Rabouel, IsmaëlRichy, NicolasAmar, AnissaBoucekkine, AbdouRoisnel, ThierryMongin, OlivierHumphrey, MarkPaul, Frederic2022-08-012022-08-011420-3049http://hdl.handle.net/1885/270086The synthesis of four new 1,3,5-triaryl-1,3,5-triazinane-2,4,6-trithione derivatives (thioisocyanurates) and two new partially thionated analogues from the corresponding 1,3,5-triaryl-1,3,5-triazinane-2,4,6-triones (isocyanurates) is reported, together with their spectroscopic properties. DFT calculations and comparison with the corresponding isocyanurates evidence the impact of the oxygen-for-sulfur replacement on the electronic structure and linear optical properties of these heterocycles. A bathochromic shift of the absorption bands and more efficient quenching of the fluorescence was observed.This project was supported by ANR (ANR-17-CE07-0033-01 project).application/pdfen-AU© 2020 by the authors. Licensee MDPI, Basel, Switzerland.http://creativecommons.org/licenses/by/4.0/thioisocyanuratesisocyanuratesthionationDFT calculationscyclic thioureaslinear opticscyclic urea1,3,5-Triaryl-1,3,5-Triazinane-2,4,6-Trithiones: Synthesis, Electronic Structure and Linear Optical Properties202010.3390/molecules252254752021-08-01Creative Commons Attribution (CC BY) license