Zeolitic imidazolate
frameworks (ZIFs) undergo pressure-induced
phase transitions that are peculiar to each ZIF. The phase transition
is associated with the rotation of the imidazolate, and it is accompanied
by an increase of their pore openings, affecting ZIFs performance
in separation processes. This phenomenon is known as the gate opening
or the swing effect. Here we report the metal dependence of the ambient
pressure and high pressure (HP) phases of ZIF-8(M) with M = Mg, Fe,
and Zn, determined by using periodic Kohn–Sham density functional
models. We show that the substitution of Zn with Mg or Fe has a big
influence on the gate opening energy, which significantly decreases,
an opposite trend than what was previously reported upon functionalization
of the linker. The lowest energy phase of ZIF-8(Fe) is different than
for ZIF-8(Mg) and ZIF-8(Zn), and its structure is significantly closer
to the HP phase. Multireference wave function methods have been used
to study the electronic structure of ZIF-8(Fe), confirming the metal
center to be high spin (S = 2) divalent iron in antiferromagnetic
coupling. The high-spin nature of the iron species coupled with a
band gap in the visible light range makes ZIF-8(Fe) an interesting
material for catalysis and photocatalysis.