Abstract

We report herein an efficient, fast, and sustainable method for the preparation of fluorescent indolizine derivatives under ultrasound (US) irradiation using a one-pot and multicomponent methodology. In solution, the indolizine derivatives present absorption in the UV region and fluorescence emission in the violet-to-blue region with a relatively large Stokes shift. Aggregation-induced enhanced emission (AIEE) was observed in some derivatives by fluorescence studies in water/acetone systems. Regarding this particular property, the substituents showed to play a fundamental role. In the solid state, the derivatives present full-color tunable fluorescence also tailored by the substituents. Theoretical calculations using time-dependent density functional theory were performed to investigate the photophysics of these indolizine derivatives and were able to reproduce with accuracy their more prominent electronic features.

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