Catalysis of Trans-esterification Reactions in Model Ester Mixtures

Model trans-esterification reaction of n-butylbenzoate with phenyl-p-chlorobenzoate in the molar ratio of 20:1 has been studied. In order to evaluate catalysts based on lanthanide system the activity of nyodymium compounds – neodymium acetate, neodymium acetylacetonate and nitrate complex with benzo...

Full description

Bibliographic Details
Main Authors: V. A. Vasnev, G. D. Markova, B. A. Uvarov, W. Yu. Voytekunas, M. J.M. Abadie
Format: Article
Language:English
Published: al-Farabi Kazakh National University 2005-04-01
Series:Eurasian Chemico-Technological Journal
Online Access:http://ect-journal.kz/index.php/ectj/article/view/543
_version_ 1818791542477815808
author V. A. Vasnev
G. D. Markova
B. A. Uvarov
W. Yu. Voytekunas
M. J.M. Abadie
author_facet V. A. Vasnev
G. D. Markova
B. A. Uvarov
W. Yu. Voytekunas
M. J.M. Abadie
author_sort V. A. Vasnev
collection DOAJ
description Model trans-esterification reaction of n-butylbenzoate with phenyl-p-chlorobenzoate in the molar ratio of 20:1 has been studied. In order to evaluate catalysts based on lanthanide system the activity of nyodymium compounds – neodymium acetate, neodymium acetylacetonate and nitrate complex with benzo-12-crown-4 (neodymium nitrate coronate) – has been studied in the model trans-esterification reaction of n-butylbenzoate with phenyl-pchlorobenzoate. The effect of the electronic structure of the metal on the catalytic activity of the coronates of lanthanum, cerium, praseodymium, neodymium, samarium, terbium and erbium nitrates has been studied. In order to estimate the optimum concentration of the catalysts, a study of the dependence of the transesterification reaction on concentration of neodymium nitrate coronate was carried out. An asymptotic nature of the concentration dependence on the catalytic activity of lanthanide compounds has been observed. In order to look for new classes of inhibitors of trans-esterefication reaction, the model trans-esterificatiom reaction of n-butylbenzoate with phenyl-p-chlorbenzoate has been studied in the presence of some carborane derivatives: cesium salts of bis-1,2-(dicarbollyl) complexes of iron, cobalt and nickel(3+) and bis-1,2(dicarbollyl) nickel(4+) [(C2B9H11)2Me]. Some of these compounds were found to be effective inhibitors. The dependence of the constant rate of the model trans-esterification reaction of n-butylbenzoate with phenyl-p-chlorobenzoate on the concentration of cerium salt of bis-1,2-(dicarbollyl) complex of nickel has been studied to determine the optimum concentration of inhibitors. The influence of the ester chemical structure on the activity of ester groups in the trans-esterification activity has been determined in the reaction of di-n-butylterephthalate with different p-substituted derivatives of phenylbenzoate (phenyl-p-methoxybenzoate, phenyl-p-methylbenzoate, phenylbenzoate, phenyl- pchlorobenzoate, phenyl-p-nitrobenzoate, p-methoxyphenylbenzoate, p-methylphenylbenzoate, p-chlorophenylbenzoate, p-nitrophenylbenzoate, n-butylbenzoate, di-n-butylterephthalate) in presence of the samarium nitrate coronate.
first_indexed 2024-12-18T15:13:00Z
format Article
id doaj.art-37d2b6e1f0d84c968e72b42fd0e22fe7
institution Directory Open Access Journal
issn 1562-3920
2522-4867
language English
last_indexed 2024-12-18T15:13:00Z
publishDate 2005-04-01
publisher al-Farabi Kazakh National University
record_format Article
series Eurasian Chemico-Technological Journal
