Abstract
AMX3 compounds are structurally diverse, a notable example being the post-perovskite structure which adopts a
two-dimensional framework with corner- and edge-sharing
octahedra. Few molecular post-perovskites are known and
of these, none have reported magnetic structures. Here
we report the synthesis, structure and magnetic properties
of molecular post-perovskites: CsNi(NCS)3, a thiocyanate
framework, and two new isostructural analogues
CsCo(NCS)3 and CsMn(NCS)3. Magnetisation measurements show that all three compounds undergo magnetic order. CsNi(NCS)3 (Curie temperature, TC = 8.5(1) K) and CsCo(NCS)3 (TC = 6.7(1) K) order as weak ferromagnets. On the other hand, CsMn(NCS)3 orders as an antiferromagnet (Néel temperature, TN = 16.8(8) K). Neutron diffraction data of CsNi(NCS)3 and CsMn(NCS)3, show that both are non-collinear magnets. These results suggest molecular frameworks are fruitful ground for realising the spin textures required for the next generation of information technology.
Supplementary materials
Title
Supplementary information
Description
Experimental details for synthesis, physical property measurements and computational calculations. Additional figures and crystallographic tables with refinement statistics.
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