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dc.citation.endPage 1015 -
dc.citation.number 6045 -
dc.citation.startPage 1011 -
dc.citation.title SCIENCE -
dc.citation.volume 333 -
dc.contributor.author Schroeter, Christian -
dc.contributor.author Kosma, Kyriaki -
dc.contributor.author Schultz, Thomas -
dc.date.accessioned 2023-12-22T06:07:03Z -
dc.date.available 2023-12-22T06:07:03Z -
dc.date.created 2014-09-19 -
dc.date.issued 2011-08 -
dc.description.abstract Rotational spectra have traditionally been measured without a concurrent means of differentiating the molecular constituents of the sample. Here, we present an all-optical multipulse experiment that allows the correlated measurement of rotational and mass or photoelectron spectra by combining Fourier transform rotational coherence spectroscopy with resonance-enhanced multiphoton ionization. We demonstrate the power of this method with the determination of ground-state rotational constants and fragmentation channels for 10 different isotopes in a natural carbon disulfide sample. Three of the reported rotational constants were previously inaccessible by conventional spectroscopic techniques. -
dc.identifier.bibliographicCitation SCIENCE, v.333, no.6045, pp.1011 - 1015 -
dc.identifier.doi 10.1126/science.1204352 -
dc.identifier.issn 0036-8075 -
dc.identifier.scopusid 2-s2.0-80051890881 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/6234 -
dc.identifier.url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=80051890881 -
dc.identifier.wosid 000294000400054 -
dc.language 영어 -
dc.publisher AMER ASSOC ADVANCEMENT SCIENCE -
dc.title CRASY: Mass- or Electron-Correlated Rotational Alignment Spectroscopy -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -

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