Room-Temperature Spin Crossover in a Solution of Iron(II) Complexes with <i>N</i>,<i>N</i>′‑Disubstituted Bis(pyrazol-3-yl)pyridines

Here, we report a combined study of the effects of two chemical modifications to an N,N′-disubstituted bis­(pyrazol-3-yl)­pyridine (3-bpp) and of different solvents on the spin-crossover (SCO) behavior in otherwise high-spin iron­(II) complexes by solution NMR spectroscopy. The observed stabilization of the low-spin state by electron-withdrawing substituents in the two positions of the ligand that induce opposite electronic effects in SCO–active iron­(II) complexes of isomeric bis­(pyrazol-1-yl)­pyridines (1-bpp) was previously hidden by NH functionalities in 3-bpp precluding the molecular design of SCO compounds with this family of ligands. With the recent SCO-assisting substituent design, the uncovered trends converged toward the first iron­(II) complex of N,N′-disubstituted 3-bpp to undergo an almost complete SCO centered at room temperature in a less polar solvent of a high hydrogen-bond acceptor ability.