Photophysical, kinetic and thermodynamic study of one-component Type II thioxanthone acetic acid photoinitiators


Metin E., ARSU N. , Catak S., Aviyente V.

EUROPEAN POLYMER JOURNAL, cilt.136, 2020 (SCI İndekslerine Giren Dergi) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 136
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1016/j.eurpolymj.2020.109909
  • Dergi Adı: EUROPEAN POLYMER JOURNAL

Özet

In this study, One-Component Type II thioxanthone acetic acid based photoinitiators, as well as the conventional Type II photoinitiator with phenyl acetic acid based co-initiators, have been investigated in terms of their photophysical, kinetic and thermodynamic properties by a series of Density Functional Theory (DFT) calculations. Experimental UV-Vis spectra have been compared with computationally generated UV-Vis spectra via Time-Dependent DFT (TD-DFT) and by taking into consideration the vibrational and dynamic effects (Wiggler). Natural transition orbitals have been generated for thioxanthone acetic acid derivatives to understand the physical nature of electronic transitions. Furthermore, kinetic and thermodynamic parameters of radical attack to the monomer of thioxanthone acetic acid based radicals and phenyl acetic acid based co-initiator radicals have been investigated. Comparison of the thermodynamic parameters of the initiating radicals has shown that initiation is more favorable with exocyclic radicals in both cases. Exocyclic radicals of the thioxanthone acetic acid derivatives and phenyl acetic acid derivates have been found to have comparable activation energies for their attack to methyl methacrylate. Furthermore, the spin densities and the radical Fukui functions of the attacking radicals have been nicely correlated with the activation barriers. In this way, a fast and predictive approach for the determination of radical reactivity in photopolymerization reactions has been proposed; this enables the evaluation of the initiation efficiency of the photoinitiators prior to synthesis.