- Mass Spectrometry Techniques and Applications
- Spectroscopy and Quantum Chemical Studies
- Advanced Chemical Physics Studies
- Coordination Chemistry and Organometallics
- Analytical Chemistry and Chromatography
- Photoreceptor and optogenetics research
- Catalytic Processes in Materials Science
- Cold Atom Physics and Bose-Einstein Condensates
- Radioactive element chemistry and processing
- Nanomaterials for catalytic reactions
- Ammonia Synthesis and Nitrogen Reduction
- Chemical Reactions and Isotopes
- Atomic and Molecular Physics
Hebrew University of Jerusalem
2023-2025
Ariel University
2020
Mutual neutralization of hydronium (H
<title>Abstract</title> The mutual-neutralization of hydronium and hydroxide ions is a fundamental chemical reaction. Yet, there very limited direct experimental evidence about its intrinsically non-adiabatic mechanism. By 3D-imaging the coincident neutral products isolated D<sub>3</sub>O<sup>+</sup> OD<sup>−</sup> reactions, we revealed two competing pathways leading to distinct D<sub>2</sub>O+OD+D 2OD+D<sub>2</sub> product channels substantial suppression proton-transfer mechanism due...
Simultaneous trapping of merged cation and anion beams in the HEIBT paves way for controlled MN molecular cluster ions.
The mechanism of reduction AuCl4–/AuCl3OH– by BH4– was analyzed density functional theory (DFT). results point out that Auatoms0 are not intermediates in the process. derived differs considerably from reported for analogous process involving Ag(H2O)2+ BH4–. Thus, though both processes follow Creighton procedure, detailed significantly. For Au, agglomeration starts with AuH2–, whereas Ag, it (H2O)AgH. Stopped-flow measurements support complicated mechanism.