Direct Time-Resolved Study of the Gas-Phase Reactions of Germylene with Ethyl- and Diethylgermane:  Absolute Rate Constants, Temperature Dependences, and Mechanism

2007 ◽  
Vol 111 (8) ◽  
pp. 1434-1440 ◽  
Author(s):  
Rosa Becerra ◽  
Sergey E. Boganov ◽  
Mikhail P. Egorov ◽  
Irina V. Krylova ◽  
Oleg M. Nefedov ◽  
...  
1983 ◽  
Vol 61 (12) ◽  
pp. 2716-2720 ◽  
Author(s):  
John M. Roscoe

The reactions of O(3P) with the butanols were studied kinetically as a function of temperature and substrate concentration. The absolute rate constants for the gas phase reactions, in the units M−1 s−1, obey the following relations.[Formula: see text]The results suggest that although the α-CH bond in these alcohols is the most reactive one, reaction of O(3P) with other CH bonds in the alcohols is also appreciable. The kinetic data for these and other alcohols are separated into contributions from the different types of CH bonds and the results are discussed in terms of linear free energy relations.


2006 ◽  
Vol 417 (4-6) ◽  
pp. 480-485 ◽  
Author(s):  
Pablo M. Cometto ◽  
Mariano A. Teruel ◽  
Raúl A. Taccone ◽  
Silvia I. Lane

1972 ◽  
Vol 50 (14) ◽  
pp. 2230-2235 ◽  
Author(s):  
J. D. Payzant ◽  
A. J. Cunningham ◽  
P. Kebarle

The rate constants for the forward and reverse components of gas phase reactions:[Formula: see text]were measured with a pulsed electron beam, time resolved detection high pressure mass spectrometer at 300 °K. O2, Ar, and He at pressures from 1–7 Torr were used as third gas M. The forward reactions were found to be third order and the reverse reactions second order. Establishment of the equilibria could also be observed.


1990 ◽  
Vol 86 (1) ◽  
pp. 27 ◽  
Author(s):  
James E. Baggott ◽  
H. Monty Frey ◽  
Phillip D. Lightfoot ◽  
Robin Walsh ◽  
Ivy M. Watts

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