The Black Polymorph of TTF-CA: TTF Polymorphism and Solvent Effects in Mechanochemical and Vapor Digestion Syntheses, FT-IR, Crystal Packing, and Electronic Structure
Résumé
Tetrathiafulvalene-chloranil (TTF-CA) was synthesized by two methods, liquid assisted grinding (LAG) and vapor digestion (VD), which largely reduce the use of reaction solvents. The effects of the small quantities of LAG solvent and solvent vapors in VD toward the formation of a particular TTF-CA product polymorph were studied from both tetrathiafulvalene forms (orange and brown) as reactants. It was concluded that a high solvent polarity index favors the formation of the ionic black polymorph of TTF-CA vs the quasi-neutral green form, whereas the crystal structure and crystal habit of the orange tetrathiafulvalene polymorph also favors the formation of the black TTF-CA. The crystal structure of the black TTF-CA was determined from synchrotron X-ray powder diffraction (XRPD), and it consists of dimerized TTF+center dot and CA(-center dot) radical ions, in agreement with room temperature magnetic susceptibility measurements indicating the material is diamagnetic. FT-IR showed that the compound is a semiconductor with a small. band gap of similar to 0.198 eV and it remains ionic at low temperatures. The latter was confirmed by XRPD showing the black TTF-CA does not undergo a phase transition in the range 298-20 K. Band structure calculations are in good agreement with the measured band gap.