Effects of donor and acceptor substituents on the photophysics of 4-ethynyl-2,1,3-benzothiadiazole derivatives

The present work explores the photophysical, electrochemical, and fluorescence polarization properties of a group of pi-conjugated phenylethynyl-2,1,3-benzothiadiazole derivatives (BTDs) bearing different electron-donating (ED) or electron-withdrawing (EW) substituents at the para position of the phenylethynyl moiety. The BTDs were synthesized through the Sonogashira cross-coupling reaction between 4-bromo-2,1,3-benzothiadiazole and the respective para-substituted phenylethynyl derivatives. The BTDs with the EW-substituents show relatively weak solvatochromic behavior, while the BTDs with the strong ED-substituents like methoxy and N,N-dimethylamino-based substituents (BTDPhOMe and BTDPhNMe2) exhibit a pronounced solvatochromic behavior. The change in dipole moments in the excited states of the derivatives was calculated using Lippert-Mataga plots. The conclusions drawn on the spectral behavior of the molecules could be rationalized by TD-DFT calculations involving electron density difference (EDD) maps that correlate with the ICT characteristics of the molecules. The experimental and theoretical calculations reveal that the BTDs with the strong ED-substituents (strong push-pull type BTDs) have a strong ICT character in the excited state. These strong push-pull type BTDs show high fluorescence quantum yield (phi F) in apolar solvents and low phi F in polar solvents. In contrast, the BTDs with the weak ED-substituents (weak push-pull type BTDs) and EW-substituents (pull-pull type BTDs) have a weaker ICT character with low phi F in apolar and high phi F in polar solvent media. There is good a agreement among the HOMO-LUMO band gaps obtained from absorption spectroscopy and electrochemical studies and theoretical calculations. The fluorescence anisotropy measurement in the glycerol medium shows that the studied BTDs generally exhibit higher sensitivity towards microviscosity than the traditional DPH fluorescence anisotropy probe. Photophysical and fluorescence polarization properties of a set of pull-pull and push-pull type pi-conjugated phenylethynyl-2,1,3-benzothiadiazole derivatives.

Automated summary

This study explores the photophysical, electrochemical, and fluorescence polarization properties of a group of pi-conjugated phenylethynyl-2,1,3-benzothiadiazole derivatives. It is found that derivatives with strong electron-donating substituents exhibit pronounced solvatochromic behavior and a strong ICT character in the excited state. Different types of BTDs show different fluorescence quantum yields in different solvent media.