Electronic spectra, solvatochromic behaviour, and acidity constants of some new azocoumarin derivatives

Citation
Nm. Rageh et al., Electronic spectra, solvatochromic behaviour, and acidity constants of some new azocoumarin derivatives, CHEM PAP-CH, 53(2), 1999, pp. 107-113
Citations number
17
Categorie Soggetti
Chemistry
Journal title
CHEMICAL PAPERS-CHEMICKE ZVESTI
ISSN journal
03666352 → ACNP
Volume
53
Issue
2
Year of publication
1999
Pages
107 - 113
Database
ISI
SICI code
0366-6352(1999)53:2<107:ESSBAA>2.0.ZU;2-#
Abstract
The UV visible electronic spectra of some azocoumarin dyes derived from 6-a minocoumarin have been studied. The different bands observed have been assi gned to the proper electronic transitions. The compounds exist mainly in th e azo form but some of them exhibit an azo reversible arrow hydrazone tauto meric equilibrium. Solvatochromic behaviour of these compounds was investig ated by studying their visible spectra in pure and mixed organic solvents o f different characters. The longest wavelength band displayed by the azocou marin derivatives in DMF solution is assigned to an intermolecular CT trans ition. The solvated H-bonding complexes formed between DMF and 8-hydroxyqui noline derivatives were investigated. Delta G and K-f values of these compl exes have been determined. The acidity constants of six compounds were dete rmined from the spectra in aqueous-ethanolic solutions of varying pH values .