IONIC-STRENGTH DEPENDENCE OF FORMATION-CONSTANTS .16. PROTONATION OF SOME NITROPHENOLS AND DIHYDROXYBENZOIC ACIDS IN AQUEOUS (TETRAETHYLAMMONIUM IODIDE) SOLUTION AT 25-DEGREES

Citation
A. Derobertis et S. Sammartano, IONIC-STRENGTH DEPENDENCE OF FORMATION-CONSTANTS .16. PROTONATION OF SOME NITROPHENOLS AND DIHYDROXYBENZOIC ACIDS IN AQUEOUS (TETRAETHYLAMMONIUM IODIDE) SOLUTION AT 25-DEGREES, Talanta, 40(5), 1993, pp. 609-614
Citations number
18
Journal title
Talanta
ISSN journal
00399140 → ACNP
Volume
40
Issue
5
Year of publication
1993
Pages
609 - 614
Database
ISI
SICI code
0039-9140(1993)40:5<609:IDOF.P>2.0.ZU;2-D
Abstract
The protonation of 2- and 3-nitrophenol (NO2ph) and 2,X and 3,Y dihydr oxybenzoic acids (DBA, X = 4,5,6; Y = 4,5) has been studied potentiome trically in aqueous tetraethylammonium iodide solutions, at T = 25-deg rees in the ionic strength range 0.05 less-than-or-equal-to I less-tha n-or-equal-to 1M. Besides the species reported in the literature, we h ave also found some dimeric species of 2,4-DBA and 2,5-DBA. Also for t his type of ligand, a simple equation for the dependence on ionic stre ngth of protonation constants, already proposed for several inorganic and organic acids, has been used successfully. Moreover the behavior o f protonation constants as a function of I can give information about the formation of polymeric species.