dc.creatorFaglioni, F.
dc.creatorLigabue, A.
dc.creatorPelloni, Stefano
dc.creatorSoncini, A.
dc.creatorViglione, R.G.
dc.creatorFerraro, Marta Beatriz
dc.creatorZanasi, R.
dc.creatorLazzeretti, Paolo
dc.date.accessioned2019-04-05T15:58:10Z
dc.date.accessioned2022-10-15T06:33:41Z
dc.date.available2019-04-05T15:58:10Z
dc.date.available2022-10-15T06:33:41Z
dc.date.created2019-04-05T15:58:10Z
dc.date.issued2005-12
dc.identifierFaglioni, F.; Ligabue, A.; Pelloni, Stefano; Soncini, A.; Viglione, R.G.; et al.; Why downfield proton chemical shifts are not reliable aromaticity indicators; American Chemical Society; Organic Letters; 7; 16; 12-2005; 3457-3460
dc.identifier1523-7060
dc.identifierhttp://hdl.handle.net/11336/73279
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4355769
dc.description.abstract(Chemical Equation Presented) Traces of magnetizability, traces of magnetic shielding at the hydrogen nuclei, and nucleus-independent chemical shift are not reliable aromaticity quantifiers for planar conjugated hydrocarbons. A measure of aromaticity is provided by the out-of-plane tensor components, whose magnitude is influenced by the π-ring currents. The failure of nucleus-independent chemical shift in this regard was proved for the molecule shown in the abstract graphic, sustaining a diatropic π-current. The validity of the ring-current model is reaffirmed.
dc.languageeng
dc.publisherAmerican Chemical Society
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/ol051103v
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/ol051103v
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.titleWhy downfield proton chemical shifts are not reliable aromaticity indicators
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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