scholarly journals Gas Phase Reactions of 1,3,5-Triazine: Proton Transfer, Hydride Transfer, and Anionic σ-Adduct Formation

2011 ◽  
Vol 22 (7) ◽  
pp. 1260-1272 ◽  
Author(s):  
John M. Garver ◽  
Zhibo Yang ◽  
Shuji Kato ◽  
Scott W. Wren ◽  
Kristen M. Vogelhuber ◽  
...  
1981 ◽  
Vol 59 (11) ◽  
pp. 1615-1621 ◽  
Author(s):  
Scott D. Tanner ◽  
Gervase I. Mackay ◽  
Diethard K. Bohme

Flowing afterglow measurements are reported which provide rate constants and product identifications at 298 ± 2 K for the gas-phase reactions of OH− with CH3OH, C2H5OH, CH3OCH3, CH2O, CH3CHO, CH3COCH3, CH2CO, HCOOH, HCOOCH3, CH2=C=CH2, CH3—C≡CH, and C6H5CH3. The main channels observed were proton transfer and solvation of the OH−. Hydration with one molecule of H2O was observed either to reduce the rate slightly and lead to products which are the hydrated analogues of the "nude" reaction, or to stop the reaction completely, k ≤ 10−12 cm3 molecule−1 s−1. The reaction of OH−•H2O with CH3—C≡CH showed an uncertain intermediate behaviour.


1990 ◽  
Vol 112 (7) ◽  
pp. 2537-2541 ◽  
Author(s):  
Russell J. Waugh ◽  
Roger N. Hayes ◽  
Peter C. H. Eichinger ◽  
K. M. Downard ◽  
John H. Bowie

1995 ◽  
Vol 395 ◽  
Author(s):  
A. Thon ◽  
T.F. Kuech

ABSTRACTGas phase reactions between trimethylgallium (TMG) and ammonia were studied at high temperatures, characteristic to MOCVD of GaN reactors, by means of insitu mass spectroscopy in a flow tube reactor. It is shown, that a very fast adduct formation followed by elimination of methane occurs. The decomposition of TMG and the adduct - derived compounds are both first order and have similar apparent activation energy. The pre-exponential factor of the adduct decomposition is smaller, and hence is responsible for the higher full decomposition temperature of the adduct relative to that of TMG.


1984 ◽  
Vol 62 (8) ◽  
pp. 1465-1469 ◽  
Author(s):  
Saul Wolfe

At the 3-21G (3-21G*) computational level, the intrinsic barriers associated with proton transfer between XCH2− and CH3X have been found to be essentially constant (ca. 10 kcal/mol) for X = H, F, SH, Cl. According to the Marcus rate-equilibrium treatment of proton transfer reactions, this result means that transition states should not exist for gas phase reactions [Formula: see text], when the energy change exceeds 20 kcal/mol. This prediction has been confirmed for two cases (X = H, F) in which the energy change is less than 20 kcal/mol, and two cases (X = SH, Cl) in which the energy change is greater than 20 kcal/mol.


2008 ◽  
Vol 336 (1-2) ◽  
pp. 116-127 ◽  
Author(s):  
Mario Benassi ◽  
Patricia V. Abdelnur ◽  
Marcos N. Eberlin ◽  
Takao Okazaki ◽  
Kenneth K. Laali

1974 ◽  
Vol 5 (42) ◽  
pp. no-no
Author(s):  
I. DZIDIC ◽  
D. I. CARROLL ◽  
R. N. STILLWELL ◽  
E. C. HORNING

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