Ordered and disordered solvates of C 60 and CBrCl 2 H
The formation of co-crystals is often unexpected; however, the Buckminster fullerene, for which many solvates are known,is an excellent system to study this tendency. In the present paper, C60 and CBrCl2H co-crystals have been studied. Hexagonal P6/mmmC60·2CBrCl2H co-crystals transform at 373 K to m...
| Autores: | , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2019 |
| País: | España |
| Institución: | Universitat Politècnica de Catalunya (UPC) |
| Repositorio: | UPCommons. Portal del coneixement obert de la UPC |
| Idioma: | inglés |
| OAI Identifier: | oai:upcommons.upc.edu:2117/175410 |
| Acceso en línea: | https://hdl.handle.net/2117/175410 https://dx.doi.org/10.1039/c8ce02150c |
| Access Level: | acceso abierto |
| Palabra clave: | Crystals Cristalls Àrees temàtiques de la UPC::Física::Física de l'estat sòlid::Cristalls |
| Sumario: | The formation of co-crystals is often unexpected; however, the Buckminster fullerene, for which many solvates are known,is an excellent system to study this tendency. In the present paper, C60 and CBrCl2H co-crystals have been studied. Hexagonal P6/mmmC60·2CBrCl2H co-crystals transform at 373 K to monoclinic C2/c C60·CBrCl2H co-crystals. While orientational disorder typical for C60 is found in the hexagonal co-crystals (as found in many C60 halomethane solvates), in the monoclinic co-crystals, C60 appears to be orientationally ordered. As for the solvent CBrCl2H, two types of occupational disorder involving the distribution of the halogen atoms can be observed, comparable to the behaviour in the two polymorphs of pure CBrCl2H. Within the monoclinic solvate, two sites are equally occupied by Br and Cl atoms (1/2:1/2), while one site is fully occupied by a Cl atom which leads to an average Cs symmetry for the solvent molecule. Whereas within the hexagonal co-crystals, each halogen position is occupied by 1/3:2/3 of Br or Cl atoms, respectively, leading to an average C3v molecular symmetry. The anisotropy of the intermolecular interactions coincides with the symmetry of the solvate structures and can be generalized for the C60·halomethane co-crystals. |
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