Abstract:In this study, two novel single-component photoinitiators (PIs) based on thioxanthone derivatives, named CLT1 and CLT2, were synthesized by covalently linking thioxanthone framework with hydrogen-donors 1,2-dimethoxybenzene and 2,3-dihydrobenzo[b][1,4]dioxine through a chalcone structure. The performance of these PIs was comprehensively evaluated using variety of methods including UV-visible absorption spectroscopy, fluorescence emission spectroscopy, steady-state photodegradation tests, thermal stability tests, and photopolymerization kinetic tests. These results indicate that the novel PIs CLT1 and CLT2 possess not only excellent UV-visible light absorption capabilities but also outstanding thermal stability and photopolymerization initiated efficiency. Particularly, CLT1 and CLT2 exhibited double-bond conversion rates exceeding 90% in the polymerization of the monomer TPGDA at various concentrations, higher than that of the commercial ITX system, exhibiting potential value in practical application.