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Open AccessArticle

The Role of Electron Transfer in the Fragmentation of Phenyl and Cyclohexyl Boronic Acids

1
Atomic and Molecular Collisions Laboratory, CEFITEC, Department of Physics, Universidade NOVA de Lisboa, 2829-516 Caparica, Portugal
2
Department of Theoretical Physics and Quantum Information, Gdańsk University of Technology, Narutowicza 11/12, 80-233 Gdańsk, Poland
3
Instituto de Física Fundamental, Consejo Superior de Investigaciones Científicas (CSIC), Serrano 113-bis, 28006 Madrid, Spain
4
Institute for Medicines and Pharmaceutical Sciences (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisbon, Portugal
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2019, 20(22), 5578; https://doi.org/10.3390/ijms20225578
Received: 23 October 2019 / Revised: 5 November 2019 / Accepted: 6 November 2019 / Published: 8 November 2019
(This article belongs to the Special Issue Radiation-Induced Damage to DNA)
In this study, novel measurements of negative ion formation in neutral potassium-neutral boronic acid collisions are reported in electron transfer experiments. The fragmentation pattern of phenylboronic acid is comprehensively investigated for a wide range of collision energies, i.e., from 10 to 1000 eV in the laboratory frame, allowing some of the most relevant dissociation channels to be probed. These studies were performed in a crossed molecular beam set up using a potassium atom as an electron donor. The negative ions formed in the collision region were mass analysed with a reflectron time-of-flight mass spectrometer. In the unimolecular decomposition of the temporary negative ion, the two most relevant yields were assigned to BO and BO2. Moreover, the collision-induced reaction was shown to be selective, i.e., at energies below 100 eV, it mostly formed BO, while at energies above 100 eV, it mostly formed BO2. In order to further our knowledge on the complex internal reaction mechanisms underlying the influence of the hybridization state of the boron atom, cyclohexylboronic acid was also investigated in the same collision energy range, where the main dissociation channel yielded BO2. The experimental results for phenyl boronic acid are supported by ab initio theoretical calculations of the lowest unoccupied molecular orbitals (LUMOs) accessed in the collision process. View Full-Text
Keywords: boronic acids; electron transfer; TOF mass spectrometry; negative ion formation boronic acids; electron transfer; TOF mass spectrometry; negative ion formation
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MDPI and ACS Style

Lozano, A.I.; Pamplona, B.; Kilich, T.; Łabuda, M.; Mendes, M.; Pereira-da-Silva, J.; García, G.; Gois, P.M.P.; Ferreira da Silva, F.; Limão-Vieira, P. The Role of Electron Transfer in the Fragmentation of Phenyl and Cyclohexyl Boronic Acids. Int. J. Mol. Sci. 2019, 20, 5578.

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