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Solvent effects on aromatic nucleophilic substitution reactions. Part 7. Determination of the empirical polarity parameter E T (30) for dipolar hydrogen bond acceptor–co‐solvent (chloroform or dichloromethane) mixtures. Kinetics of the reactions of halonitrobenzenes with aliphatic amines
Author(s) -
Mancini P. M. E.,
Terenzani A.,
Adam C.,
Vottero L. R.
Publication year - 1997
Publication title -
journal of physical organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.325
H-Index - 66
eISSN - 1099-1395
pISSN - 0894-3230
DOI - 10.1002/(sici)1099-1395(199711)10:11<849::aid-pca936>3.0.co;2-3
Subject(s) - chemistry , dichloromethane , chloroform , solvent , solvent polarity , solvent effects , kinetics , photochemistry , nucleophilic substitution , nucleophilic aromatic substitution , acceptor , nucleophile , hydrogen bond , substitution reaction , organic chemistry , computational chemistry , molecule , catalysis , physics , quantum mechanics , condensed matter physics
Empirical solvent polarity parameters E T (30) were determined by UV/VIS spectroscopy, using Dimroth–Reichardt's betaine dye, as a function of composition, for several binary solvent mixtures [i.e. polar hydrogen bond acceptor (PHBA) solvents+chloroform or dichloromethane]. Each solvent system was analyzed according to its deviations from additivity due to preferential solvation of the chemical probe and also from complicated intermolecular interactions of the mixed solvents. The E T (30) parameter of many of these mixtures has presented synergism. The synergetic effects were more significant for those binary solvent systems in which chloroform is the co‐solvent. These results were related to the solvent effects on some aromatic nucleophilic substitution reactions. The kinetics of the reactions between 1‐halo‐2,4‐dinitrobenzenes and primary or secondary aliphatic amines were studied in three solvent systems (PHBA+chloroform) where the synergism for the E T (30) polarity parameter is the rule. In all the aminodehalogenation reactions discussed the formation of the intermediate is the rate‐determining step. The kinetic data show a tendency to decrease with decrease in the overall solvation capability of the binary mixture. In general, the reaction rates presented a gradual decrease in the PHBA solvent‐rich zone and a large decrease at high co‐solvent concentrations. The E T (30) values corresponding to binary dipolar hydrogen bond acceptor–hydrogen bond donor mixtures may be not generally valid for interpreting solvation effects on the reactions under consideration. © 1997 John Wiley & Sons, Ltd.