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dc.contributor.authorMarushkevich, Kseniya
dc.contributor.authorKhriachtchev, Leonid
dc.contributor.authorRäsänen, Markku
dc.contributor.authorMelavuori, Mia
dc.contributor.authorLundell, Jan
dc.date.accessioned2012-09-18T06:03:37Z
dc.date.available2013-01-26T22:45:03Z
dc.date.issued2012
dc.identifier.citationMarushkevich, K., Khriachtchev, L., Räsänen, M., Melavuori, M., & Lundell, J. (2012). Dimers of the Higher-Energy Conformer of Formic Acid: Experimental Observation. <i>The Journal of Physical Chemistry A</i>, <i>116</i>(9), 2101-2108. <a href="https://doi.org/10.1021/jp209714e" target="_blank">https://doi.org/10.1021/jp209714e</a>
dc.identifier.otherCONVID_21559934
dc.identifier.otherTUTKAID_51592
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/38560
dc.description.abstractWe report on the first experimental observation of formic acid dimers composed of two molecules of the higher-energy cis conformer. The cis–cis formic acid dimers are prepared in an argon matrix by selective vibrational excitation of the ground state trans conformer (deuterated form HCOOD) combined with thermal annealing of the matrix at about 30 K. Five cis–cis formic acid dimers are predicted by ab initio calculations (interaction energies from −16.9 to −27.2 kJ molˉ¹), and these structures are used for the assignment of the experimental spectra. Selective vibrational excitation of the obtained cis–cis dimers leads to the formation of several trans–cis dimers, which supports the proposed assignments.fi
dc.language.isoeng
dc.publisherACS
dc.relation.ispartofseriesThe Journal of Physical Chemistry A
dc.subject.otherkonformeeri
dc.subject.otherIR spektroskopia
dc.subject.othervetysidos
dc.subject.otherconformer
dc.subject.otherIR spectroscopy
dc.subject.otherhydrogen bond
dc.titleDimers of the Higher-Energy Conformer of Formic Acid: Experimental Observation
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201208142141
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineKemiafi
dc.contributor.oppiaineChemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2012-08-14T03:30:06Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange2101-2108
dc.relation.issn1089-5639
dc.relation.numberinseries9
dc.relation.volume116
dc.type.versionpublishedVersion
dc.rights.copyright© ACS
dc.rights.accesslevelopenAccessfi
dc.subject.ysomuurahaishappo
jyx.subject.urihttp://www.yso.fi/onto/yso/p6513
dc.relation.doi10.1021/jp209714e
dc.type.okmA1


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