Investigation of Pyrene vs. Anthracene-based Oxime Esters: Role of the Excited States on Their Polymerization Initiating Abilities

International audienceIn this work, two series of oxime esters (OXE) based on Pyrene and Anthracene chromophores were synthesized and tested as Type Ⅰ photoinitiators for the Free Radical Photopolymerization (FRP) under visible irradiation at 405 nm using light-emitting diodes (LED) as the irradiation source. Interestingly, the two series of oxime esters only differ by the nature of the substituents connected to the oxime ester functional group. As a result of this modification, the reactivity of the different compounds only depends on the rate of decomposition from their excited states as well as the reactivity of the generated radicals. Remarkably, the 18 Pyrene-based OXEs (Py-OXE) and 17 Anthracene-based OXEs (An-OXE) were never synthesized prior to this work. Pyrene and Anthracene chromophores were selected as benchmark structures reacting mainly from their first excited singlet (S1) and triplet (T1) states, respectively. This will allow to shed some light on the excited states responsible of the cleavage of OXEs. Therefore, originality of this study relies in the difference of the initiation ability between these two families. In fact, the results showed that Py-OXEs (0.5% w) are the most efficient systems compared to An-OXEs, so that higher final conversions and rates of polymerization could be obtained with Py-OXEs. Influence of the OXE structure (both chromophores and leaving groups) is discussed on the basis of different characterization techniques such as: UV-visible absorption spectroscopy, photolysis experiments, real-time Fourier transform infrared spectroscopy (RT-FTIR), stationary fluorescence and time-2 resolved fluorescence. Therefore, a global mechanism is finally provided based on the complementary characterization data. Oxime ester derivatives were also tested under air for the generation of 3D patterns (by Direct Laser Write DLW) using a diode laser at 405 nm