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dc.contributor.authorPérez, Cristóbal
dc.contributor.authorMata López, Santiago
dc.contributor.authorCabezas, Carlos
dc.contributor.authorLópez, Juan Carlos
dc.contributor.authorAlonso Hernández, José Luis 
dc.date.accessioned2017-03-20T12:58:46Z
dc.date.available2017-03-20T12:58:46Z
dc.date.issued2015
dc.identifier.citationJournal of Physical Chemistry A, 2015, 119 (16), pp 3731–3735es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/22665
dc.descriptionProducción Científicaes
dc.description.abstractIn this work neutral tyrosine has been generated in the gas phase by laser ablation of solid samples, and its most abundant conformers characterized through their rotational spectra. Their identification has been made by comparison between the experimental and ab initio values of the rotational and quadrupole coupling constants. Both conformers are stabilized by an O–H•••N hydrogen bond established within the amino acid skeleton chain and an additional weak N–H•••π hydrogen bond. The observed conformers differ in the orientation of the phenolic −OH group.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherAmerican Chemical Societyes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.classificationTirosinaes
dc.titleThe Rotational Spectrum of Tyrosinees
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© American Chemical Societyes
dc.identifier.doi10.1021/acs.jpca.5b01792es
dc.relation.publisherversionhttp://pubs.acs.orges
dc.identifier.publicationtitleJournal of Physical Chemistry Aes
dc.peerreviewedSIes
dc.description.projectJunta de Castilla y León (programa de apoyo a proyectos de investigación – Ref. VA175U13)es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International


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