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Mn(dca)2(o-phen) {dca=dicyanamide; o-phen=1,10-phenanthroline}: Long-range magnetic order in a low-dimensional Mn-dca polymer
- Source :
-
Polyhedron . Mar2013, Vol. 52, p679-688. 10p. - Publication Year :
- 2013
-
Abstract
- Abstract: The crystal structure, phonon density-of-states, and magnetic properties of Mn(dca)2(o-phen) (dca=dicyanamide, N(CN)2 −; o-phen=1,10-phenanthroline) have been studied using several methods including magnetization, muon-spin relaxation, and neutron and X-ray scattering. From X-ray crystallography the structure was shown to consist of octahedral MnN6 sites that are connected via four μ1,5-bridging dca ligands while the two remaining cis-positions are occupied by N-donors of the o-phen ligand. Two Mn2+ ions are bridged together by two dca anions to afford [Mn2(dca)2(o-phen)2]2+ “dimers.” These dimers are linked in 2D via μ1,5-dca ligands to afford a polymeric structure whereas the o-phen ligands act as spacers. Bulk magnetic susceptibility data show a characteristic broad maximum at 2.65K while neutron scattering and muon-spin relaxation data establish T N =1.85K. For T ≪ T N, the magnetization, as obtained in pulsed-fields, saturates at 5.75T and reaches a moment typical of an isotropic S =5/2 ion. The magnetic structure was determined and found to consist of antiferromagnetically ordered Mn2+ moments oriented in the ac-plane with no spin-canting being evident. The magnetic space group symmetry for the Mn2+ moments is P21′/c with each Mn2+ ion carrying a magnetic moment of 4.7(1)μB, in good agreement with the value of 5.0μB expected for an isotropic, high-spin S =5/2 ion. The fact that LRO is observed in Mn(dca)2(o-phen) is unusual among low-dimensional dicyanamide complexes especially since only μ1,5-dca modes are involved. [Copyright &y& Elsevier]
Details
- Language :
- English
- ISSN :
- 02775387
- Volume :
- 52
- Database :
- Academic Search Index
- Journal :
- Polyhedron
- Publication Type :
- Academic Journal
- Accession number :
- 86397148
- Full Text :
- https://doi.org/10.1016/j.poly.2012.07.087