scholarly journals Zur Photoionisation und Ionenfragmentation von SF4/Photoionization and Ion Fragmentation of SF4

1989 ◽  
Vol 44 (1) ◽  
pp. 13-16 ◽  
Author(s):  
H.-W. Jochims ◽  
E. Rühl ◽  
H. Baumgärtel
Keyword(s):  
Mass Spectrometry ◽  
Photoelectron Spectroscopy ◽  
Theoretical Calculations ◽  
Ionization Potentials ◽  
Bond Dissociation Energies ◽  
Bond Dissociation ◽  
Photoionization Mass Spectrometry ◽  
Ion Fragmentation ◽  
Dissociation Energies

Abstract The ionization potentials of sulfurtetrafluoride have been measured using threshold photoelectron spectroscopy and com pared with theoretical calculations. The decay of SF4+ has been studied by photoionization mass spectrometry and photoion-photoelectron coincidence. The break-down graphs reveal competing decay processes. Bond dissociation energies in SF4+ have been calculated.

FREE RADICALS BY MASS SPECTROMETRY: X. THE IONIZATION POTENTIALS OF METHYL SUBSTITUTED ALLYL RADICALS

1956 ◽  
Vol 34 (3) ◽  
pp. 345-353 ◽  
Author(s):  
C. A. McDowell ◽  
F. P. Lossing ◽  
I. H. S. Henderson ◽  
J. B. Farmer
Keyword(s):  
Mass Spectrometry ◽  
Free Radicals ◽  
Electron Impact ◽  
Heat Of Formation ◽  
Ionization Potentials ◽  
Bond Dissociation Energies ◽  
Allyl Radical ◽  
Dissociation Energies ◽  
Allyl Halides ◽  
Vertical Ionization Potentials

The vertical ionization potentials of the β- and γ-methyl substituted allyl radicals as measured by electron impact are 8.03 ± 0.05 v. and 7.71 ± 0.05 v, respectively. From appearance potential data the following bond dissociation energies can be derived, assuming the dissociation processes to be free from complications:[Formula: see text]With assumptions about the structure of the ions produced by electron impact from the corresponding butenes the dissociation energies of the C4H7—H bonds in these latter compounds can be estimated, and the heats of formation of the corresponding radicals derived, namely:[Formula: see text]From data on the allyl halides we evaluate the heat of formation of the allyl radical to be:[Formula: see text]

FREE RADICALS BY MASS SPECTROMETRY: VII. THE IONIZATION POTENTIALS OF ETHYL, ISOPROPYL, AND PROPARGYL RADICALS AND THE APPEARANCE POTENTIALS OF THE RADICAL IONS IN SOME DERIVATIVES

1955 ◽  
Vol 33 (5) ◽  
pp. 861-869 ◽  
Author(s):  
J. B. Farmer ◽  
F. P. Lossing
Keyword(s):  
Mass Spectrometry ◽  
Thermal Decomposition ◽  
Free Radicals ◽  
Kinetic Energy ◽  
Electron Impact ◽  
Ionization Potentials ◽  
Bond Dissociation Energies ◽  
Radical Ions ◽  
Dissociation Energies ◽  
Propargyl Radicals

The ionization potentials of ethyl, isopropyl, and propargyl radicals have been measured by electron impact on radicals produced by thermal decomposition of appropriate compounds. The values are:ethyl 8.78±0.05 ev., isopropyl 7.90±0.05 ev., and propargyl 8.25±0.08 ev. From the appearance potentials of these ions in various compounds, the following values of bond dissociation energies were obtained:[Formula: see text][Formula: see text] assuming no kinetic energy of the products.

Determination of Ruthenium−Phosphorus Bond Dissociation Energies by ES-FTICR Mass Spectrometry

2002 ◽  
Vol 21 (26) ◽  
pp. 5688-5691 ◽  
Author(s):  
John B. Westmore ◽  
Lisa Rosenberg ◽  
Timothy S. Hooper ◽  
Gary D. Willett ◽  
Keith J. Fisher
Keyword(s):  
Mass Spectrometry ◽  
Bond Dissociation Energies ◽  
Fticr Mass Spectrometry ◽  
Bond Dissociation ◽  
Dissociation Energies

Determination of bond dissociation energies using mass spectrometry

2007 ◽  
Vol 107 (6) ◽  
pp. 1367-1372 ◽  
Author(s):  
John Hanna El-Nakat ◽  
Noha Ghanem ◽  
Paolo Yammine ◽  
Gary Willett ◽  
Keith Fisher
Keyword(s):  
Mass Spectrometry ◽  
Bond Dissociation Energies ◽  
Bond Dissociation ◽  
Dissociation Energies
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