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Reorganization of intermolecular interactions in the polymorphic phase transition of a prototypical dithiazolyl-based bistable material
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The spin transitions undergone by several molecular crystals of dithiazolyl (DTA) radicals make this type of radicals promising candidates for future sensors and memory devices. Here, we present a systematic computational study of the intermolecular interactions existing in the two polymorphs of the neutral radical 1,3,5-trithia-2,4,6-triazapentalenyl in order to elucidate the origin of the difference in energy between those two polymorphs involved in its spin transition and to understand the crystal packing of this prototype of bistable materials. The π-π interactions between radicals are the main driving force for the crystal packing of both polymorphs, which comprises π-stacks of radicals. Among the interstack interactions, the strongest ones are those mediated by six- and four-center S···N bridges. The difference in energy between polymorphs, in turn, is mainly controlled also by the intrastack π-π intermolecular interactions, and the interstack S···S contacts instead of the S···N contacts. Since the supramolecular motifs herein identified as important for the crystal packing and/or for the energy difference between polymorphs (and, thus, for the spin transition temperature) are common to other members of the DTA family, our results provide valuable information to understand better the structure and properties of other switchable DTA-based materials.
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FRANCESE, Tommaso, MOTA VALERI, Fernando, DEUMAL I SOLÉ, Mercè, NOVOA VIDE, Juan j., HAVENITH, Remco w. a., BROER, Ria, RIBAS ARIÑO, Jordi. Reorganization of intermolecular interactions in the polymorphic phase transition of a prototypical dithiazolyl-based bistable material. _Crystal Growth & Design_. 2019. Vol. 19, núm. 4, pàgs. 2329-2339. [consulta: 31 de gener de 2026]. ISSN: 1528-7483. [Disponible a: https://hdl.handle.net/2445/154550]