A study of the behaviour of some substituted 1,2,4-triazoline-3-thiones in different media

The acid-base behaviour of 4-phenyl-5-(4-R-benzyl)-1,2,4-triazoline-3-thione (1(R = OH); 2(R = OC2H5)) was studied in aqueous sulfuric acid and sodium hydroxide solutions. Three ionisation equilibria of compound 1 (pKBH3+ = 4.64, pKBH2 = 7.50, pKBH = 10.06) and two ionisation equilibria of compound...

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Main Authors: MARIJA LAZAREVIC, LUCIJANA ARMAN-ZUBIC, NADA PERISIC-JANJIC
Format: Article
Language:English
Published: Serbian Chemical Society 2000-09-01
Series:Journal of the Serbian Chemical Society
Subjects:
Online Access:http://www.shd.org.yu/HtDocs/SHD/Vol65/No9-Pdf/JSCS9-02.pdf
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author MARIJA LAZAREVIC
LUCIJANA ARMAN-ZUBIC
NADA PERISIC-JANJIC
author_facet MARIJA LAZAREVIC
LUCIJANA ARMAN-ZUBIC
NADA PERISIC-JANJIC
author_sort MARIJA LAZAREVIC
collection DOAJ
description The acid-base behaviour of 4-phenyl-5-(4-R-benzyl)-1,2,4-triazoline-3-thione (1(R = OH); 2(R = OC2H5)) was studied in aqueous sulfuric acid and sodium hydroxide solutions. Three ionisation equilibria of compound 1 (pKBH3+ = 4.64, pKBH2 = 7.50, pKBH = 10.06) and two ionisation equilibria of compound 2 (pKBH2+ = 4.82, pKBH = 7.45) were found. The first equilibrium belongs to the protonation of 1,2,4-triazoline-3-thione, while the second belongs to the dissociation of the same part of the molecule. The third equilibrium represents the dissociation process of the phenolic OH group of compound 1. The kinetics of hydrolysis of compounds 1 and 2 were studied in high concentrated sulfuric acid solutions. The hydrolysis follows an irreversible first-order consecutive reaction path.
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spelling doaj.art-f8de8c2b04124a0888e6879b09a8c0e62022-12-22T01:36:08ZengSerbian Chemical SocietyJournal of the Serbian Chemical Society0352-51392000-09-01659619630A study of the behaviour of some substituted 1,2,4-triazoline-3-thiones in different mediaMARIJA LAZAREVICLUCIJANA ARMAN-ZUBICNADA PERISIC-JANJICThe acid-base behaviour of 4-phenyl-5-(4-R-benzyl)-1,2,4-triazoline-3-thione (1(R = OH); 2(R = OC2H5)) was studied in aqueous sulfuric acid and sodium hydroxide solutions. Three ionisation equilibria of compound 1 (pKBH3+ = 4.64, pKBH2 = 7.50, pKBH = 10.06) and two ionisation equilibria of compound 2 (pKBH2+ = 4.82, pKBH = 7.45) were found. The first equilibrium belongs to the protonation of 1,2,4-triazoline-3-thione, while the second belongs to the dissociation of the same part of the molecule. The third equilibrium represents the dissociation process of the phenolic OH group of compound 1. The kinetics of hydrolysis of compounds 1 and 2 were studied in high concentrated sulfuric acid solutions. The hydrolysis follows an irreversible first-order consecutive reaction path.http://www.shd.org.yu/HtDocs/SHD/Vol65/No9-Pdf/JSCS9-02.pdf124-triazoline-3-thione derivativeselectonic absorption spectradissociation constantsacid hydrolysis
spellingShingle MARIJA LAZAREVIC
LUCIJANA ARMAN-ZUBIC
NADA PERISIC-JANJIC
A study of the behaviour of some substituted 1,2,4-triazoline-3-thiones in different media
Journal of the Serbian Chemical Society
1
2
4-triazoline-3-thione derivatives
electonic absorption spectra
dissociation constants
acid hydrolysis
title A study of the behaviour of some substituted 1,2,4-triazoline-3-thiones in different media
title_full A study of the behaviour of some substituted 1,2,4-triazoline-3-thiones in different media
title_fullStr A study of the behaviour of some substituted 1,2,4-triazoline-3-thiones in different media
title_full_unstemmed A study of the behaviour of some substituted 1,2,4-triazoline-3-thiones in different media
title_short A study of the behaviour of some substituted 1,2,4-triazoline-3-thiones in different media
title_sort study of the behaviour of some substituted 1 2 4 triazoline 3 thiones in different media
topic 1
2
4-triazoline-3-thione derivatives
electonic absorption spectra
dissociation constants
acid hydrolysis
url http://www.shd.org.yu/HtDocs/SHD/Vol65/No9-Pdf/JSCS9-02.pdf
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