4.6 Article

Synthesis, spectroscopic properties, and DFT correlative studies of 3,3′-carbonyl biscoumarin derivatives

Journal

JOURNAL OF MOLECULAR STRUCTURE
Volume 1243, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molstruc.2021.130781

Keywords

Carbonyl biscoumarin; Dipole moments; HOMO-LUMO; Solvatochromism; Chemical hardness

Funding

  1. department of science and technology, ministry of science and Technology, India

Ask authors/readers for more resources

A facile method for synthesizing a library of 3,3'-Carbonyl biscoumarin derivatives via one-pot chemical reaction was reported, with the synthesized fluorescent dyes being purified and characterized. The study investigated the solvatochromic behavior and dipole moments of the fluorescent dyes in different solvents, showing a redshift in absorption spectra with increased solvent polarity. Results indicated the potential application of these fluorescent dyes as probes and in the construction of dye-sensitized solar cells.
A facile and simple method for the synthesis of a library of 3,3'-Carbonyl biscoumarin derivatives via a one-pot chemical reaction is reported. The synthesized fluorescent dyes were purified and characterized by analytical methods. The IR, 1H-NMR, and MS results confirmed the corresponding structure of the fluorescent dyes. The absorption and fluorescence spectra of fluorescent dyes were recorded in different solvents of varying polarity to understand the solvatochromic behaviour and dipole moments. Stoke's shift exhibits a redshift with an increase in solvent polarity for all molecules indicating a pi ->pi* transition. The ground state dipole moments of all fluorescent dyes are estimated theoretically from ab initio computations (integral equation formalism of polarizable continuum model) and experimentally from the solvatochromic method and the results are compared. Further, using solvatochromic correlations like Lippert's, Bakhshiev's, Kawski-Chamma-Viallet's, and solvent polarity parameter the excited state dipole moments are determined. Results show that the excited state dipole moments are higher than the ground state dipole moments which suggests that, all fluorescent dyes are more polar in the excited state. The HOMOLUMO energy gaps computed from density functional theory and absorption threshold wavelengths are found to be in good agreement and also support intramolecular charge transfer (ICT). Using HOMO-LUMO energies, the chemical hardness (eta) of the molecules is determined and the chemical stability is discussed. Further, using DFT molecular electrostatic potential (MESP) plots, the electrophilic site and nucleophilic site which are useful in photochemical reactions were identified. The preliminary observations and results suggest that the fluorescent dyes can be considered as potential candidates for fluorescent probes and construction of dye-sensitized solar cell in future (C) 2021 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available