Synthesis and analytical applications of 4-aminopyrazolone derivatives as chromogenic agents for the spectrophotometric determination of phenols

Citation
Yc. Fiamegos et al., Synthesis and analytical applications of 4-aminopyrazolone derivatives as chromogenic agents for the spectrophotometric determination of phenols, ANALYT CHIM, 403(1-2), 2000, pp. 315-323
Citations number
23
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
ANALYTICA CHIMICA ACTA
ISSN journal
00032670 → ACNP
Volume
403
Issue
1-2
Year of publication
2000
Pages
315 - 323
Database
ISI
SICI code
0003-2670(20000103)403:1-2<315:SAAAO4>2.0.ZU;2-N
Abstract
The synthesis of simple, extensively conjugated chromophores as substitutes for 4-aminoantipyrine (4-AAP) capable of causing hyperchromic shifts when coupled with phenols is described. The 4-aminopyrazolone derivatives synthe sised are subsequently applied for the spectrophotometric assay of phenolic compounds and the advantages of each of the proposed systems are highlight ed. No improvement is made on the detection of para-substituted phenols as well as polychlorophenols (e.g. pentachlorophenol). An increase in the sens itivity of coupling products is obtained for certain phenolic compounds as indicated from the comparison of the individual responses. The proposed met hods have analogous analytical features and in some cases show considerable improvements compared to the 4-AAP method. Beer's law is obeyed over a wid e dynamic range (up to ca. 500 mu g/l) and the relative standard deviations are <3.4%. The methods are applied satisfactorily for phenol assay in real samples, however, taking into account the intrinsic differences of the met hods in the responses to the various phenolic compounds. (C) 2000 Elsevier Science B.V. All rights reserved.