Reaction of Active Nitrogen with Tetrachloroethylene

1973 ◽  
Vol 51 (22) ◽  
pp. 3680-3683 ◽  
Author(s):  
William Ernest Jones ◽  
Manit Rujimethabhas

The reaction of active nitrogen with tetrachloroethylene yielded cyanogen chloride, trichloroacetonitrile, cyanogen, chlorine, and carbon tetrachloride. In addition, a yellow–brown polymer was found on the glass wall. A brief discussion of a possible mechanism is given.


1958 ◽  
Vol 36 (9) ◽  
pp. 1223-1226 ◽  
Author(s):  
S. E. Sobering ◽  
C. A. Winkler

Cyanogen chloride and chlorine were the only gaseous products observed in the reaction of active nitrogen with carbon tetrachloride at 110° and 420 °C. The product yields tended towards limiting values at higher reactant flow rates, and increased with increase of temperature at all flow rates. The reactions of active nitrogen with chloroform and dichloromethane at 260° and 420 °C yielded hydrogen chloride, hydrogen cyanide, and cyanogen, in addition to cyanogen chloride and chlorine. The behavior of the product yields with reactant flow rates and temperature was similar to that of the products from carbon tetrachloride.



1958 ◽  
Vol 36 (1) ◽  
pp. 127-133 ◽  
Author(s):  
R. N. Dixon ◽  
R. W. Nicholls

Experimental band intensities in the CN red system, A (2Πi) →X(2Σ+), have been measured using an active nitrogen – carbon tetrachloride source. Using calculated Franck–Condon factors qν′ν″ the electronic transition moment Re(r) is found to vary little over the range 1.04 < r < 1.27 Å.



1982 ◽  
Vol 18 (4) ◽  
pp. 301-305 ◽  
Author(s):  
V. Sáez Rábanos ◽  
F. Tabarés ◽  
A. González Ureña


This paper deals in the first place with the effect of minute gaseous impurities which have apparently an important effect in promoting the formation of active nitrogen by the electric discharge. Oxygen is one of them. It is shown that the action of oxygen must be on the walls of the tube: for when a minute oxygen tributary is added to the nitrogen stream, it takes much longer to assert its action than the time required to establish the changed composition of the gas stream: and similarly when the oxygen tributary is checked its activity persists for a time. This is interpreted to mean that the action of the oxygen or other impurity is to modify the glass wall in a way favourable to the accumulation of active nitrogen. The restoration of the afterglow by addition of tributary stream of oxygen can be observed even better with the electrodeless discharge at low pressure (0.3 mm. say) than with high-pressure electrical discharges at say 3 mm. pressure. The intensity in some experiments has been raised 32-fold by the admission of oxygen. Under certain conditions of the glass the cutting off of the oxygen tributary causes a temporary fall of intensity to considerably less than the static value, followed by a rise to that static value. This shows that the phenomena are complicated and not likely to admit of any very simple analysis. The paper goes on to examine how various treatments of a glass vessel affect its action on the afterglow. As found by Herzberg strong preliminary heating in vacuo makes it destructive of the glow. It is now shown that heating in nitrogen at atmospheric pressure does the same. Heating in oxygen, even at 1 mm. pressure, restores it. It seems clear that these effects cannot easily be explained by the formation or removal of gas layers. The behaviour of glass is therefore very complex, and not likely to be easily unravelled. The behaviour of the gas itself away from any surface is more fundamental. By a special device it is shown that in this case the purest nitrogen is the best, and that the addition of a trace of oxygen has no favourable effect in promoting the active nitrogen phenomena.



Photoelectric intensity measurements in emission have been made at medium and high resolution on the CN violet system which was excited in the active nitrogen-carbon tetrachloride afterglow. Line and band intensity profiles have been interpreted in terms of transition probability parameters through comparison with realistic computer-synthesized spectra.



Emission of the CN red (A -> X) and violet (B -> X) systems accompanying the reactions of active nitrogen with cyanogen, hydrogen cyanide, cyanogen chloride and methylene chloride and of oxygen atoms with cyanogen have been investigated. Bayes’s classification of the rod emission into the vibrational distributions P 1 (v' ≤ 3) and P 2 (v' ≥ 3) can be extended to the violet system, emission from levels 15 ≥ v' ≥ 5 accompanying the P 1 distribution and emission from level v' = 0 occurring with the P 2 emission. It is shown that the P 1 distribution and the excitation of the high vibrational levels of the violet system are due to collisions of CN with energetic species or CN acting as a third body for atomic recombination. The P 2 distribution is associated with the formation of electronically excited CN in exothermic transfer reactions such as N + CH = NC + H, N + CCl = NC + Cl



2001 ◽  
Vol 120 (5) ◽  
pp. A715-A715
Author(s):  
Y NAKADE ◽  
M YONEDA ◽  
S TAKAMOTO ◽  
T ITO ◽  
S OKAMOTO ◽  
...  


2000 ◽  
Vol 87 (5) ◽  
pp. 229-233 ◽  
Author(s):  
Beatrice Arosio ◽  
Nicoletta Gagliano ◽  
Lorena Maria Pia Fusaro ◽  
Luciano Parmeggiani ◽  
Jacopo Tagliabue ◽  
...  


Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
YJ Moon ◽  
WC Lee ◽  
SJ Kim ◽  
ST Oh ◽  
EJ Shin ◽  
...  


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