Abstract
Given the pivotal role of coumarins as tunable nonlinear optical (NLO) materials for advanced photonics, this study aims to decipher the regulatory mechanisms governing their excited-state dynamics and nonlinear absorption. In this study, two amino-coumarin dyes (102 and 153) differing in electron-withdrawing groups are synthesized to probe the impact of intramolecular charge transfer (ICT) on transient dynamics and nonlinear absorption. Frontier orbital and natural transition orbital analyses reveal subtle alterations in the ICT characteristics of amino-coumarin molecules. These minor modifications induce a significant red shift in the stimulated emission band within transient absorption spectroscopy, ultimately triggering a transition from reverse saturable absorption (RSA) to saturable absorption (SA) at 515 nm. Our findings demonstrate that, with straightforward molecular modifications, coumarins emerge as promising dual-function materials for saturable absorption and optical limiting.