spelling doaj.art-37d2b6e1f0d84c968e72b42fd0e22fe72022-12-21T21:03:36Zengal-Farabi Kazakh National UniversityEurasian Chemico-Technological Journal1562-39202522-48672005-04-0172798410.18321/ectj618543Catalysis of Trans-esterification Reactions in Model Ester MixturesV. A. Vasnev0G. D. Markova1B. A. Uvarov2W. Yu. Voytekunas3M. J.M. Abadie4A.N. Nesmeyanov Institute of Organo-Element Compounds - INEOS, Russian Academy of Science, 28 Vavilov str., Moscow, 117813, RussiaA.N. Nesmeyanov Institute of Organo-Element Compounds - INEOS, Russian Academy of Science, 28 Vavilov str., Moscow, 117813, RussiaA.N. Nesmeyanov Institute of Organo-Element Compounds - INEOSLaboratory of Polymer Science & Advanced Organic Materials – LEMP/MAO – Université Montpellier 2, Sciences et Techniques du Languedoc, Place Bataillon, 34095 Montpellier Cedex 05, FranceLaboratory of Polymer Science & Advanced Organic Materials – LEMP/MAO – Université Montpellier 2, Sciences et Techniques du Languedoc, Place Bataillon, 34095 Montpellier Cedex 05, FranceModel trans-esterification reaction of n-butylbenzoate with phenyl-p-chlorobenzoate in the molar ratio of 20:1 has been studied. In order to evaluate catalysts based on lanthanide system the activity of nyodymium compounds – neodymium acetate, neodymium acetylacetonate and nitrate complex with benzo-12-crown-4 (neodymium nitrate coronate) – has been studied in the model trans-esterification reaction of n-butylbenzoate with phenyl-pchlorobenzoate. The effect of the electronic structure of the metal on the catalytic activity of the coronates of lanthanum, cerium, praseodymium, neodymium, samarium, terbium and erbium nitrates has been studied. In order to estimate the optimum concentration of the catalysts, a study of the dependence of the transesterification reaction on concentration of neodymium nitrate coronate was carried out. An asymptotic nature of the concentration dependence on the catalytic activity of lanthanide compounds has been observed. In order to look for new classes of inhibitors of trans-esterefication reaction, the model trans-esterificatiom reaction of n-butylbenzoate with phenyl-p-chlorbenzoate has been studied in the presence of some carborane derivatives: cesium salts of bis-1,2-(dicarbollyl) complexes of iron, cobalt and nickel(3+) and bis-1,2(dicarbollyl) nickel(4+) [(C2B9H11)2Me]. Some of these compounds were found to be effective inhibitors. The dependence of the constant rate of the model trans-esterification reaction of n-butylbenzoate with phenyl-p-chlorobenzoate on the concentration of cerium salt of bis-1,2-(dicarbollyl) complex of nickel has been studied to determine the optimum concentration of inhibitors. The influence of the ester chemical structure on the activity of ester groups in the trans-esterification activity has been determined in the reaction of di-n-butylterephthalate with different p-substituted derivatives of phenylbenzoate (phenyl-p-methoxybenzoate, phenyl-p-methylbenzoate, phenylbenzoate, phenyl- pchlorobenzoate, phenyl-p-nitrobenzoate, p-methoxyphenylbenzoate, p-methylphenylbenzoate, p-chlorophenylbenzoate, p-nitrophenylbenzoate, n-butylbenzoate, di-n-butylterephthalate) in presence of the samarium nitrate coronate.http://ect-journal.kz/index.php/ectj/article/view/543
spellingShingle V. A. Vasnev
G. D. Markova
B. A. Uvarov
W. Yu. Voytekunas
M. J.M. Abadie
Catalysis of Trans-esterification Reactions in Model Ester Mixtures
Eurasian Chemico-Technological Journal
title Catalysis of Trans-esterification Reactions in Model Ester Mixtures
title_full Catalysis of Trans-esterification Reactions in Model Ester Mixtures
title_fullStr Catalysis of Trans-esterification Reactions in Model Ester Mixtures
title_full_unstemmed Catalysis of Trans-esterification Reactions in Model Ester Mixtures
title_short Catalysis of Trans-esterification Reactions in Model Ester Mixtures
title_sort catalysis of trans esterification reactions in model ester mixtures
url http://ect-journal.kz/index.php/ectj/article/view/543
work_keys_str_mv AT vavasnev catalysisoftransesterificationreactionsinmodelestermixtures
AT gdmarkova catalysisoftransesterificationreactionsinmodelestermixtures
AT bauvarov catalysisoftransesterificationreactionsinmodelestermixtures
AT wyuvoytekunas catalysisoftransesterificationreactionsinmodelestermixtures
AT mjmabadie catalysisoftransesterificationreactionsinmodelestermixtures