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Authordc.contributor.authorGonzález Moraga, Guillermo 
Authordc.contributor.authorChávez, Ivonne es_CL
Admission datedc.date.accessioned2014-06-03T14:44:53Z
Available datedc.date.available2014-06-03T14:44:53Z
Publication datedc.date.issued1981
Cita de ítemdc.identifier.citationJ. Chem. Soc, Faraday Trans. 2, 1981, 77, 2231-2236en_US
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/119794
Abstractdc.description.abstractAf-methylacetamide and acetamide has been studied. The chemical shifts at infinite dilution show approximately linear relationships with the donor number of the solvent. In strong donor solvents it is possible to observe the n.m.r. signáis of two non-equivalerit amidic protons in acetamide owing to the eftect of the solvent on C—N rotation. The influence of the solvent on the chemical shifts and line splittings is discussed as well as the concentration effects by considering possible solute-solvent and solute-solute interactions.en_US
Patrocinadordc.description.sponsorship"Servicio de Desarrollo Científico" of the University (Grant Q 546 813 4)en_US
Lenguagedc.language.isoenen_US
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Títulodc.titleSolvent Effects on the Amidic Bond: 1H Nuclear Magnetic Resonance Study of Acetamide and JV-Methylacetamideen_US
Document typedc.typeArtículo de revista


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile