Abstract
Purpose - The purpose of this study aims to synthesize a novel donor-acceptor dye based on phenothiazine as a donor (D) and nonconjugated spacer was devised and synthesized by condensing of 2,2'-(1H-indene-1,3(2H)-diylidene) dimalononitrile with aldehyde and the practical synthesis methodology as given in Scheme 1. Design/methodology/approach - The prepared phenothiazine dye was systematically experimentally and theoretically examined and characterized using nuclear magnetic resonance spectroscopy (1H,13C NMR), Fourier-transform infrared spectroscopy (IR) and high-resolution mass spectrometry. Density functional theory (DFT) and time-dependent density functional theory DT-DFT calculations were implemented to determine the electronic properties of the new dye Findings - The UV-Vis absorption and fluorescence spectroscopy of the synthesized dye was investigated in a variety of solvents with varying polarities to demonstrate positive solvatochromism correlated with intramolecular charge transfer (ICT). The probe's quantum yields (CYRILLIC CAPITAL LETTER EFf) are experimentally measured in ethanol, and the Stokes shifts are found to be in the 4846-9430 cm(-1) range. Originality/value - The findings depicted that the novel (D-pi-A) chromophores may act as a significant factor in the organic optoelectronics.