A Reversible Hydrogen‐Bond Isomerization Triggered by an Abrupt Spin Crossover near Room Temperature
Verónica Jornet‐Mollá, Carlos Giménez‐Saiz, Dmitry S. Yufit, Judith A. K. Howard, Francisco M. Romero
Abstract
Abstract The spin crossover salt [Fe(bpp) 2 ](isonicNO) 2 ⋅ 2.4 H 2 O ( 1 ⋅2.4 H 2 O) (bpp=2,6‐bis(pyrazol‐3‐yl)pyridine; isonicNO=isonicotinate N ‐oxide anion) exhibits a very abrupt spin crossover at T 1 /2 =274.4 K. This triggers a supramolecular linkage (H‐bond) isomerization that responds reversibly towards light irradiation or temperature change. Isotopic effects in the thermomagnetic behavior reveal the importance of hydrogen bonds in defining the magnetic state. Further, the title compound can be reversibly dehydrated to afford 1 , a material that also exhibits spin crossover coupled to H‐bond isomerization, leading to strong kinetic effects in the thermomagnetic properties.