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dc.contributor.authorKuş, Nihal
dc.contributor.authorSharma, A.
dc.contributor.authorPena, I.
dc.contributor.authorBermudez, M. C.
dc.contributor.authorCabezas, C.
dc.contributor.authorAlonso, J. L.
dc.contributor.authorFausto, R.
dc.date.accessioned2019-10-20T09:13:32Z
dc.date.available2019-10-20T09:13:32Z
dc.date.issued2013
dc.identifier.issn0021-9606
dc.identifier.urihttps://dx.doi.org/10.1063/1.4799456
dc.identifier.urihttps://hdl.handle.net/11421/16954
dc.descriptionWOS: 000317788800014en_US
dc.descriptionPubMed ID: 24981533en_US
dc.description.abstractbeta-aminoisobutyric acid (BAIBA) has been studied in isolation conditions: in the gas phase and trapped into a cryogenic N-2 matrix. A solid sample of the compound was vaporized by laser ablation and investigated through their rotational spectra in a supersonic expansion using two different spectroscopic techniques: broadband chirped pulse Fourier transform microwave spectroscopy and conventional molecular beam Fourier transform microwave spectroscopy. Four conformers with structures of two types could be successfully identified by comparison of the experimental rotational and N-14 nuclear quadruple coupling constants with those predicted theoretically: type A, bearing an OH center dot center dot center dot N intramolecular hydrogen bond and its carboxylic group in the trans geometry (H-O-C=O dihedral similar to 180 degrees), and type B, having an NH center dot center dot center dot O bond and the cis arrangement of the carboxylic group. These two types of conformers could also be trapped from the gas phase into a cryogenic N-2 matrix and probed by Fourier transform infrared (IR) spectroscopy. In situ irradiation of BAIBA isolated in N-2 matrix of type B conformers using near-IR radiation tuned at the frequency of the O-H stretching 1st overtone (similar to 6930 cm(-1)) of these forms allowed to selectively convert them into type A conformers and into a new type of conformers of higher energy (type D) bearing an NH center dot center dot O=C bond and a O-H "free" trans carboxylic groupen_US
dc.description.sponsorshipCOMPETE-QREN-EU [PTDC/QUI-QUI/111879/2009]; Portugal-Spain Bilateral Project [E-7 CRUP-MCI 2011-E03]; Ministerio de Ciencia y Innovacion [CTQ 2006-05981/BQU, CTQ 2010-19008]; Consolider Ingenio [CSD 2009-00038]; Junta de Castilla y Leon [VA070A08]; Spain-Portugal Bilateral Project [AIB2010PT-00315]en_US
dc.description.sponsorshipThese studies were performed under projects PTDC/QUI-QUI/111879/2009 (also funded by COMPETE-QREN-EU) and the Portugal-Spain Bilateral Project E-7 CRUP-MCI 2011-E03. This work has also been supported by the Ministerio de Ciencia y Innovacion (Grant Nos. CTQ 2006-05981/BQU and CTQ 2010-19008), Consolider Ingenio 2010 (Grant No. CSD 2009-00038), Junta de Castilla y Leon (Grant No. VA070A08), and the Spain-Portugal Bilateral Project AIB2010PT-00315.en_US
dc.language.isoengen_US
dc.publisherAmer Inst Physicsen_US
dc.relation.isversionof10.1063/1.4799456en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleConformers of beta-aminoisobutyric acid probed by jet-cooled microwave and matrix isolation infrared spectroscopic techniquesen_US
dc.typearticleen_US
dc.relation.journalJournal of Chemical Physicsen_US
dc.contributor.departmentAnadolu Üniversitesi, Fen Fakültesi, Fizik Bölümüen_US
dc.identifier.volume138en_US
dc.identifier.issue14en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorKuş, Nihal


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