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Kinetic energy release in ionic fragmentations: Use as an ion structure probe
Author(s) -
Jones E. G.,
Bauman L. E.,
Bey J. H.,
Cooks R. G.
Publication year - 1973
Publication title -
organic mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.475
H-Index - 121
eISSN - 1096-9888
pISSN - 0030-493X
DOI - 10.1002/oms.1210070208
Subject(s) - kinetic energy , metastability , ion , fragmentation (computing) , ionic bonding , atomic physics , electron ionization , chemistry , dissociation (chemistry) , physics , ionization , organic chemistry , quantum mechanics , computer science , operating system
The kinetic energy released in unimolecular reactions, as measured from the width of the corresponding metastable peak, shows only a small dependence on such parameters as source temperature, ion‐source residence time and ion acceleration voltage. Similarly, fragmenting ions generated from different members of an homologous series of molecular ions have been found to release the same kinetic energy and hence do not exhibit a degrees‐of‐freedom effect analogous to that for metastable abundances. In general, molecular ions formed by electron‐impact have been found to release slightly less kinetic energy on fragmentation than the corresponding ions formed via a fragmentation sequence. These observations suggest that kinetic energy release is a useful method of structural characterization of metastable ions; while increase in the average internal energies of the ions sample lead to larger energy releases, this effect is usually small. The use of a very narrow energy resolving (β) slit and a procedure in which the metastable peak width is extrapolated to zero slit width has been found to improve the accuracy of measurement of the kinetic energy release, particularly when the metastable and main beam peak widths are of comparable magnitude.