Structural Insights into Hysteretic Spin-Crossover in a Set of Iron(II)-2,6-bis(1H-Pyrazol-1-yl)Pyridine) Complexes

Bistable spin-crossover (SCO) complexes that undergo abrupt and hysteretic (Delta T-1/2) spin-state switching are desirable for molecule-based switching and memory applications. In this study, we report on structural facets governing hysteretic SCO in a set of iron(II)-2,6-bis(1H-pyrazol-1-yl)pyridine) (bpp) complexes - [Fe(bpp-COOEt)(2)](X)(2).CH3NO2 (X=ClO4, 1; X=BF4, 2). Stable spin-state switching - T-1/2=288 K; Delta T-1/2=62 K - is observed for 1, whereas 2 undergoes above-room-temperature lattice-solvent content-dependent SCO - T-1/2=331 K; Delta T-1/2=43 K. Variable-temperature single-crystal X-ray diffraction studies of the complexes revealed pronounced molecular reorganizations - from the Jahn-Teller-distorted HS state to the less distorted LS state - and conformation switching of the ethyl group of the COOEt substituent upon SCO. Consequently, we propose that the large structural reorganizations rendered SCO hysteretic in 1 and 2. Such insights shedding light on the molecular origin of thermal hysteresis might enable the design of technologically relevant molecule-based switching and memory elements.

Automated summary

This study investigates the structural facets of bistable spin-crossover complexes and their role in inducing hysteresis. Through single-crystal X-ray diffraction studies, it is found that molecular reorganizations and conformation switching contribute to the observed spin-state switching and hysteresis. These insights could potentially aid in the design of molecule-based switching and memory elements.