posted on 2022-02-16, 18:16authored byBhupendra
P. Mali, Soumya Ranjan Dash, Anupam Biswas, Kumar Vanka, Kochunnoonny Manoj, Rajesh G. Gonnade
Polymorphs
of fluorescent organic materials offer significant implications
in optoelectronics and advanced materials as they modulate photoluminescence
properties. A slight alteration in the conformation/packing of molecules
in the crystals shows variation in photoluminescence. This necessitates
the polymorph screening of these materials to develop novel crystalline
forms with distinct fluorescence emissions for broader application.
In continuation of our work on the polymorph screening of Green Fluorescence
Protein Chromophore (GFPc), we have synthesized a new imidazoline
derivative, ethyl (Z)-2-(2-methyl-5-oxo-4-(3,4,5-trimethoxybenzylidene)-4,5-dihydro-1H-imidazol-1-yl)acetate (1). Polymorph screening
of 1 under different crystallization conditions revealed
three polymorphs, Form I (needle), Form II (block), and Form III (polycrystalline
material). Forms I and II are the outcome of solution crystallization,
whereas Form III was produced from the melt crystallization of Forms
I and II. DSC, HSM, and powder and single-crystal XRD studies indicate
the conversion of Form I and Form III crystals to Form II crystals
on thermal stimuli. The photoluminescence studies revealed cyan, yellow,
and yellowish-green fluorescence emission for Forms I, II, and III
crystals, respectively. The difference in photoluminescence could
be due to the variance in aggregation modes like H-aggregation in Form I and J-aggregation in Form
II crystals. Form I, Form II, and Form III crystals also showed irreversible
thermal fluorescent switching from cyan-yellow-green due to polymorphic
phase transitions. The study correlates the direct observation of
the modulation of the excited-state transition under thermal stimuli
in the crystalline phase. It will help augment the pace in the research
of thermally responsive fluorescent materials.