Publication
Title
Potentiometric, calorimetric and nuclear magnetic resonance studies of the protonation in aqueous solution of 1-thia-4,7-diazacyclononane-N,N'-diacetic acid, 1-thia-4,8-diazacyclononane-N,N'-diacetic acid and related open-chain diaminocarboxylic acids
Author
Abstract
The acid-base properties in aqueous solution of 1-thia-4,7-diazacyclononane -N,N-diacetic acid (TNODA) and 1-thia-4,8-diazacyclodecane-N,N-diacetic acid (TDEDA) have been investigated in 0.1 mol dm−3 KNO3 at 25C. The protonation constants were determined by conventional pH potentiometry. The protonation enthalpy changes were obtained by adiabatic calorimetry. The corresponding entropy changes were calculated. For TNODA: log KH1 = 11.63, log KH2 = 4.05, log KH3 = 1.8; ¢H1 = −41.4 kJ mol−1, ¢H2 = −0.5 kJ mol−1, ¢H3 = 4.2 kJ mol−1; ¢S1 = 83.5 J mol−1 K−1, ¢S2 = 75.8 J mol−1 K−1, ¢S3 = 48.5 J mol−1 K−1. For TDEDA: log KH1 = 12.9, log KH2 = 3.95, log KH3 = 2.0; ¢H2 = 0.2 kJ mol−1, ¢H3 = 3.2 kJ mol−1; ¢S2 = 76.2 J mol−1 K−1, ¢S3 = 50 J mol−1 K−1. The protonation sequence of the cyclic diaminocarboxylates was established by 1H NMR spectroscopy. The results indicate that the first proton is added to a tertiary amino group, whereas the second and the third are added to the two carboxylate groups. The second amino group of TDEDA is only protonated in strong acid medium. Reduced solvation of the cyclic diaminocarboxylates as compared with their open-chain counterparts explains the increase in basicity at the first protonation step upon acetate substitution on the second amino group of the parent cyclic diamines. The acid-base properties of the open-chain diaminocarboxylates 2,5-diazahexane-N,N-diacetic acid and 5-thia-2,8-diazanonene-N,N-diacetic acid were also investigated under the same experimental conditions for comparison purposes.
Language
English
Source (journal)
Polyhedron. - Oxford
Publication
Oxford : 1992
ISSN
0277-5387
Volume/pages
11:11(1992), p. 1305-1313
ISI
A1992HZ85800003
Full text (Publisher's DOI)
UAntwerpen
Faculty/Department
Publication type
Subject
External links
Web of Science
Record
Identification
Creation 27.09.2013
Last edited 01.07.2017