Authors: | Mole, RA Nadeem, MA Stride, JA Peterson, VK Wood, PT |
Keywords: | Neutron diffraction Polymers Magnetic properties Anisotropy Hamiltonians Cobalt |
Issue Date: | 13-Nov-2013 |
Publisher: | American Chemical Society |
Citation: | Mole, R. A., Nadeem, M. A., Stride, J. A., Peterson, V. K., & Wood, P. T. (2013). Switchable magnetism: neutron diffraction studies of the desolvated coordination polymer Co-3(OH)(2)(C4O4)(2). Inorganic Chemistry, 52(23), 13462-13468. doi:10.1021/ic4018344 |
Abstract: | We report the magnetic structure of the two magnetically ordered phases of Co3(OH)2(C4O4)2, a coordination polymer that consists of a triangular framework decorated with anisotropic Co(II) ions. Neutron diffraction experiments allow us to confirm that the magnetic behavior changes upon dehydration and reveal the complex phase behavior of this system, relative to the hydrated compound Co3(OH)2(C4O4)2·3H2O. One phase is shown to display spin idle behavior, where only a fraction of the moments order at intermediate temperatures, while at the lowest temperatures the system orders fully, in this case with a net magnetic moment. This novel magnetic behavior is discussed within the framework of a simple Hamiltonian and representational analysis and rationalizes this multiphase behavior by considering the combination of frustration and anisotropy. The change in behavior on dehydration is also rationalized with respect to the changes in the single-ion anisotropy of the cobalt. © 2013, American Chemical Society. |
Gov't Doc #: | 6179 |
URI: | http://dx.doi.org/10.1021/ic4018344 http://apo.ansto.gov.au/dspace/handle/10238/6330 |
ISSN: | 0002-7820 |
Appears in Collections: | Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.