4‐(Tert‐butylsulfanyl)‐2,6‐di(pyrazol‐1‐yl)pyridine (L) was obtained in low yield from a one‐pot reaction of 2,4,6‐trifluoropyridine with 2‐methylpropane‐2‐thiolate and sodium pyrazolate in a 1:1:2 ratio. The materials [FeL2][BF4]2·solv (1[BF4]2·solv) and [FeL2][ClO4]2·solv (1[ClO4]2·solv; solv = MeNO2, MeCN or Me2CO) exhibit a variety of structures and spin‐state behaviors including thermal spin‐crossover (SCO). Solvent loss on heating 1[BF4]2·xMeNO2 (x ≈ 2.3) occurs in two steps. The intermediate phase exhibits hysteretic SCO around 250 K, involving a “reverse‐SCO” step in its warming cycle at a scan rate of 5 Kmin‒1. The reverse‐SCO is not observed in a slower 1 Kmin‒1 measurement, however, confirming its kinetic nature. The final product [FeL2][BF4]2·0.75MeNO2 was crystallographically characterized, and shows abrupt but incomplete SCO at 172 K which correlates with disorder of an L ligand. The asymmetric unit of 1[BF4]2·yMe2CO (y ≈ 1.6) contains five unique complex molecules, four of which undergo gradual SCO in at least two discrete steps. Low‐spin 1[ClO4 ]2·0.5Me2CO is not isostructural with its BF4− congener, and undergoes single‐crystal‐to‐single‐crystal solvent loss with a tripling of the crystallographic unit cell volume, while retaining the P ‐1 space group. Three other solvate salts undergo gradual thermal SCO. Two of these are isomorphous at room temperature, but transform to different low‐temperature phases when the materials are fully low‐spin.
CORE (COnnecting REpositories)
CORE (COnnecting REpositories)