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Authordc.contributor.authorBenavente, E. 
Authordc.contributor.authorDíaz, C 
Authordc.contributor.authorGonzález, G 
Admission datedc.date.accessioned2018-12-20T15:13:09Z
Available datedc.date.available2018-12-20T15:13:09Z
Publication datedc.date.issued1992
Cita de ítemdc.identifier.citationPhosphorus, Sulfur, and Silicon and the Related Elements, Volumen 66, Issue 1-4, 1992, Pages 251-256
Identifierdc.identifier.issn15635325
Identifierdc.identifier.issn10426507
Identifierdc.identifier.other10.1080/10426509208038353
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/158526
Abstractdc.description.abstractThe influence of various common basic solvents on the IR and 1H-NMR spectra of a series of N,N′-thiodianilines, , X = H, OMe, Br, Cl, and m-NO2 has been studied. The solvent shifts of both, frequencies θ(NH) and chemical shifts δ(NH), show a near linear dependence on solvent basicity, DN (DN: Donor Number). The sensitivity of the thiodianilines to the solvent, expressed as the slopes in the curves δ(NH) and θ(NH) vs. DN, are determined by the inductive effect of the substituents on the amino group. The anomalous behavior of the m-NO2 derivative is attributed to strong intermolecular interactions.
Lenguagedc.language.isoen
Sourcedc.sourcePhosphorus, Sulfur, and Silicon and the Related Elements
Keywordsdc.subjectIR and IH-NMR spectra
Keywordsdc.subjectN, N′-Thiodianilines
Keywordsdc.subjectSolvent effect
Keywordsdc.subjectSulfur (II) compounds
Keywordsdc.subjectThionitrosobenzene precursors
Títulodc.titleSolvent effects on the infrared and 1h-nmr spectra of n, n'-thiodianilines
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso a solo metadatos
Catalogueruchile.catalogadorrvh
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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