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Extreme ultraviolet time-resolved photoelectron spectroscopy of adenine, adenosine and adenosine monophosphate in a liquid flat jet.
Koga, Masafumi; Kang, Do Hyung; Heim, Zachary N; Meyer, Philipp; Erickson, Blake A; Haldar, Neal; Baradaran, Negar; Havenith, Martina; Neumark, Daniel M.
Afiliación
  • Koga M; Department of Chemistry, University of California, Berkeley, California 94720, USA. dneumark@berkeley.edu.
  • Kang DH; Department of Chemistry, University of California, Berkeley, California 94720, USA. dneumark@berkeley.edu.
  • Heim ZN; Department of Chemistry, University of California, Berkeley, California 94720, USA. dneumark@berkeley.edu.
  • Meyer P; Lehrstuhl für Physikalische Chemie II, Ruhr-Universität Bochum, 44801, Germany.
  • Erickson BA; Department of Chemistry, University of California, Berkeley, California 94720, USA. dneumark@berkeley.edu.
  • Haldar N; Department of Chemistry, University of California, Berkeley, California 94720, USA. dneumark@berkeley.edu.
  • Baradaran N; Department of Chemistry, University of California, Berkeley, California 94720, USA. dneumark@berkeley.edu.
  • Havenith M; Lehrstuhl für Physikalische Chemie II, Ruhr-Universität Bochum, 44801, Germany.
  • Neumark DM; Department of Chemistry, University of California, Berkeley, California 94720, USA. dneumark@berkeley.edu.
Phys Chem Chem Phys ; 26(17): 13106-13117, 2024 May 01.
Article en En | MEDLINE | ID: mdl-38629206
ABSTRACT
Time-resolved photoelectron spectroscopy using an extreme-ultraviolet (XUV) probe pulse was used to investigate the UV photoinduced dynamics of adenine (Ade), adenosine (Ado), and adenosine-5-monophosphate (AMP) in a liquid water jet. In contrast to previous studies using UV probe pulses, the XUV pulse at 21.7 eV can photoionize all excited states of a molecule, allowing for full relaxation pathways to be addressed after excitation at 4.66 eV. This work was carried out using a gas-dynamic flat liquid jet, resulting in considerably enhanced signal compared to a cylindrical jet. All three species decay on multiple time scales that are assigned based on their decay associated spectra; the fastest decay of ∼100 fs is assigned to ππ* decay to the ground state, while a smaller component with a lifetime of ∼500 fs is attributed to the nπ* state. An additional slower channel in Ade is assigned to the 7H Ade conformer, as seen previously. This work demonstrates the capability of XUV-TRPES to disentangle non-adiabatic dynamics in an aqueous solution in a state-specific manner and represents the first identification of the nπ* state in the relaxation dynamics of adenine and its derivatives.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Phys Chem Chem Phys Asunto de la revista: BIOFISICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Phys Chem Chem Phys Asunto de la revista: BIOFISICA / QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos