dc.citation.endPage |
1015 |
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dc.citation.number |
6045 |
- |
dc.citation.startPage |
1011 |
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dc.citation.title |
SCIENCE |
- |
dc.citation.volume |
333 |
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dc.contributor.author |
Schroeter, Christian |
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dc.contributor.author |
Kosma, Kyriaki |
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dc.contributor.author |
Schultz, Thomas |
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dc.date.accessioned |
2023-12-22T06:07:03Z |
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dc.date.available |
2023-12-22T06:07:03Z |
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dc.date.created |
2014-09-19 |
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dc.date.issued |
2011-08 |
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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. |
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dc.identifier.bibliographicCitation |
SCIENCE, v.333, no.6045, pp.1011 - 1015 |
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dc.identifier.doi |
10.1126/science.1204352 |
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dc.identifier.issn |
0036-8075 |
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dc.identifier.scopusid |
2-s2.0-80051890881 |
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dc.identifier.uri |
https://scholarworks.unist.ac.kr/handle/201301/6234 |
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dc.identifier.url |
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=80051890881 |
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dc.identifier.wosid |
000294000400054 |
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dc.language |
영어 |
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dc.publisher |
AMER ASSOC ADVANCEMENT SCIENCE |
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dc.title |
CRASY: Mass- or Electron-Correlated Rotational Alignment Spectroscopy |
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dc.type |
Article |
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dc.description.journalRegisteredClass |
scie |
- |
dc.description.journalRegisteredClass |
scopus |
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