Please use this identifier to cite or link to this item: http://repository.aaup.edu/jspui/handle/123456789/13
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dc.contributor.authorfaady m. siouri-
dc.contributor.authorsamuel boldissar, $Other$Other-
dc.contributor.authorjacob berenbeim, $Other$Other-
dc.contributor.authormattanjah de vries, $Other$Other-
dc.date.accessioned2019-11-06T06:36:49Z-
dc.date.available2019-11-06T06:36:49Z-
dc.date.issued2017-06-26-
dc.identifier.urihttp://repository.aaup.edu/jspui/handle/123456789/13-
dc.description.abstractHere we present the excited state dynamics of jet-cooled 6-thioguanine (6-TG), using resonance-enhanced multiphoton ionization (REMPI), IR–UV double resonance spectroscopy, and pump–probe spectroscopy in the nanosecond and picosecond time domains. We report data on two thiol tautomers, which appear to have different excited state dynamics. These decay to a dark state, possibly a triplet state, with rates depending on tautomer form and on excitation wavelength, with the fastest rate on the order of 1010 s–1. We also compare 6-TG with 9-enolguanine, for which we observed decay to a dark state with a 2 orders of magnitude smaller rate. At increased excitation energy (?+500 cm–1) an additional pathway appears for the predominant thiol tautomer. Moreover, the excited state dynamics for 6-TG thiols is different from that recently predicted for thiones.en_US
dc.language.isoen_USen_US
dc.publisherThe Journal of Physical Chemistry Aen_US
dc.titleExcited State Dynamics of 6-Thioguanineen_US
dc.typeArticleen_US
Appears in Collections:Faculty & Staff Scientific Research publications

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