Abstract

This study focuses on the design of the new dye of donor-π-acceptor (D−π−A) system of methyl 4-((4-aminophenyl)ethynyl)benzoate (MAPEB) to highlight its structural-property relation through a combined experimental and quantum chemical calculation approaches for optical limiting applications. MAPEB was synthesized via aerobic condition palladium-catalysed Sonogashira cross-coupling reaction with good yield. This molecular structure was confirmed by single crystal X-ray crystallographic analysis and the crystal exhibits monoclinic non-centrosymmetric space group of Pc. The existence of intermolecular interactions was confirmed by Hirshfeld analysis, showing high contribution of C⋯H contact which suggested the high nonlinear optical response of the compound. The experimental spectroscopic data including Fourier Transform Infrared (FT-IR), 1H and 13C Nuclear Magnetic Resonance, electronic absorption spectra, HOMO-LUMO energy gap were compared with Density Functional Theory (DFT) at 6–311++G (d,p) basis set. The experimental results complement the theoretical findings in supporting anticipated electronic properties of the molecule. Additionally, the z-scan analysis unveils an excellent value of χ3 of MAPEB in the order of 10−6 esu which indicate good nonlinear optical material under 532 nm continuous wave laser. Low optical limiting action was measured at 110 kW/cm2 which is suitable for various continuous wave laser applications. These findings prove that MAPEB has the potential to be employed as NLO materials for photonic applications.

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