Phenolic Acids Ozonation: QSAR Analysis and pH Influence on the Selectivity of Ozone

2009 ◽  
Vol 12 (2) ◽  
Author(s):  
Joaquín R. Domínguez ◽  
José A. Peres ◽  
Jesús Beltran-Heredia

AbstractOzone reacts selectively with ortho-, meta- and para- substituted phenolic acids in aqueous solution. Analysis of second-order rate constants for correlations reveals quantitative structure-activity relationships (QSARs). The kinetic rate constants for oxidation of these phenolic acids were correlated to Hammett-substituent-electronic constant. The values of Hammett parameter ρ varying between -2.9 and -0.3 were found for different pH conditions. The pH influence on this parameter reveals the expected change in the ozonation mechanism due to the decomposition of ozone generating hydroxyl radicals. Contrarily, hydroxyl radicals are non-selective and the substituent-electronic effects are small. This Hammett’s study reflects the progressive change in the selectivity of the oxidation system when the pH increases from 2 up to 9.

Biochemistry ◽  
1991 ◽  
Vol 30 (29) ◽  
pp. 7283-7297 ◽  
Author(s):  
Otto G. Berg ◽  
Bao Zhu Yu ◽  
Joe Rogers ◽  
Mahendra Kumar Jain

1998 ◽  
Vol 217 (1-2) ◽  
pp. 51-60 ◽  
Author(s):  
Claire L. Morgan ◽  
David J. Newman ◽  
Jacky M. Burrin ◽  
Christopher P. Price

2019 ◽  
Vol 21 (32) ◽  
pp. 17760-17771 ◽  
Author(s):  
Gustavo J. R. Aroeira ◽  
Adam S. Abbott ◽  
Sarah N. Elliott ◽  
Justin M. Turney ◽  
Henry F. Schaefer

High level ab initio methods are employed to study the addition of methanol to the simplest Criegee intermediates and its methylated analogue. Kinetic rate constants over a range of temperatures are computed and compared to experimental results.


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