Cargando…

Kinetics and Mechanisms of the Chromium(III) Reactions with 2,4- and 2,5-Dihydroxybenzoic Acids in Weak Acidic Aqueous Solutions

The reactions of 2,4- and 2,5-dihydroxybenzoic acids (dihydroxybenzoic acid, DHBA) with chromium(III) in weak acidic aqueous solutions have been shown to take place in at least two stages. The first stage of the reactions has an observed rate constant k (1(obs)) = k (1)[DHBA] + C and the correspondi...

Descripción completa

Detalles Bibliográficos
Autores principales: Zavitsanos, Kimon, Petrou, Athinoula L.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2913840/
https://www.ncbi.nlm.nih.gov/pubmed/20721282
http://dx.doi.org/10.1155/2010/832768
_version_ 1782184697359499264
author Zavitsanos, Kimon
Petrou, Athinoula L.
author_facet Zavitsanos, Kimon
Petrou, Athinoula L.
author_sort Zavitsanos, Kimon
collection PubMed
description The reactions of 2,4- and 2,5-dihydroxybenzoic acids (dihydroxybenzoic acid, DHBA) with chromium(III) in weak acidic aqueous solutions have been shown to take place in at least two stages. The first stage of the reactions has an observed rate constant k (1(obs)) = k (1)[DHBA] + C and the corresponding activation parameters are ΔH(1(2,4)) (≠) = 49, 5 kJ/mol(−1), ΔS (1(2,4)) (≠) = −103, 7 J mol(−1) K(−1), ΔH(1(2,5)) (≠) = 60, 3 kJ/mol(−1), and ΔS (1(2,5)) (≠) = −68, 0 J mol(−1) K(−1). These are composite activation parameters and the breaking of the strong intramolecular hydrogen bonding in the two ligands is suggested to be the first step of the (composite) first stage of the reactions. The second stage is ligand concentration independent and is thus attributed to a chelation process. The corresponding activation parameters are ΔH(2(2,4)) (≠) = 45, 13 kJ/mol(−1), ΔS (2(2,4)) (≠) = −185, 9 J mol(−1) K(−1), ΔH(2(2,5)) (≠) = 54, 55 kJ/mol(−1), and ΔS (2(2,5)) (≠) = −154, 8 J mol(−1) K(−1). The activation parameters support an associative mechanism for the second stage of the reactions. The various substitution processes are accompanied by proton release, resulting in pH decrease.
format Text
id pubmed-2913840
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-29138402010-08-18 Kinetics and Mechanisms of the Chromium(III) Reactions with 2,4- and 2,5-Dihydroxybenzoic Acids in Weak Acidic Aqueous Solutions Zavitsanos, Kimon Petrou, Athinoula L. Bioinorg Chem Appl Research Article The reactions of 2,4- and 2,5-dihydroxybenzoic acids (dihydroxybenzoic acid, DHBA) with chromium(III) in weak acidic aqueous solutions have been shown to take place in at least two stages. The first stage of the reactions has an observed rate constant k (1(obs)) = k (1)[DHBA] + C and the corresponding activation parameters are ΔH(1(2,4)) (≠) = 49, 5 kJ/mol(−1), ΔS (1(2,4)) (≠) = −103, 7 J mol(−1) K(−1), ΔH(1(2,5)) (≠) = 60, 3 kJ/mol(−1), and ΔS (1(2,5)) (≠) = −68, 0 J mol(−1) K(−1). These are composite activation parameters and the breaking of the strong intramolecular hydrogen bonding in the two ligands is suggested to be the first step of the (composite) first stage of the reactions. The second stage is ligand concentration independent and is thus attributed to a chelation process. The corresponding activation parameters are ΔH(2(2,4)) (≠) = 45, 13 kJ/mol(−1), ΔS (2(2,4)) (≠) = −185, 9 J mol(−1) K(−1), ΔH(2(2,5)) (≠) = 54, 55 kJ/mol(−1), and ΔS (2(2,5)) (≠) = −154, 8 J mol(−1) K(−1). The activation parameters support an associative mechanism for the second stage of the reactions. The various substitution processes are accompanied by proton release, resulting in pH decrease. Hindawi Publishing Corporation 2010 2010-07-11 /pmc/articles/PMC2913840/ /pubmed/20721282 http://dx.doi.org/10.1155/2010/832768 Text en Copyright © 2010 K. Zavitsanos and A. L. Petrou. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zavitsanos, Kimon
Petrou, Athinoula L.
Kinetics and Mechanisms of the Chromium(III) Reactions with 2,4- and 2,5-Dihydroxybenzoic Acids in Weak Acidic Aqueous Solutions
title Kinetics and Mechanisms of the Chromium(III) Reactions with 2,4- and 2,5-Dihydroxybenzoic Acids in Weak Acidic Aqueous Solutions
title_full Kinetics and Mechanisms of the Chromium(III) Reactions with 2,4- and 2,5-Dihydroxybenzoic Acids in Weak Acidic Aqueous Solutions
title_fullStr Kinetics and Mechanisms of the Chromium(III) Reactions with 2,4- and 2,5-Dihydroxybenzoic Acids in Weak Acidic Aqueous Solutions
title_full_unstemmed Kinetics and Mechanisms of the Chromium(III) Reactions with 2,4- and 2,5-Dihydroxybenzoic Acids in Weak Acidic Aqueous Solutions
title_short Kinetics and Mechanisms of the Chromium(III) Reactions with 2,4- and 2,5-Dihydroxybenzoic Acids in Weak Acidic Aqueous Solutions
title_sort kinetics and mechanisms of the chromium(iii) reactions with 2,4- and 2,5-dihydroxybenzoic acids in weak acidic aqueous solutions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2913840/
https://www.ncbi.nlm.nih.gov/pubmed/20721282
http://dx.doi.org/10.1155/2010/832768
work_keys_str_mv AT zavitsanoskimon kineticsandmechanismsofthechromiumiiireactionswith24and25dihydroxybenzoicacidsinweakacidicaqueoussolutions
AT petrouathinoulal kineticsandmechanismsofthechromiumiiireactionswith24and25dihydroxybenzoicacidsinweakacidicaqueoussolutions