The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profiles

Detalhes bibliográficos
Autor(a) principal: Brighente,Inês Maria Costa
Data de Publicação: 1997
Outros Autores: Yunes,Rosendo Augusto
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531997000500018
Resumo: It have been described a general mechanism for the attack step of the reactions between nitrogen nucleophiles and carbonyl compounds to form a neutral tetrahedral addition intermediate. This general mechanism is based on the relative importance of the "concerted" hydronium-ion catalyzed attack of the nitrogen base on the carbonyl compound with respect to the "step wise" mechanism that involves the previous formation of a zwitterionic tetrahedral intermediate (T±) and the posterior proton transfer to it from the hydronium-ion. The relative importance of this pathway gives origin to three kinds of profile rates vs pH for these reactions. On the other hand, the importance of the "stepwise" mechanism was attributed to a dependence on the stability of the T± intermediate that is related to the pKa of the nitrogen base and the Kad (the equilibrium constant for the formation of the neutral tetrahedral addition intermediate (T0)). The comparison of the reactions of p-chlorobenzaldehyde and norcamphor with different nitrogen nucleophiles led to the observation that the general mechanism depends on each type of carbonyl compound. This is due to the great influence of the steric and electronic effects of the compounds structure, and the fact that the pKa value of the nitrogen base, which is more related to the stability of the T± than the T0 intermediate, is more important as a factor of prediction of the profiles than the value of Kad, this value being more related to the stability of the T0 intermediate.
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spelling The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profilescarbonyl compoundsnitrogen nucleophilesgeneral mechanism of attackIt have been described a general mechanism for the attack step of the reactions between nitrogen nucleophiles and carbonyl compounds to form a neutral tetrahedral addition intermediate. This general mechanism is based on the relative importance of the "concerted" hydronium-ion catalyzed attack of the nitrogen base on the carbonyl compound with respect to the "step wise" mechanism that involves the previous formation of a zwitterionic tetrahedral intermediate (T±) and the posterior proton transfer to it from the hydronium-ion. The relative importance of this pathway gives origin to three kinds of profile rates vs pH for these reactions. On the other hand, the importance of the "stepwise" mechanism was attributed to a dependence on the stability of the T± intermediate that is related to the pKa of the nitrogen base and the Kad (the equilibrium constant for the formation of the neutral tetrahedral addition intermediate (T0)). The comparison of the reactions of p-chlorobenzaldehyde and norcamphor with different nitrogen nucleophiles led to the observation that the general mechanism depends on each type of carbonyl compound. This is due to the great influence of the steric and electronic effects of the compounds structure, and the fact that the pKa value of the nitrogen base, which is more related to the stability of the T± than the T0 intermediate, is more important as a factor of prediction of the profiles than the value of Kad, this value being more related to the stability of the T0 intermediate.Sociedade Brasileira de Química1997-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531997000500018Journal of the Brazilian Chemical Society v.8 n.5 1997reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50531997000500018info:eu-repo/semantics/openAccessBrighente,Inês Maria CostaYunes,Rosendo Augustoeng2010-09-10T00:00:00Zoai:scielo:S0103-50531997000500018Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2010-09-10T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profiles
title The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profiles
spellingShingle The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profiles
Brighente,Inês Maria Costa
carbonyl compounds
nitrogen nucleophiles
general mechanism of attack
title_short The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profiles
title_full The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profiles
title_fullStr The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profiles
title_full_unstemmed The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profiles
title_sort The general mechanisms of attack of nitrogen nucleophiles on carbonyl compounds: facts that determine the change of the rate-pH profiles
author Brighente,Inês Maria Costa
author_facet Brighente,Inês Maria Costa
Yunes,Rosendo Augusto
author_role author
author2 Yunes,Rosendo Augusto
author2_role author
dc.contributor.author.fl_str_mv Brighente,Inês Maria Costa
Yunes,Rosendo Augusto
dc.subject.por.fl_str_mv carbonyl compounds
nitrogen nucleophiles
general mechanism of attack
topic carbonyl compounds
nitrogen nucleophiles
general mechanism of attack
description It have been described a general mechanism for the attack step of the reactions between nitrogen nucleophiles and carbonyl compounds to form a neutral tetrahedral addition intermediate. This general mechanism is based on the relative importance of the "concerted" hydronium-ion catalyzed attack of the nitrogen base on the carbonyl compound with respect to the "step wise" mechanism that involves the previous formation of a zwitterionic tetrahedral intermediate (T±) and the posterior proton transfer to it from the hydronium-ion. The relative importance of this pathway gives origin to three kinds of profile rates vs pH for these reactions. On the other hand, the importance of the "stepwise" mechanism was attributed to a dependence on the stability of the T± intermediate that is related to the pKa of the nitrogen base and the Kad (the equilibrium constant for the formation of the neutral tetrahedral addition intermediate (T0)). The comparison of the reactions of p-chlorobenzaldehyde and norcamphor with different nitrogen nucleophiles led to the observation that the general mechanism depends on each type of carbonyl compound. This is due to the great influence of the steric and electronic effects of the compounds structure, and the fact that the pKa value of the nitrogen base, which is more related to the stability of the T± than the T0 intermediate, is more important as a factor of prediction of the profiles than the value of Kad, this value being more related to the stability of the T0 intermediate.
publishDate 1997
dc.date.none.fl_str_mv 1997-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531997000500018
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50531997000500018
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50531997000500018
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.8 n.5 1997
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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