We probe, here, a family of 2D Hofmann-type frameworks, [Fe(Pd(CN))(bztrzX)]·HO [·HO; X = F, Cl, Br; = 1 (X = Cl, Br) and 3 (X = F); bztrzX = ()-1-(2-Xphen-1-yl)--(4-1,2,4-triazol-4-yl)methanimine], with halogen-appended ligands. In all cases, there are two crystallographically distinct Fe sites, ({Fe1-Fe2}), driven by the presence of a range of host-host and host-guest interactions. We find that lattice modification through X variation influences the elastic coupling between the Fe sites, the emergence of ferroelastic or antiferroelastic interactions between these sites, and the relative spin-state stabilization/destabilization at each site.
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