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dc.contributor.authorKosendiak, Iwona
dc.contributor.authorAhokas, Jussi M.E.
dc.contributor.authorKrupa, Justyna
dc.contributor.authorLundell, Jan
dc.contributor.authorWierzejewska, Maria
dc.date.accessioned2019-09-12T09:56:43Z
dc.date.available2019-09-12T09:56:43Z
dc.date.issued2019
dc.identifier.citationKosendiak, I., Ahokas, J. M., Krupa, J., Lundell, J., & Wierzejewska, M. (2019). Complexes of Glycolic Acid with Nitrogen Isolated in Argon Matrices. II : Vibrational Overtone Excitations. <i>Molecules</i>, <i>24</i>(18), Article 3245. <a href="https://doi.org/10.3390/molecules24183245" target="_blank">https://doi.org/10.3390/molecules24183245</a>
dc.identifier.otherCONVID_32813312
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/65487
dc.description.abstractStructural changes of glycolic acid (GA) complex with nitrogen induced by selective overtone excitation of the νOH mode were followed in argon matrices using FTIR spectroscopy. For the most stable SSC1 complex present in different trapping sites directly upon deposition site, selective changes in the νOH region were achieved upon near-infrared irradiation. Simultaneously, new conformers of the GA…N2 complex were formed, giving rise to several sets of bands in the νOH and νC=O regions of the spectra. Both position and intensity of new absorptions appeared to be highly sensitive on the wavelength of radiation used, as well as on the annealing of the matrix. Based on theoretical calculations at different levels of theory, an assignment of the observed bands is proposed and discussed.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesMolecules
dc.rightsCC BY 4.0
dc.subject.otherhydrogen bond
dc.subject.othermatrix isolation
dc.subject.othercarboxylic acid
dc.subject.othercomputational chemistry
dc.subject.othervibrational spectroscopy
dc.subject.othervibrational overtone
dc.titleComplexes of Glycolic Acid with Nitrogen Isolated in Argon Matrices. II : Vibrational Overtone Excitations
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201909124131
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineNanoscience Centerfi
dc.contributor.oppiaineKemiafi
dc.contributor.oppiaineFysikaalinen kemiafi
dc.contributor.oppiaineNanoscience Centeren
dc.contributor.oppiaineChemistryen
dc.contributor.oppiainePhysical Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn1420-3049
dc.relation.numberinseries18
dc.relation.volume24
dc.type.versionpublishedVersion
dc.rights.copyright© 2019 by the authors.
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber286844
dc.subject.ysolaskennallinen kemia
dc.subject.ysokarboksyylihapot
dc.subject.ysotyppi
dc.subject.ysovärähtelyt
dc.subject.ysovetysidokset
dc.subject.ysomolekyylit
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p23053
jyx.subject.urihttp://www.yso.fi/onto/yso/p27282
jyx.subject.urihttp://www.yso.fi/onto/yso/p10988
jyx.subject.urihttp://www.yso.fi/onto/yso/p708
jyx.subject.urihttp://www.yso.fi/onto/yso/p38131
jyx.subject.urihttp://www.yso.fi/onto/yso/p2984
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.3390/molecules24183245
dc.relation.funderSuomen Akatemiafi
dc.relation.funderResearch Council of Finlanden
jyx.fundingprogramAkatemiahanke, SAfi
jyx.fundingprogramAcademy Project, AoFen
jyx.fundinginformationThis research was funded by the National Science Centre Project No. 2013/11/B/ST4/00500 (at UWr to M.W.) and the Academy of Finland Project No. 286844 (at JYU to J.L.).
dc.type.okmA1


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