Mass-analyzed ion-kinetic-energy spectrometry

"MIKES" redirects here. For other uses, see Mikes.

Mass-analyzed ion-kinetic-energy spectrometry (MIKES) is a mass spectrometry technique by which mass spectra are obtained from a sector instrument that incorporates at least one magnetic sector plus one electric sector in reverse geometry (the beam first enters the magnetic sector).[1][2][3] The accelerating voltage V, and the magnetic field B, are set to select the precursor ions of a particular m/z. The precursor ions then dissociate or react in an electric field-free region between the two sectors. The ratio of the kinetic energy to charge of the product ions are analyzed by scanning the electric sector field E. The width of the product ion spectrum peaks is related to the kinetic energy release distribution for the dissociation process.[4]

See also

References

  1. ↑ Soltero-Rigau E, Kruger TL, Cooks RG (1977). "Identification of barbiturates by chemical ionization and mass-analyzed ion kinetic energy spectrometry". Anal. Chem. 49 (3): 435–42. doi:10.1021/ac50011a027. PMID 842853.
  2. ↑ Easton C, Johnson DW, Poulos A (1988). "Determination of phospholipid base structure by CA MIKES mass spectrometry". J. Lipid Res. 29 (1): 109–12. PMID 3356947.
  3. ↑ Cooks RG, Kondrat RW, Youssefi M, McLaughlin JL (1981). "Mass-analyzed ion kinetic energy (MIKE) spectrometry and the direct analysis of coca". J Ethnopharmacol 3 (2-3): 299–312. doi:10.1016/0378-8741(81)90060-X. PMID 7242113.
  4. ↑ Yeh, Chul; Myung Soo Kim (1992). "Analysis of a mass-analyzed ion kinetic energy profile. II. Systematic determination of the kinetic energy release distribution" (PDF). Rapid Communications in Mass Spectrometry 6 (4): 293–297. doi:10.1002/rcm.1290060414. Retrieved 2008-03-30.

Bibliography

  • Jacques Momigny; Eugen Illenberger (1999). Gaseous Molecular Ions: An Introduction To Elementary Processes Induced By Ionization (Topics in Physical Chemistry). Darmstadt: Steinkopff. ISBN 3-7985-0870-4. 
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