Interplay between spin crossover and proton migration along short strong hydrogen bonds

Abstract

The iron(ii) salt [Fe(bpp)₂](isonicNO)₂·HisonicNO·5H₂O (<b>1</b>) (bpp = 2,6-bis(pyrazol-3-yl)pyridine; isonicNO = isonicotinate N-oxide anion) undergoes a partial spin crossover (SCO) with symmetry breaking at <i>T</i> ₁ = 167 K to a mixed-spin phase (50% high-spin (HS), 50% low-spin (LS)) that is metastable below <i>T</i> ₂ = 116 K. Annealing the compound at lower temperatures results in a 100% LS phase that differs from the initial HS phase in the formation of a hydrogen bond (HB) between two water molecules (O4W and O5W) of crystallisation. Neutron crystallography experiments have also evidenced a proton displacement inside a short strong hydrogen bond (SSHB) between two isonicNO anions. Both phenomena can also be detected in the mixed-spin phase. <b>1</b> undergoes a light-induced excited-state spin trapping (LIESST) of the 100% HS phase, with breaking of the O4W⋯O5W HB and the onset of proton static disorder in the SSHB, indicating the presence of a light-induced activation energy barrier for proton motion. This excited state shows a stepped relaxation at <i>T</i> ₁(LIESST) = 68 K and <i>T</i> ₂(LIESST) = 76 K. Photocrystallography measurements after the first relaxation step reveal a single Fe site with an intermediate geometry, resulting from the random distribution of the HS and LS sites throughout the lattice.