To disentangle the information contained in transition-metal
K-edge
X-ray magnetic circular dichroism (XMCD), two series of Prussian blue
analogs (PBAs) were investigated as model compounds. The number of
3d electrons and the magnetic orbitals have been varied on both sites
of the bimetallic cyanide polymer by combining with the hexacyanoferrate
or the hexacyanochromate entities’ various divalent metal ions
A2+ (Mn2+, Fe2+, Co2+,
Ni2+, and Cu2+). These PBA were studied by Fe
and Cr X-ray absorption spectroscopy and XMCD. The results, compared
to those obtained at the A K-edges in a previous work, show that transition-metal
K-edge XMCD is very sensitive to orbital symmetry and can therefore
give valuable information on the local structure of the magnetic centers.
Expressions of the intensity of the main 1s → 4p contribution
to the signal are proposed for all K-edges and all compounds. The
results pave the way toward a new tool for molecular materials able
to give access to valuable information on the local orientation of
the magnetic moments or to better understand the role of 4p orbitals
involved in their magnetic properties.