Analysis of reaction products formed in the gas phase reaction of E,E-2,4-hexadienal with atmospheric oxidants: Reaction mechanisms and atmospheric implications

2018 ◽  
Vol 176 ◽  
pp. 188-200 ◽  
Author(s):  
I. Colmenar ◽  
P. Martin ◽  
B. Cabañas ◽  
S. Salgado ◽  
E. Martinez
2015 ◽  
Vol 122 ◽  
pp. 513-520 ◽  
Author(s):  
Jason E. Ham ◽  
Stephen R. Jackson ◽  
Joel C. Harrison ◽  
J.R. Wells

1995 ◽  
Vol 11 (4) ◽  
pp. 683-697 ◽  
Author(s):  
R. A. Yetter ◽  
F. L. Dryer ◽  
M. T. Allen ◽  
J. L. Gatto

2009 ◽  
Vol 08 (06) ◽  
pp. 1217-1226 ◽  
Author(s):  
JUN CAI ◽  
ZHIJIAN WU

Intramolecular amide hydrolysis of N-methylmaleamic acid is revisited at the B3LYP/6-311G(2df, p)//B3LYP/6-31G(d, p) + ZVPE level, including solvent effects at the CPCM-B3LYP/6-311G(2df, p)//Onsager-B3LYP/6-31G(d, p) + ZPVE level. The concerted reaction mechanism is energetically favorable over stepwise reaction mechanisms in both the gas phase and solution. The calculated reaction barriers are significantly lower in solution than in the gas phase. In addition, it is concluded that the substituents of the four N-methylmaleamic acid derivatives considered herein have a significant effect on the gas-phase reaction barriers but a smaller, or little, effect on the barriers in solution.


2016 ◽  
Vol 132 ◽  
pp. 300-308 ◽  
Author(s):  
Jason E. Ham ◽  
Joel C. Harrison ◽  
Stephen R. Jackson ◽  
J.R. Wells

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