Evidence map›Paper›PMID 35637518›Full record

ArticleBMC chemistry2022

Physico-analytical studies on some heterocyclic azo dyes and their metal complexes with some transition metals.

Fathy A El-Seify, Hassan A Azab, Fikrea S Degedy, Khalid A Abdel-Mageed, Farid I El-Dossoki

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Article in BMC chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Fathy A El-SeifyChemistry Department, Faculty of Engineering, Port Said University, Port Said, Egypt.
Hassan A AzabChemistry Department, Faculty of Science, Suez Canal University, Ismalia, Egypt.
Fikrea S DegedyChemistry Department, Faculty of Science, Suez Canal University, Ismalia, Egypt.
Khalid A Abdel-MageedChemistry Department, Faculty of Engineering, Port Said University, Port Said, Egypt.
Farid I El-DossokiChemistry Department, Faculty of Science, Port Said University, Port Said, Egypt. feldossoki64@sci.psu.edu.eg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this investigation, the azo dyes; 2-(3'-phenyl-5'-pyrazolyl azo) schaffer acid (la) and 2-(3'-phenyl-5'-pyrazolyl azo) resorcinol (Ib); were prepared through diazotizing 3-phenyl-5-aminopyrazole (PAP) and coupling the resulting diazonium salt with Schäffer acid and resorcinol respectively. The prepared azo dyes are characterized using both IR spectra and the elemental analysis (C, H, N and S). The prepared azo dyes are used as chromogenic reagents for the spectrophotometric determination of copper (II), nickel (II), cobalt (II) and zinc (II) ions. The conditional acid dissociation constants of these azo dyes (la and Ib) and the stability constants of its metal ion complexes have been determined by spectro-analytical methods. The effect of pH, time, organic solvent and the foreign ions on the spectrophotometric determination of these ions and their complexes with the azo dyes under study were studied. The stoichiometric ratio (M:L) of the formed complexes was also determined. The molar absorptivity, the Sandell's sensitivity values, the obeyance of Beers law and the stability constants of the formed complexes have been also determined and discussed.

Indexed as

Azo dyeChromogenic reagentsHeteroaromatic aminesSpectrophotometric

Identifiers

PMID35637518
PMCPMC9153159

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