Show simple item record

ESR, electrochemical and cyclodextrin-inclusion studies of triazolopyridyl pyridyl ketones and dipyridyl ketones derivatives

Authordc.contributor.authorOlea Azar, Claudio 
Authordc.contributor.authorAbarca, B. es_CL
Authordc.contributor.authorNorambuena, Ester es_CL
Authordc.contributor.authorOpazo, L. es_CL
Authordc.contributor.authorJullian Matthaei, Carolina es_CL
Authordc.contributor.authorValencia, S. es_CL
Authordc.contributor.authorBallesteros, R. es_CL
Authordc.contributor.authorChadlaoui, M. 
Admission datedc.date.accessioned2010-01-07T17:43:31Z
Available datedc.date.available2010-01-07T17:43:31Z
Publication datedc.date.issued2008-11
Cita de ítemdc.identifier.citationSpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, Volume 71, Issue 2, 2008, Pages 703-709en_US
Identifierdc.identifier.issn1386-1425
Identifierdc.identifier.urihttp://repositorio.uchile.cl/handle/2250/120838
Abstractdc.description.abstractThe electron spin resonance (ESR) spectra of free radicals obtained by electrolytic reduction of triazolopyridyl pyridyl ketones and dipyridyl ketones derivatives were measured in dimethylsulfoxide (DMSO). The hyperfine patterns indicate that the spin density delocalization is dependent of the rings presented in the molecule. The electrochemistry of these compounds was characterized using cyclic voltammetry, in DMSO as solvent. When one carbonyl is present in the molecule one step in the reduction mechanism was observed while two carbonyl are present two steps were detected. The first wave was assigned to the generation of the correspondent free radical species, and the second wave was assigned to the dianion derivatives. The phase–solubility measurements indicated an interaction between molecules selected and cyclodextrins in water. These inclusion complexes are 1:1 with CD, and HP- CD. The values of Ks showed a different kind of complexes depending on which rings are included. AM1 and DFT calculations were performed to obtain the optimized geometries, theoretical hyperfine constants, and spin distributions, respectively. The theoretical results are in complete agreement with the experimental ones.en_US
Patrocinadordc.description.sponsorshipOur thanks are due to the Ministerio de Educaci´on y Ciencia Project CTQ 2006-15672-C05-03/BQC and Vicerrectorado de Relaciones Internacionales de la Universidad de Valencia for a grant to C.O.-A.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherElsevier B.V.en_US
Keywordsdc.subjectTriazolopyridyl pyridyl ketonesen_US
Títulodc.titleESR, electrochemical and cyclodextrin-inclusion studies of triazolopyridyl pyridyl ketones and dipyridyl ketones derivativesen_US
Document typedc.typeArtículo de revistaen_US


Files in this item

Icon

This item appears in the following Collection(s)

Show simple item record