4.6 Article

Excited State Dynamics of 6-Thioguanine

Journal

JOURNAL OF PHYSICAL CHEMISTRY A
Volume 121, Issue 28, Pages 5257-5266

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpca.7b03036

Keywords

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Funding

  1. National Aeronautics and Space Administration [NNX12AG77G]
  2. National Science Foundation [CHE-1301305]
  3. CNSI
  4. MRL: an NSF MRSEC [DMR-1121053]
  5. NSF [CNS-0960316]
  6. Center for Scientific Computing
  7. Division Of Chemistry
  8. Direct For Mathematical & Physical Scien [1301305] Funding Source: National Science Foundation

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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 10(10) 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 (similar to+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.

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