We study gas-phase photodissociation of radiosensitizer molecules nimorazole and metronidazole with the focus on the yield of the oxygen mimics nitrogen oxides and nitrous acid. Regardless of photon energy, we find the nimorazole cation to split the intramolecular bridge with little NO or NO production, which makes the molecule a precursor of dehydrogenated methylnitroimidazole. Metronidazole cation, on the contrary, has numerous fragmentation pathways with strong energy dependence. Most notably, ejection of NOOH and NO takes place within 4 eV from the valence ionization energy. Whereas the NO ejection is followed by further fragmentation steps when energy so allows, we find emission of NOOH takes place in microsecond time-scales and as a slow process that is relevant only when no other competing reaction is feasible. These primary dissociation characteristics of the molecules are understood by applying the long-known principle of rapid internal conversion of the initial electronic excitation energy and by studying the energy minima and the saddle points on the potential energy surface of the electronic ground state of the molecular cation.
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http://dx.doi.org/10.1021/acs.jpca.0c03045 | DOI Listing |
ACS Cent Sci
December 2024
Department of Chemistry and Biochemistry, University of California at Los Angeles, Los Angeles, California 90095, United States.
Electron microscopy in its various forms is one of the most powerful imaging and structural elucidation methods in nanotechnology where sample information is generally limited by random chemical and structural damage. Here we show how a well-selected chemical probe can be used to transform indiscriminate chemical damage into clean chemical processes that can be used to characterize some aspects of the interactions between high-energy electron beams and soft organic matter. Crystals of a Dewar benzene exposed to a 300 keV electron beam facilitate a clean valence-bond isomerization radical-cation chain reaction where the number of chemical events per incident electron is amplified by a factor of up to ca.
View Article and Find Full Text PDFNature
December 2024
Institute of Physics, University of Freiburg, Freiburg, Germany.
Tailored light-matter interactions in the strong coupling regime enable the manipulation and control of quantum systems with up to unit efficiency, with applications ranging from quantum information to photochemistry. Although strong light-matter interactions are readily induced at the valence electron level using long-wavelength radiation, comparable phenomena have been only recently observed with short wavelengths, accessing highly excited multi-electron and inner-shell electron states. However, the quantum control of strong-field processes at short wavelengths has not been possible, so far, because of the lack of pulse-shaping technologies in the extreme ultraviolet (XUV) and X-ray domain.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Technische Universität Braunschweig, Institut für Physikalische und Theoretische Chemie, Gaussstraße 17, D-38106 Braunschweig, Germany.
In this work, the development of a new general-purpose exchange-correlation hybrid functional based on the recent locally range-separated local hybrid approach is presented. In particular, the new functional, denoted as MH24, combines a non-empirical treatment of the admixture of locally range-separated long-range exact exchange with a new real-space separation approach for the real-space exact-exchange admixture governed by the local mixing function (LMF) and a new empirical LYP-based approach for the correlation functional to enable a flexible description of same- and opposite-spin correlation effects. The nine empirical parameters of the MH24 model have been optimized using a state-of-the-art super-self-consistent-field approach, which exploits the sensitivity of specific properties, such as core ionization potentials, electron affinities, and atomization energies, to the exact-exchange admixture in specific regions in real space and the separation of the LMF into a core, valence, and asymptotic part.
View Article and Find Full Text PDFSoft Matter
December 2024
Institute of Physical Chemistry, RWTH Aachen University, Landoltweg 2, 52056 Aachen, Germany.
Phys Chem Chem Phys
December 2024
Department of Chemistry and Institute for Molecular Science and Fusion Technology, Kangwon National University, Chuncheon 24341, Republic of Korea.
Pyridine derivatives are fundamental in fields such as organic chemistry, materials science, and pharmaceuticals, largely due to their versatile electronic properties. Fluorination of pyridine significantly alters these properties, yet the specific effects of the position and number of fluorine atoms on valence orbitals and cationic structures remain not fully understood. This study examines the impact of fluorine substitution on the valence orbitals and cationic structures of various pyridine derivatives, with a particular emphasis on 2,6-difluoropyridine (2,6-DFP).
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