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

Abstract

Bistable spin-crossover (SCO) complexes that undergo abrupt and hysteretic (ΔT_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 ⋅CH₃ NO₂ (X=ClO₄ , 1; X=BF₄ , 2). Stable spin-state switching - T_1/2 =288 K; ΔT_1/2 =62 K - is observed for 1, whereas 2 undergoes above-room-temperature lattice-solvent content-dependent SCO - T_1/2 =331 K; ΔT_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.