dc.creatorSaeed, Aamer
dc.creatorQasim, Muhammad
dc.creatorHussain, Majid
dc.creatorFlörke, Ulrich
dc.creatorErben, Mauricio Federico
dc.date2015
dc.date2020-10-23T17:01:13Z
dc.date.accessioned2023-07-14T22:53:57Z
dc.date.available2023-07-14T22:53:57Z
dc.identifierhttp://sedici.unlp.edu.ar/handle/10915/107627
dc.identifierissn:1386-1425
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/7448626
dc.descriptionThe tautomeric and conformational properties of a new tetrazole derivative are studied in a combined approach that includes the analysis of the experimental vibrational data together with theoretical calculation methods, especially in terms of natural bond orbital (NBO) population analysis. Moreover, the molecular and crystal structure was determined by single crystal X-ray diffraction. The compound crystallized as the 2-tautomeric form, monoclinic space group P21/c with Z = 4, a = 10.0630(14), b = 8.2879(11), c = 12.8375(18) Å, b = 105.546(3) , V = 1031.5(2) Å3. The tetrazole and phenyl rings are coplanar with the acetate group oriented perpendicular to the plane. The NBO analysis showed that delocalizing interactions of the lpp(N2) lone pair orbital contributes to a strong resonance interactions with both adjacent p⁄(N3@N4) and p⁄(N1@C5) antibonding orbitals of the tetrazole group.
dc.descriptionCentro de Química Inorgánica
dc.formatapplication/pdf
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rightsCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.subjectQuímica
dc.subjectTetrazole
dc.subjectVibrational spectroscopy
dc.subjectQuantum chemical calculations
dc.subjectCrystal structure
dc.subjectConformational analysis
dc.subjectTautomerism
dc.titleA combined experimental and theoretical study of the tautomeric and conformational properties of (5-phenyl-tetrazol-2-yl)-acetic acid methyl ester
dc.typeArticulo
dc.typeArticulo


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