Synthesis and Photophysical, Electrochemical, and DFT Studies of Piperidyl and Pyrrolidinyl Chalcones
Humera Baig, Amber Iqbal, Alvina Rasool, Syed Zajif Hussain, Javed Iqbal, Meshari Alazmi, Nawaf Alshammari, Amira Alazmi, Amer AlGhadhban, Abdel Moneim Elhadi Sulieman, Kamaleldin B. Said, Habib ur Rehman, Rahman Shah Zaib Saleem
Abstract
High Resolution Image Download MS PowerPoint Slide Small organic molecules with interesting optical and electrochemical properties find applications as organic luminescent materials. In this work, we report the synthesis of novel chalcones with D–A–D and D–A–D–A architecture, followed by their optical, electrochemical, and computational studies. The absorption band of these compounds occurs at 360–480 nm with emission maxima appearing around 513–552 nm. The large Stokes shifts (Δλ) for all compounds (90–132 nm) suggest intramolecular charge transfer (ICT) in the excited states. The molar absorptivity and fluorescence quantum yields were found to be in the range of 1.7–4.26 × 10 4 M –1 cm –1 and 0.29–0.39, respectively. The electrochemical parameters were determined by using cyclic voltammetry (CV). Density functional theory (DFT) calculations of all compounds were made by using B3LYP/G (d,p) functionals in chloroform and were found to have a good correlation with experimental results. Preliminary studies of absorption, photoluminescence, CV, and their theoretical correlation suggest that these compounds may be optimized for their applications in optoelectronics, sensing, and bioimaging.