Elucidating the Structure-Nonlinear Optical Property Relationship of Ethynyl Extended Benzanthrone Chromophores

Three ethynyl-extended benzanthrone derivatives with benzonitrile (Dye A), thiophene (Dye B), and methyl propiolate (Dye C) as substituents were synthesized and investigated to illustrate structure-property relationships governing their nonlinear optical (NLO) behavior. The third-order nonlinear absorption and refractive index of three dyes were studied using open- and closed-aperture z-scan measurements under 532 nm continuous-wave laser excitation. All dyes exhibited reverse saturable absorption dominated by two-photon absorption, with Dye A showing the highest nonlinear absorption coefficient (βeff = 2.3 × 10^-5 cm/W) and two-photon response, attributed to its extended conjugation and smaller HOMO-LUMO gap (6.45 eV). Closed-aperture Z-scans revealed strong nonlinear refraction (n₂), with the thiophene-substituted Dye B displaying the largest n₂ (14.8 × 10^-9 cm²/W) and third-order susceptibility (χ³ = 3.1 × 10^-6 esu). The evaluated optical switching figures of merit met the requirements for all-optical switching and optical limiting. DFT and TDDFT calculations demonstrated that donor substitution and conjugation length govern electronic structure, charge transfer character, and global reactivity descriptors. Enhanced electronic softness and hyperpolarizability in Dye B further support its superior refractive nonlinearity. These results establish clear structure-property correlations and highlight donor engineering as an effective strategy for developing organic nonlinear optical and photonic materials.