Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/1842
Title: Determination of bond dissociation energies using mass spectrometry
Authors: Nakat, Hanna El 
Ghanem, Noha
Yammine, Paolo 
Willett, Garry
Fisher, Keith
Affiliations: Department of Chemistry 
Department of Chemistry 
Issue Date: 2007
Part of: International journal of Quantum chemistry
Volume: 107
Issue: 6
Start page: 1367
End page: 1372
Abstract: 
Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR/MS) offers the opportunity for gas phase cluster formation reactions at very low pressures and at temperatures that are different from room temperature. Reactions take place with single positive-charge metal ions that are normally +2, +3, +4, etc., charged in solution. The ions formed are detected by measuring the current induced by their cyclotron rotation, but they cannot be physically separated and collected. Collision-induced dissociation (CID) is widely used for ion-structure determination via the fragmentation of the excited ions. CID study aims to determine the relationship between the Vpp [peak-to-peak voltage of the radiofrequency (rf) pulse] and the mass-to-charge (m/z) ratio, which will be used for the calculation of the center-of-mass translational kinetic energy (Ekcm) of the excited ion under investigation. CID studies are restricted to stable ions with relatively high abundance. Nevertheless, with the evolution of computational chemistry, such problems can be overcome whereby CID calculations will be used to provide the substantial parameters for computer software, such as the Gaussian 03 program, for the structure determination of the less stable NixSmath image anions. The latter constitutes the core for our current research. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007.
URI: https://scholarhub.balamand.edu.lb/handle/uob/1842
Ezproxy URL: Link to full text
Type: Journal Article
Appears in Collections:Department of Chemistry

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