Please use this identifier to cite or link to this item:
http://repository.aaup.edu/jspui/handle/123456789/13
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | faady m. siouri | - |
dc.contributor.author | samuel boldissar, $Other$Other | - |
dc.contributor.author | jacob berenbeim, $Other$Other | - |
dc.contributor.author | mattanjah de vries, $Other$Other | - |
dc.date.accessioned | 2019-11-06T06:36:49Z | - |
dc.date.available | 2019-11-06T06:36:49Z | - |
dc.date.issued | 2017-06-26 | - |
dc.identifier.uri | http://repository.aaup.edu/jspui/handle/123456789/13 | - |
dc.description.abstract | Here 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.iso | en_US | en_US |
dc.publisher | The Journal of Physical Chemistry A | en_US |
dc.title | Excited State Dynamics of 6-Thioguanine | en_US |
dc.type | Article | en_US |
Appears in Collections: | Faculty & Staff Scientific Research publications |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
Excited State Dynamics of 6-Thioguanine.pdf | 2.64 MB | Adobe PDF | ![]() View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
Admin Tools