Base hydrolysis and aquation of trans-methyl-substituted acidopenta-amminecobalt(III) complexes

Base hydrolysis and aquation of trans-[Co(NH₃)₄(NH₂CH₃)X]²⁺ (where X = Cl, Br and NO3) complexes are reported. Both types of reactions are four to eight times faster than the corresponding reactions for [Co(NH3)5X]2+ complexes. The positive activation entropies of the base hydrolysis for all the stu...

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Autores principales: Benzo, Fabián, Massaferro, Adriana, Queirolo, Marcelo, Sienra, Beatriz, Capparelli, Alberto Luis, Mártire, Daniel Osvaldo
Formato: Articulo
Lenguaje:Inglés
Publicado: 1996
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/159209
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id I19-R120-10915-159209
record_format dspace
spelling I19-R120-10915-1592092023-10-23T20:46:22Z http://sedici.unlp.edu.ar/handle/10915/159209 Base hydrolysis and aquation of trans-methyl-substituted acidopenta-amminecobalt(III) complexes Benzo, Fabián Massaferro, Adriana Queirolo, Marcelo Sienra, Beatriz Capparelli, Alberto Luis Mártire, Daniel Osvaldo 1996 2023-10-23T13:43:52Z en Química Base hydrolysis aquation reactions activation entropies Base hydrolysis and aquation of trans-[Co(NH₃)₄(NH₂CH₃)X]²⁺ (where X = Cl, Br and NO3) complexes are reported. Both types of reactions are four to eight times faster than the corresponding reactions for [Co(NH3)5X]2+ complexes. The positive activation entropies of the base hydrolysis for all the studied trans-[Co(NH₃)₄(NH₂CH₃)X]²⁺ ions and the stereochemistry of the hydroxo products are indicative of a dissociative conjugate base, Dcb, mechanism. The steric course of the base hydrolysis differs significantly from that of the parent penta-ammines. For the aquation reactions, the activation enthalpies of the trans-methylamine and penta-ammine complexes are similar, while the activation entropies are more positive (or less negative) for the former. These results are interpreted in terms of an Id mechanism. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas Articulo Articulo http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) application/pdf 1915-1921
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Química
Base hydrolysis
aquation reactions
activation entropies
spellingShingle Química
Base hydrolysis
aquation reactions
activation entropies
Benzo, Fabián
Massaferro, Adriana
Queirolo, Marcelo
Sienra, Beatriz
Capparelli, Alberto Luis
Mártire, Daniel Osvaldo
Base hydrolysis and aquation of trans-methyl-substituted acidopenta-amminecobalt(III) complexes
topic_facet Química
Base hydrolysis
aquation reactions
activation entropies
description Base hydrolysis and aquation of trans-[Co(NH₃)₄(NH₂CH₃)X]²⁺ (where X = Cl, Br and NO3) complexes are reported. Both types of reactions are four to eight times faster than the corresponding reactions for [Co(NH3)5X]2+ complexes. The positive activation entropies of the base hydrolysis for all the studied trans-[Co(NH₃)₄(NH₂CH₃)X]²⁺ ions and the stereochemistry of the hydroxo products are indicative of a dissociative conjugate base, Dcb, mechanism. The steric course of the base hydrolysis differs significantly from that of the parent penta-ammines. For the aquation reactions, the activation enthalpies of the trans-methylamine and penta-ammine complexes are similar, while the activation entropies are more positive (or less negative) for the former. These results are interpreted in terms of an Id mechanism.
format Articulo
Articulo
author Benzo, Fabián
Massaferro, Adriana
Queirolo, Marcelo
Sienra, Beatriz
Capparelli, Alberto Luis
Mártire, Daniel Osvaldo
author_facet Benzo, Fabián
Massaferro, Adriana
Queirolo, Marcelo
Sienra, Beatriz
Capparelli, Alberto Luis
Mártire, Daniel Osvaldo
author_sort Benzo, Fabián
title Base hydrolysis and aquation of trans-methyl-substituted acidopenta-amminecobalt(III) complexes
title_short Base hydrolysis and aquation of trans-methyl-substituted acidopenta-amminecobalt(III) complexes
title_full Base hydrolysis and aquation of trans-methyl-substituted acidopenta-amminecobalt(III) complexes
title_fullStr Base hydrolysis and aquation of trans-methyl-substituted acidopenta-amminecobalt(III) complexes
title_full_unstemmed Base hydrolysis and aquation of trans-methyl-substituted acidopenta-amminecobalt(III) complexes
title_sort base hydrolysis and aquation of trans-methyl-substituted acidopenta-amminecobalt(iii) complexes
publishDate 1996
url http://sedici.unlp.edu.ar/handle/10915/159209
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AT sienrabeatriz basehydrolysisandaquationoftransmethylsubstitutedacidopentaamminecobaltiiicomplexes
AT capparellialbertoluis basehydrolysisandaquationoftransmethylsubstitutedacidopentaamminecobaltiiicomplexes
AT martiredanielosvaldo basehydrolysisandaquationoftransmethylsubstitutedacidopentaamminecobaltiiicomplexes
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