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Synthesis, characterization and solvatochromic behaviour of new water-soluble 8-hydroxy-3,6-disulphonaphthyl azohydroxynaphthalenes

A series of five tetracyclic mono azo dyes based on the diazotization of 1-amino-8-hydroxynaphthalene-3,6-disulphonic acid and subsequent coupling with substituted (un)sulphonated naphthalene derivatives have been synthesized. The chemical structures of the dyes were established using UV–visible, IR...

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Published: 2022
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LEADER 00000njm a2000000a 4500
001 oai:repository.ui.edu.ng:123456789/12100
042 |a dc 
720 |a Thomas O.E.  |e author 
720 |a Adegoke, O.A.  |e author 
260 |c 2022 
520 |a A series of five tetracyclic mono azo dyes based on the diazotization of 1-amino-8-hydroxynaphthalene-3,6-disulphonic acid and subsequent coupling with substituted (un)sulphonated naphthalene derivatives have been synthesized. The chemical structures of the dyes were established using UV–visible, IR, NMR as well as mass spectrometry. Based on the number of sulphonic acid and other hydrophilic groups they contain, the compounds showed varying extent of water solubility. Spectroscopic characterization revealed the existence of azohydrazone tautomerism and the influence of the structures of solvating solvents on the equilibrium. Statistical analysis of single, dual and multiparametric equations of Kamlet Abboud and Taft parameters showed that solvent polarity was the most significant contributor to the observed spectral patterns of the dyes in pure solvents. The compounds could find useful applications as solvatochromic probes, food and drug colour additives. 
024 8 |a 1658-3655 
024 8 |a ui_art_thomas_synthesis_2022 
024 8 |a Journal of Taibah University for Science 16(1), pp. 451-462 
024 8 |a https://repository.ui.edu.ng/handle/123456789/12100 
653 |a 1-amino-8-hydroxynaphthalene-3 6-disulphonic acid 
653 |a azo compounds 
653 |a synthesis 
653 |a spectroscopic characterization 
653 |a azo-hydrazone tautomerism 
653 |a solvatochromic properties 
245 0 0 |a Synthesis, characterization and solvatochromic behaviour of new water-soluble 8-hydroxy-3,6-disulphonaphthyl azohydroxynaphthalenes