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Authordc.contributor.authorCampodónico, Paola R. 
Authordc.contributor.authorAizman, Arie es_CL
Authordc.contributor.authorContreras Ramos, Renato es_CL
Admission datedc.date.accessioned2008-12-15T16:06:34Z
Available datedc.date.available2008-12-15T16:06:34Z
Publication datedc.date.issued2006-04-28
Cita de ítemdc.identifier.citationCHEMICAL PHYSICS LETTERS Volume: 422 Issue: 1-3 Pages: 204-209 Published: APR 28 2006en
Identifierdc.identifier.issn0009-2614
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/118768
Abstractdc.description.abstractTwo classical tools, the intermolecular stretching force constants of H-bonded complexes and the molecular electrostatic potential are used to propose a nucleophilicity index evaluated for a series of pyridines. The model is validated against kinetic data recorded for the aminolysis of S-methyl 2,4-dinitrophenyl thiocarbonate.en
Lenguagedc.language.isoenen
Publisherdc.publisherELSEVIERen
Keywordsdc.subjectELECTROSTATIC PREDICTIONSen
Títulodc.titleEmpirical scale of nucleophilicity for substituted pyridinesen
Document typedc.typeArtículo de revista


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