Fourier transform infrared study of the gas-phase reaction of ozone-18O3 with trans-1,2-dichloroethene in oxygen-16O2-rich mixtures. Branching ratio for oxygen atom production via dissociation of the primary Criegee intermediate

1984 ◽  
Vol 88 (4) ◽  
pp. 766-769 ◽  
Author(s):  
H. Niki ◽  
P. D. Maker ◽  
C. M. Savage ◽  
L. P. Breitenbach ◽  
R. I. Martinez

1982 ◽  
Vol 86 (10) ◽  
pp. 1858-1861 ◽  
Author(s):  
H. Niki ◽  
P. D. Maker ◽  
C. M. Savage ◽  
L. P. Breitenbach ◽  
R. I. Martinez ◽  
...  


1979 ◽  
Vol 57 (10) ◽  
pp. 1238-1243 ◽  
Author(s):  
Walter A. Aue ◽  
Zbigniew M. Mielniczuk

Gas chromatographic effluents were detected by their quenching effect on the luminescence of a steady 'cold flame', as provided by the gas-phase reaction of phosphorus vapor and oxygen. The response of organic compounds correlated with their 'ease of oxidation' in accordance with the literature, suggesting that such compounds act as oxygen atom scavengers in the branched-chain P4/O2 reaction.Most substances showed linear response over one to two orders of magnitude, and minimum detectable amounts ranged from 2 × 10−9g (benzaldehyde) to 2 × 10−4g (dichloromethane). The detector temperature could be varied to (a) alter response ratios, i.e. selectivity, among some types of compounds; and (b) produce easily-obtained Arrhenius plots. However, the response (luminescence quenching) of most compounds was independent of temperature over a considerable range.



1989 ◽  
Vol 3 (9) ◽  
pp. 298-299 ◽  
Author(s):  
M. Decouzon ◽  
J-F. Gal ◽  
S. Géribaldi ◽  
M. Rouillard ◽  
J-M. Sturla ◽  
...  


ChemInform ◽  
2010 ◽  
Vol 23 (37) ◽  
pp. no-no
Author(s):  
T. J. WALLINGTON ◽  
J. M. ANDINO ◽  
A. R. POTTS ◽  
O. J. NIELSEN


1992 ◽  
Vol 24 (7) ◽  
pp. 649-663 ◽  
Author(s):  
Timothy J. Wallington ◽  
Jean M. Andino ◽  
Alan R. Potts ◽  
Ole J. Nielsen


1981 ◽  
Vol 59 (9) ◽  
pp. 1357-1360 ◽  
Author(s):  
D. G. Cameron ◽  
S. C. Hsi ◽  
J. Umemura ◽  
H. H. Mantsch

Using a Fourier transform spectrometer the frequencies and bandwidths of the infrared active C—H stretching modes of n-octane were determined in a variety of solvents with refractive indices from 1.63 (carbon disulfide) to 1.28 (n-perfluorooctane), and dielectric constants from 37.5 (acetonitrile) to 1.8 (n-perfluorooctane). The frequency shifts were correlated with the refractive indices and dielectric constants of the solvents, and fitted with the equation of David and Hallam (Spectrochim. Acta, Part A, 23, 593 (1967)). Generally, solution results in shifts to frequencies lower than those observed in the gas phase. However, solution in n-perfluorooctane resulted in a shift to a higher frequency, behavior in accord with the above equation but not previously observed.



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