US EPA

7855849 

Journal Article 

The mechanism of aromatic nucleophilic substitution reaction between ethanolamine and fluoro-nitrobenzenes: an investigation by kinetic measurements and DFT calculations 

Jose, KB; Cyriac, J; Moolayil, JT; Sebastian, VS; George, M 

2011 

Yes 

Journal of Physical Organic Chemistry
ISSN: 0894-3230 

WILEY 

HOBOKEN 

24 

8 

714-719 

English 

10.1002/poc.1817 

WOS:000293594100014 

We have studied the kinetics and elucidated the mechanism by DFT calculation of the reaction between ethanolamine (EOA) and 1-fluoro-2,4- dinitrobenzene (DNFB) in acetonitrile and toluene. To determine the contribution of the nitro group, the activation energy of the reaction between ethanolamine and 1-fluoro-2-nitrobenzene (MNFB) vs. DNFB was determined in acetonitrile and calculated by DFT method. Kinetic measurements reveal that the reaction is faster in acetonitrile than in toluene. The reaction follows overall second-order kinetics: first order with respect to both EOA and DNFB which is similar to the results reported for reaction between other primary amines and 1-substituted-2,4-dinitrobenzenes. The calculations by using DFT methods reveal that the mechanism of the reaction involves the formation and decomposition of a Meisenheimer complex (MC). DFT calculations also reveal that the activation energy of the reaction is highest in vacuum and decreases with increasing polarity of the solvent reaching a minimum in acetonitrile. In addition, activation energies obtained by both DFT calculations and experiments show that the reactivity of MNFB is less than that of DNFB showing the effect of the 4-nitro group. © 2010 John Wiley & Sons, Ltd. 

activation energy; aromatic nucleophilic substitution; DFT calculation; Meisenheimer complex; solvent effects