Issue 48, 2015

Synthesis and photophysics of selective functionalized π-conjugated, blue light emitting, highly fluorescent C7-imidazo indolizine derivatives

Abstract

A new family of novel highly fluorescent π-conjugated, C7-imidazole based indolizine derivatives has been prepared in good to excellent yields, catalysed by L-proline in acetonitrile. These are π-conjugated, C7-imidazole based indolizine derivatives covering the emission wavelength range 423–449 nm in acetonitrile with high quantum yields at 25 °C. A thorough photophysical study of all the compounds has been carried out to understand the π-conjugated electronic effect of the imidazole moiety fused at the C7 position on the indolizine motif. In addition, a comparative photophysical study of three selective fluorophores was also carried out in a wide variety of solvents at 25 °C. Finally, the molecular orbitals of the two representative compounds were investigated through DFT calculations to illustrate the pi-conjugate effect.

Graphical abstract: Synthesis and photophysics of selective functionalized π-conjugated, blue light emitting, highly fluorescent C7-imidazo indolizine derivatives

Supplementary files

Article information

Article type
Paper
Submitted
06 Aug 2015
Accepted
09 Oct 2015
First published
09 Oct 2015

Org. Biomol. Chem., 2015,13, 11674-11686

Synthesis and photophysics of selective functionalized π-conjugated, blue light emitting, highly fluorescent C7-imidazo indolizine derivatives

R. Sarkar, T. Chaudhuri, A. Karmakar and C. Mukhopadhyay, Org. Biomol. Chem., 2015, 13, 11674 DOI: 10.1039/C5OB01646K

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