N-Bridge Head Indolizin (Benzindolizin)-ium Iodide as Privileged Precursor in Heterocyclic Cyanine Dye Synthesis

A. I. M. Koraiem ^[2] | M. M. Gommaa ^[2] | H. A. El-Damarany ^[2] | M. H. Yosry ^[2]

Abstract: 3-Methyl-1-phenyl-pyrazolin-5-imin-4 (2)-indolizine (benzoindolizine)-zero-3 (4)-methine (27).3-methyl-1-phenyl-pyrazolin-5-imine-4 (2)-indolizine (benzo- indolizine)-B-substituted di-1- [2 (4)] methine cyanine dyes (28a-d).3-methyl-1-phenyl-pyrazolin-5-imine-4 (2)-indolizine (benzo indolizine)-? (?) disubstituted- bis-di- [2 (4)] methine cyanine dyes (30a-f) were synthesised based on 4-acetyl-1, 5-dimethyl-3-phenyl-3, 4-di [H] pyrazolo [4', 3':5, 6] pyrido [4, 3-b] indolizin-6-ium iodide & 4-Acetyl-1, 5-dimethyl-3-phenyl-3, 4-di [H] Pyrazolo [4', 3':5, 6] pyrido [4, 3-b] indolizin-6-ium-iodide (26a, b) & 1, 5-dimethyl-3-phenyl-3, 4-di [H] pyrazolo [4', 3':5, 6] pyrido [4, 3-b] indolizin-6-ium-iodide-4-?-substituted-?, ?-unsaturated carbonyl derivatives (29a-f). The new synthesized cyanine dyes were identified by elemental & spectral analyses. The UV-visible absorption spectra of some selected dyes were investigated in pure organic solvents and in aqueous universal buffer solutions.

Keywords: Indolizine, Benzindolizine, Cyanine Dye Synthesis, Solvato-(Media)-chromic Behaviour

Edition: Volume 9 Issue 8, August 2020,

Pages: 795 - 803