dc.citation.endPage |
755 |
- |
dc.citation.number |
5 |
- |
dc.citation.startPage |
751 |
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dc.citation.title |
CHEMPHYSCHEM |
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dc.citation.volume |
8 |
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dc.contributor.author |
Nolting, Dirk |
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dc.contributor.author |
Weinkauf, Rainer |
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dc.contributor.author |
Hertel, I.V. |
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dc.contributor.author |
Schultz, Thomas |
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dc.date.accessioned |
2023-12-22T09:36:12Z |
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dc.date.available |
2023-12-22T09:36:12Z |
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dc.date.created |
2014-09-19 |
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dc.date.issued |
2007-04 |
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dc.description.abstract |
The excited state dynamics of protonated adenine in the gas phase were investigated by femtosecond pump-probe transient mass spectroscopy. Adenine was protonated in an electrosproy ionization source and transferred to a Paul trap. Two femtosecond laser pulses at 266 nm and 800 nm excited the lowest electronic pi pi* state and probed the excited-state dynamics by monitoring ion fragment formation. The measured excited state decay is monoexponential with a lifetime shorter than 161 fs. This agrees with a theoretical prediction of very fast internal conversion via a conical intersection with the ground state. |
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dc.identifier.bibliographicCitation |
CHEMPHYSCHEM, v.8, no.5, pp.751 - 755 |
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dc.identifier.doi |
10.1002/cphc.200600727 |
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dc.identifier.issn |
1439-4235 |
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dc.identifier.scopusid |
2-s2.0-34247358160 |
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dc.identifier.uri |
https://scholarworks.unist.ac.kr/handle/201301/6255 |
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dc.identifier.url |
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=34247358160 |
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dc.identifier.wosid |
000245683400017 |
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dc.language |
영어 |
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dc.publisher |
WILEY-V C H VERLAG GMBH |
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dc.title |
Excited-state relaxation of protonated adenine |
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dc.type |
Article |
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dc.description.journalRegisteredClass |
scopus |
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