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Determination of bond dissociation energies using mass spectrometry
Author(s) -
ElNakat John Hanna,
Ghanem Noha,
Yammine Paolo,
Willett Gary,
Fisher Keith
Publication year - 2006
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.21261
Subject(s) - fourier transform ion cyclotron resonance , chemistry , mass spectrometry , ion , dissociation (chemistry) , fragmentation (computing) , excited state , collision induced dissociation , ion cyclotron resonance , kinetic energy , analytical chemistry (journal) , atomic physics , tandem mass spectrometry , cyclotron , physics , organic chemistry , chromatography , quantum mechanics , computer science , operating system
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 V pp [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 (Ek cm ) 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 Ni x S y −anions. The latter constitutes the core for our current research. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2007