Thermal spin-crossover with a large hysteresis spanning room temperature in a mononuclear complex.

A large hysteresis centered around room temperature represents one of the mandatory goals of research on functional switchable materials. In the thoroughly studied field of spin-crossover, such behaviour appears very rarely and essentially concerns coordination networks. A new compound showing a large spin-crossover hysteresis spanning room temperature demonstrates in a definitive manner that this goal is achievable in molecular discrete compounds without damaging the single-crystal character.

Structural movies of the gradual spin-crossover in a molecular complex at various physical scales.

The thermally induced Spin-CrossOver (SCO) undergone by the mononuclear iron(ii) complex [Fe(PM-AzA)2(NCS)2] (PM = N-2'-pyridylmethylene, AzA = 4-(phenylazo)aniline) is fully pictured by a quasi-continuous structural determination all along the spin-state modification within the sample. This large scale multi-temperature Single-Crystal X-Ray Diffraction (SCXRD) investigation leads to making structural movies. The latter reveal or confirm some features of the SCO that are subsequently validated by the same systematic investigation performed on a zinc isostructural analogue complex. Notably, the continuous views of the temperature dependencies of the unit-cell parameters, the dilatation tensors, the metal coordination sphere geometry and the intermolecular distances confirm a few of the structure-property relationships already known for SCO materials. In parallel, the examination of the temperature dependencies of the atomic coordinates and the atomic displacement parameters reveals unexpected behaviours in this gradual SCO material such as antagonistic atomic movements due to the single SCO and the pure thermal effects.

Surface-induced spin state locking of the [Fe(H2B(pz)2)2(bipy)] spin crossover complex.

Temperature- and coverage-dependent studies of the Au(1 1 1)-supported spin crossover Fe(II) complex (SCO) of the type [Fe(H2B(pz)2)2(bipy)] with a suite of surface-sensitive spectroscopy and microscopy tools show that the substrate inhibits thermally induced transitions of the molecular spin state, so that both high-spin and low-spin states are preserved far beyond the spin transition temperature of free molecules. Scanning tunneling microscopy confirms that [Fe(H2B(pz)2)2(bipy)] grows as ordered, molecular bilayer islands at sub-monolayer coverage and as disordered film at higher coverage. The temperature dependence of the electronic structure suggest that the SCO films exhibit a mixture of spin states at room temperature, but upon cooling below the spin crossover transition the film spin state is best described as a mix of high-spin and low-spin state molecules of a ratio that is constant. This locking of the spin state is most likely the result of a substrate-induced conformational change of the interfacial molecules, but it is estimated that also the intra-atomic electron-electron Coulomb correlation energy, or Hubbard correlation energy U, could be an additional contributing factor.

Activation of coherent lattice phonon following ultrafast molecular spin-state photo-switching: A molecule-to-lattice energy transfer.

We combine ultrafast optical spectroscopy with femtosecond X-ray absorption to study the photo-switching dynamics of the [Fe(PM-AzA)2(NCS)2] spin-crossover molecular solid. The light-induced excited spin-state trapping process switches the molecules from low spin to high spin (HS) states on the sub-picosecond timescale. The change of the electronic state (<50 fs) induces a structural reorganization of the molecule within 160 fs. This transformation is accompanied by coherent molecular vibrations in the HS potential and especially a rapidly damped Fe-ligand breathing mode. The time-resolved studies evidence a delayed activation of coherent optical phonons of the lattice surrounding the photoexcited molecules.