The kinetics of the gas-phase reaction of C1 atoms with CF31 have been studied relative to the reaction of C1 atoms with CH4 over the temperature range 271-363 K. Using k(C1 + CH4) = 9.6 X exp(-2680/RT) cm3 molecule-' s-', we derive k(C1 + CF3I) = 6.25 X lo-'' exp(-2970/RT) in which E , has units of
Conversion effect on the reaction CF3 + HCN. Analysis of I2 and I participation with CF3I as radical source
β Scribed by S. I. Lane; E. V. Oexler; E. H. Staricco
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 477 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
The gas-phase reaction of CF, with HCN has been examined over a wide conversion range using CF,I as a thermal and photolytic source of radicals. Quantitative and qualitative results show a significant increase of the specific rate constant for the hydrogen abstraction reaction relative to CF, recombination when reaction is carried out under ultraviolet irradiation. This "extra" formation of the reaction product, CF,H, has been assigned to the participation of iodine in this system through the formation of a (I-HCN) intermediate. Arrhenius parameters obtained for the addition mechanism of I to HCN do not seem to conform to a single reaction step, on the contrary, they correspond to a more complex reaction scheme.
π SIMILAR VOLUMES
By study of the NH&F2 and NH,-F-Fz-CF,I reaction systems, the emission spectra of NH\*, NH, N2 and NF species are obtained. The F atoms are generated by microwave discharge. The species produced in the reaction system appear in the order: NH\*, NH, Nz, NF. The vibrational and rotational temperatures
N-t-Butylacetamidines 1 on heating with methyl acrylate (2) at 200Λ gave the 4,5-dihydro-3H-pyridin-2one derivatives 5. Michael addition of the acetamidines 1 as their ene-1,1-diamine tautomers 1' to 2 and the subsequent cyclization of the adducts gave derivatives 5. Amidines 1 on reaction with trim
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