dc.creatorRaffo, Pablo Alejandro
dc.creatorRossi, Leonardo
dc.creatorAlborés, Pablo
dc.creatorBaggio, Ricardo Fortunato
dc.creatorCukiernik, Fabio Daniel
dc.date.accessioned2017-12-27T20:04:34Z
dc.date.accessioned2018-11-06T14:59:37Z
dc.date.available2017-12-27T20:04:34Z
dc.date.available2018-11-06T14:59:37Z
dc.date.created2017-12-27T20:04:34Z
dc.date.issued2014-04
dc.identifierCukiernik, Fabio Daniel; Baggio, Ricardo Fortunato; Alborés, Pablo; Rossi, Leonardo; Raffo, Pablo Alejandro; Alkoxy-benzoic acids: Some lacking structures and rationalization of the molecular features governing their crystalline architectures; Elsevier Science; Journal of Molecular Structure; 1070; 4-2014; 86-93
dc.identifier0022-2860
dc.identifierhttp://hdl.handle.net/11336/31730
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1892583
dc.description.abstractThe crystalline structure of four alkoxy-substituted benzoic acids, namely 3-(methoxy)benzoic acid (I), (with two independent molecules in the asymmetric unit); 3,4-di(ethoxy)benzoic acid (II), 3,5-di(ethoxy)benzoic acid (III) and 3,4,5-tri(ethoxy)benzoic acid (IV) are presented, and the details of their packing arrangements discussed. In all cases the synthon is a H-bonded head-to-head dimer. C–H⋯π interactions involving C atoms at the 4-positions of neighbouring molecules organize the dimeric synthons in a perpendicular orientation in the case of I. These interactions being blocked for II, Van der Waals interchain interactions organise synthons therein in parallel orientation. In the case of III, although C–H⋯π interactions at the 4-positions are possible in principle, interchain interactions prevail, giving rise to a parallel arrangement of linear strands. Finally, compound IV with all three 3,4,5 substituted sites reduces its interaction scheme to stacking contacts, and the columns thus formed are essentially non interacting. An attempt to rationalize the molecular factors influencing the structures of the whole set of 3-, 4- and/or 5-methoxy- and ethoxy-substituted benzoic acids reported so far in the literature is performed.
dc.languageeng
dc.publisherElsevier Science
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.molstruc.2014.04.003
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0022286014003561
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectAlkoxy- substituted benzoic acids
dc.subjectPiPi and CHPi interactions
dc.subjectRationalization of packing modes
dc.titleAlkoxy-benzoic acids: Some lacking structures and rationalization of the molecular features governing their crystalline architectures
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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