Heterocyclic Schiff Bases as Main Entity In Methine&Metal Complexes Cyanine Dyes Synthesis
Journal: International Journal of Science and Research (IJSR) (Vol.9, No. 8)Publication Date: 2020-08-05
Authors : A. I. M. Koraiem; M. M. Gommaa; H. A. El-Damarany; M. H. Yosry;
Page : 773-786
Keywords : Heterocyclic ketomethylene; Schiff Bases iodide salts; cyanine dyes synthesis; spectral; Solvatochromic Behaviour; Acid-Base Properties;
Abstract
Heterocyclic Schiff bases (1a-g) was prepared and employed in the synthesis of substituted ketomethylene acyclic (cyclic) heterocyclic quaternary iodide salts and acyclic pyrazolo and/or cyclic substituted pyrrolo [5, 4-d] pyrazolin-mero-2 (4), pyrrolo [5, 4-d] pyrazolo-zero-3 [4 (1)]methine and pyrrolo [5, 4-d] pyrazolo or pyrazol [4, 5-d] dioxine (thiazine/ oxazine) metal complex cyanine dyes (2a-d, 3A, B, 4a-d& 5a, b, 6A, B& 7a-c, 8a-c, 11a-d, 12, 13a-d, 14a, b& 17). The new synthesized cyanines and their metal chelator complex dyes were identified by elemental& spectral analyses, The absorption spectra and solvatochromic behaviours of the newly selected synthesised dyes was investigated in pure organic solvents, as well as in aqueous universal buffer solutions.
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