Unusual solvent effects in the reactions of 1-halo-2,4-dinitrobenzenes andaniline in aprotic and dipolar-aprotic solvents. Effects of aggregates

The kinetics of reactions between 1-halogeno-2,4-dinitrobenzene (halogen = F, Cl) and aniline were studied in toluene, acetone, dimethylsulfoxide and in toluene-acetone mixtures. Unexpectedly, when chlorine is the nucleofugue, the second rate coefficients, kA, in toluene shows a parabolic dependence...

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Autores principales: Alvaro, C.E.S., Nudelman, N.S.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_14246376_v2003_n10_p95_Alvaro
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spelling todo:paper_14246376_v2003_n10_p95_Alvaro2023-10-03T16:13:39Z Unusual solvent effects in the reactions of 1-halo-2,4-dinitrobenzenes andaniline in aprotic and dipolar-aprotic solvents. Effects of aggregates Alvaro, C.E.S. Nudelman, N.S. Aprotic solvents Aromatic nucleophilic substitutions Dimer nucleophile mechanism Mixed aggregates 1 chloro 2,4 dinitrobenzene 1 fluoro 2,4 dinitrobenzene acetone amine aniline chlorine dimer dimethyl sulfoxide fluorine toluene addition reaction article chemical reaction concentration (parameters) dimerization kinetics solvent effect substitution reaction The kinetics of reactions between 1-halogeno-2,4-dinitrobenzene (halogen = F, Cl) and aniline were studied in toluene, acetone, dimethylsulfoxide and in toluene-acetone mixtures. Unexpectedly, when chlorine is the nucleofugue, the second rate coefficients, kA, in toluene shows a parabolic dependence on the amine concentration which indicates a third order in amine kinetic law, while in the dipolar aprotic solvent the dependence is linear. Small additions of acetone to the solvent produce an important increase in rate, much greater then the increase in the permittivity, which is surprising on the basis of the classical effect of a dipolar medium on a dipolar transition state. The reactions with fluorine as the nucleofugue show similar behaviours. All these results are well explained in the frame of the "dimer nucleophile" mechanism. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_14246376_v2003_n10_p95_Alvaro
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Aprotic solvents
Aromatic nucleophilic substitutions
Dimer nucleophile mechanism
Mixed aggregates
1 chloro 2,4 dinitrobenzene
1 fluoro 2,4 dinitrobenzene
acetone
amine
aniline
chlorine
dimer
dimethyl sulfoxide
fluorine
toluene
addition reaction
article
chemical reaction
concentration (parameters)
dimerization
kinetics
solvent effect
substitution reaction
spellingShingle Aprotic solvents
Aromatic nucleophilic substitutions
Dimer nucleophile mechanism
Mixed aggregates
1 chloro 2,4 dinitrobenzene
1 fluoro 2,4 dinitrobenzene
acetone
amine
aniline
chlorine
dimer
dimethyl sulfoxide
fluorine
toluene
addition reaction
article
chemical reaction
concentration (parameters)
dimerization
kinetics
solvent effect
substitution reaction
Alvaro, C.E.S.
Nudelman, N.S.
Unusual solvent effects in the reactions of 1-halo-2,4-dinitrobenzenes andaniline in aprotic and dipolar-aprotic solvents. Effects of aggregates
topic_facet Aprotic solvents
Aromatic nucleophilic substitutions
Dimer nucleophile mechanism
Mixed aggregates
1 chloro 2,4 dinitrobenzene
1 fluoro 2,4 dinitrobenzene
acetone
amine
aniline
chlorine
dimer
dimethyl sulfoxide
fluorine
toluene
addition reaction
article
chemical reaction
concentration (parameters)
dimerization
kinetics
solvent effect
substitution reaction
description The kinetics of reactions between 1-halogeno-2,4-dinitrobenzene (halogen = F, Cl) and aniline were studied in toluene, acetone, dimethylsulfoxide and in toluene-acetone mixtures. Unexpectedly, when chlorine is the nucleofugue, the second rate coefficients, kA, in toluene shows a parabolic dependence on the amine concentration which indicates a third order in amine kinetic law, while in the dipolar aprotic solvent the dependence is linear. Small additions of acetone to the solvent produce an important increase in rate, much greater then the increase in the permittivity, which is surprising on the basis of the classical effect of a dipolar medium on a dipolar transition state. The reactions with fluorine as the nucleofugue show similar behaviours. All these results are well explained in the frame of the "dimer nucleophile" mechanism.
format JOUR
author Alvaro, C.E.S.
Nudelman, N.S.
author_facet Alvaro, C.E.S.
Nudelman, N.S.
author_sort Alvaro, C.E.S.
title Unusual solvent effects in the reactions of 1-halo-2,4-dinitrobenzenes andaniline in aprotic and dipolar-aprotic solvents. Effects of aggregates
title_short Unusual solvent effects in the reactions of 1-halo-2,4-dinitrobenzenes andaniline in aprotic and dipolar-aprotic solvents. Effects of aggregates
title_full Unusual solvent effects in the reactions of 1-halo-2,4-dinitrobenzenes andaniline in aprotic and dipolar-aprotic solvents. Effects of aggregates
title_fullStr Unusual solvent effects in the reactions of 1-halo-2,4-dinitrobenzenes andaniline in aprotic and dipolar-aprotic solvents. Effects of aggregates
title_full_unstemmed Unusual solvent effects in the reactions of 1-halo-2,4-dinitrobenzenes andaniline in aprotic and dipolar-aprotic solvents. Effects of aggregates
title_sort unusual solvent effects in the reactions of 1-halo-2,4-dinitrobenzenes andaniline in aprotic and dipolar-aprotic solvents. effects of aggregates
url http://hdl.handle.net/20.500.12110/paper_14246376_v2003_n10_p95_Alvaro
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AT nudelmanns unusualsolventeffectsinthereactionsof1halo24dinitrobenzenesandanilineinaproticanddipolaraproticsolventseffectsofaggregates
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