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Structure and IR Spectra of 3(5)-Aminopyrazoles and UV-induced tautomerization in argon matrix

dc.contributor.authorSecrieru, Alina
dc.contributor.authorLopes, Susy
dc.contributor.authorCristiano, Maria L. S.
dc.contributor.authorFausto, Rui
dc.date.accessioned2021-07-29T09:11:57Z
dc.date.available2021-07-29T09:11:57Z
dc.date.issued2021-07-15
dc.date.updated2021-07-23T13:26:55Z
dc.description.abstractThe prototropic tautomerism in 3(5)-aminopyrazoles was investigated by matrix isolation infrared (IR) spectroscopy, supported by DFT(B3LYP)/6-311++G(d,p) calculations. In consonance with the experimental data, the calculations predict tautomer 3-aminopyrazole (3AP) to be more stable than the 5-aminopyrazole (5AP) tautomer (calculated energy difference: 10.7 kJ mol−1 ; Gibbs free energy difference: 9.8 kJ mol−1 ). The obtained matrix isolation IR spectra (in both argon and xenon matrices) were interpreted, and the observed bands were assigned to the tautomeric forms with help of vibrational calculations carried out at both harmonic and anharmonic levels. The matrix-isolated compound (in argon matrix) was then subjected to in situ broadband UV irradiation (λ > 235 nm), and the UV-induced transformations were followed by IR spectroscopy. Phototautomerization of the 3AP tautomer into the 5AP form was observed as the strongly prevalent reaction.pt_PT
dc.description.sponsorshipUI0313B/QUI/2020, UI0313P/QUI/2020pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifierdoi: 10.3390/molecules26144299
dc.identifier.citationMolecules 26 (14): 4299 (2021)pt_PT
dc.identifier.doi10.3390/molecules26144299pt_PT
dc.identifier.eissn1420-3049
dc.identifier.urihttp://hdl.handle.net/10400.1/16835
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherMDPIpt_PT
dc.relationCentre of Marine Sciences
dc.relationDevelopment of pyrazolopyrimidines as anti-tuberculosis agents – hit-to-lead optimization and chemical proteomic target identification.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subject3(5)-aminopyrazolept_PT
dc.subjectUV-induced phototautomerismpt_PT
dc.subjectMatrix isolationpt_PT
dc.subjectInfrared spectroscopypt_PT
dc.subjectDFT and TD-DFT calculationspt_PT
dc.subjectAnharmonic frequenciespt_PT
dc.titleStructure and IR Spectra of 3(5)-Aminopyrazoles and UV-induced tautomerization in argon matrixpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.awardTitleCentre of Marine Sciences
oaire.awardTitleDevelopment of pyrazolopyrimidines as anti-tuberculosis agents – hit-to-lead optimization and chemical proteomic target identification.
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FMulti%2F04326%2F2019/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/OE/SFRH%2FBD%2F140249%2F2018/PT
oaire.citation.issue14pt_PT
oaire.citation.startPage4299pt_PT
oaire.citation.titleMoleculespt_PT
oaire.citation.volume26pt_PT
oaire.fundingStream6817 - DCRRNI ID
oaire.fundingStreamOE
person.familyNameSecrieru
person.familyNameCristiano
person.givenNameAlina
person.givenNameMaria de Lurdes
person.identifier.ciencia-id0014-D52F-FF47
person.identifier.ciencia-idE411-6006-5A01
person.identifier.orcid0000-0002-9447-2855
person.identifier.ridG-2345-2012
person.identifier.scopus-author-id9238724800
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationdd633f1f-1a9f-41c5-bce7-72fe2c045c71
relation.isAuthorOfPublicationb16751a6-748e-44b0-9c59-058cbd5b2cc3
relation.isAuthorOfPublication.latestForDiscoveryb16751a6-748e-44b0-9c59-058cbd5b2cc3
relation.isProjectOfPublicationf38dbd9d-3734-4f3c-8d74-dff8dcaa8674
relation.isProjectOfPublication40e6e27f-5ebb-448d-b10e-329b19b8fcbc
relation.isProjectOfPublication.latestForDiscoveryf38dbd9d-3734-4f3c-8d74-dff8dcaa8674

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