Threshold photoelectron spectroscopy of 9-methyladenine: theory and experiment.

Phys Chem Chem Phys

Université Gustave Eiffel, COSYS/LISIS, 5 Bd Descartes 77454, Champs-sur-Marne, France.

Published: February 2022

We present a combined experimental and theoretical study of single-photon ionization of 9-methyladenine (9MA) in the gas phase. In addition to tautomerism, several rotamers due to the rotation of the methyl group may exist. Computations show, however, that solely one rotamer contributes because of low population in the molecular beam and/or unfavorable Franck-Condon factors upon ionization. Experimentally, we used VUV radiation available at the DESIRS beamline of the synchrotron radiation facility SOLEIL to record the threshold photoelectron spectrum of this molecule between 8 and 11 eV. This spectrum consists of a well-resolved band assigned mainly to vibronic levels of the D cationic state, plus a contribution from the D state, and two large bands corresponding to the D, D and D electronically excited states. The adiabatic ionization energy of 9MA is measured at 8.097 ± 0.005 eV in close agreement with the computed value using the explicitly correlated coupled cluster approach including core valence, scalar relativistic and zero-point vibrational energy corrections. This work sheds light on the complex pattern of the lowest doublet electronic states of 9MA. The comparison to canonical adenine reveals that methylation induces further electronic structure complication that may be important to understand the effects of ionizing radiation and the charge distribution in these biological entities at different time scales.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d1cp03729cDOI Listing

Publication Analysis

Top Keywords

threshold photoelectron
8
photoelectron spectroscopy
4
spectroscopy 9-methyladenine
4
9-methyladenine theory
4
theory experiment
4
experiment combined
4
combined experimental
4
experimental theoretical
4
theoretical study
4
study single-photon
4

Similar Publications

In molecular beam scattering experiments, an important technique for measuring product energy and angular distributions is velocity map imaging following photoionization of one or more scattered species. For studies with cold molecular beams, the ultimate resolution of such a study is often limited by the product detection process. When state-selective ionization detection is used, excess energy from the ionization step can transfer to kinetic energy in the target molecular ion-electron pair, resulting in measurable cation recoil.

View Article and Find Full Text PDF

The application of perovskite oxide for high-temperature electrocatalysis is hindered by its limited activity. Exsolution is a smart strategy that allows the enrichment of the perovskite's surface with highly reactive phases, yielding heteroboundaries. However, the identification of the exact catalytic role of this complex architecture is still elusive.

View Article and Find Full Text PDF

Observation of Attosecond Time Delays in Above-Threshold Ionization.

Phys Rev Lett

November 2024

Wuhan National Laboratory for Optoelectronics and School of Physics, Huazhong University of Science and Technology, Wuhan 430074, China.

Attosecond-scale temporal characterization of photoionization is essential in understanding how light and matter interact on the most fundamental level. However, characterizing the temporal property of strong-field above-threshold ionization has remained unreached. Here, we propose a novel photoelectron interferometric method to disentangle the contribution of Coulomb effect from an attoclock, allowing us to clock energy-resolved time delays of strong-field above-threshold ionization.

View Article and Find Full Text PDF

We report vibrationally resolved threshold photoelectron spectra of several sulfur-containing reactive intermediates. This includes the organosulfur radicals CHS, CHS, CHSH, CHS, and SH, which are relevant in atmospheric chemistry and in astrochemical settings. Due to the high reactivity, the radicals were prepared pyrolysis of (CH)S.

View Article and Find Full Text PDF

Graphene oxide (GO) possesses specific properties that are revolutionizing materials science, with applications extending from flexible electronics to advanced nanotechnology. A key method for harnessing GO's potential is its laser-induced reduction, yet the exact mechanisms - photothermal versus photochemical effects - remain unclear. Herein, we discover the dominant role of photochemical reactions in the laser reduction of GO under visible light, challenging the prevailing assumption that photothermal effects are dominant.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!