文摘
A quasielastic neutron scattering and solid-state 2H NMR spectroscopy study of the polymeric spin-crossover compound {Fe(pyrazine)[Pt(CN)b>4b>]} shows that the switching of the rotation of a molecular fragment鈥攖he pyrazine ligand鈥攐ccurs in association with the change of spin state. The rotation switching was examined on a wide time scale (10鈥?3鈥?0鈥? s) by both techniques, which clearly demonstrated the combination between molecular rotation and spin-crossover transition under external stimuli (temperature and chemical). The pyrazine rings are seen to perform a 4-fold jump motion about the coordinating nitrogen axis in the high-spin state. In the low-spin state, however, the motion is suppressed, while when the system incorporates benzene guest molecules, the movements of the system are even more restricted.