dc.creatorBerrueta Martinez, Yanina
dc.creatorRodriguez Pirani, Lucas Sebastian
dc.creatorErben, Mauricio Federico
dc.creatorBoese, Roland
dc.creatorReuter, Christian G.
dc.creatorVishnevskiy, Yury V.
dc.creatorMitzel, Norbert W.
dc.creatorDella Védova, Carlos Omar
dc.date.accessioned2018-06-12T20:09:54Z
dc.date.accessioned2018-11-06T13:28:58Z
dc.date.available2018-06-12T20:09:54Z
dc.date.available2018-11-06T13:28:58Z
dc.date.created2018-06-12T20:09:54Z
dc.date.issued2016-05
dc.identifierBerrueta Martinez, Yanina; Rodriguez Pirani, Lucas Sebastian; Erben, Mauricio Federico; Boese, Roland; Reuter, Christian G.; et al.; Structures of Trichloromethyl Thiocyanate, CCl 3 SCN, in Gaseous and Crystalline State; Wiley VCH Verlag; Chemphyschem; 17; 10; 5-2016; 1463-1467
dc.identifier1439-4235
dc.identifierhttp://hdl.handle.net/11336/48426
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1875851
dc.description.abstractTrichloromethyl thiocyanate, CCl3SCN, was structurally studied in both the gas and crystal phases by means of gas electron diffraction (GED) and single-crystal X-ray diffraction (XRD), respectively. Both experimental studies and quantum chemical calculations indicate a staggered orientation of the CCl3 group relative to the SCN group. This conclusion is supported by the similarity of the C-SCN bond length to that of the anti-structure of CH2ClSCN (Berrueta Martínez et al. Phys. Chem. Chem. Phys. 2015, 17, 15805-15812). Bond lengths and angles are similar for gas and crystal CCl3SCN structures; however, the crystal structure presents different intermolecular interactions. These include halogen and chalcogen type interactions, the geometry of which was studied. Characteristic C-Y⋯N angles (Y=Cl or S) close to 180° provide evidence for typical σ-hole interactions along the halogen/chalcogen-carbon bond in N⋯Cl and N⋯S, intermolecular units. Crystallize the difference: The crystal and gas-phase structures of CCl3SCN are studied by X-ray and gas electron diffraction techniques. In both phases, the CCl3 group presents a staggered orientation relative to the SCN group. Different intermolecular interactions are detected in the solid phase, including halogen- and chalcogen-type interactions.
dc.languageeng
dc.publisherWiley VCH Verlag
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1002/cphc.201600063
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/cphc.201600063
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectCHALCOGENS
dc.subjectCONFORMATION ANALYSIS
dc.subjectDENSITY FUNCTIONAL CALCULATIONS
dc.subjectHALOGENS
dc.subjectSOLID-STATE STRUCTURES
dc.titleStructures of Trichloromethyl Thiocyanate, CCl 3 SCN, in Gaseous and Crystalline State
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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