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.
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http://dx.doi.org/10.1039/d1cp03729c | DOI Listing |
J Phys Chem A
December 2024
Radboud University Nijmegen, Institute for Molecules and Materials, Heijendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.
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 PDFJ Am Chem Soc
January 2025
College of Energy, Xiamen University, Xiamen 361005, China.
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 PDFPhys 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 PDFPhys Chem Chem Phys
November 2024
University of Würzburg, Institute of Physical and Theoretical Chemistry, Am Hubland, 97074 Würzburg, Germany.
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 PDFNat Commun
November 2024
Tomsk Polytechnic University, Lenina ave. 30, Tomsk, 634050, Russia.
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.
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