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1,3,5-Triaryl-1,3,5-Triazinane-2,4,6-Trithiones: Synthesis, Electronic Structure and Linear Optical Properties.

Ismaël RabouelNicolas RichyAnissa AmarAbdou BoucekkineThierry RoisnelOlivier MonginMark G HumphreyFrédéric Paul
Published in: Molecules (Basel, Switzerland) (2020)
The 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.
Keyphrases
  • molecular docking
  • density functional theory
  • molecular dynamics simulations
  • energy transfer
  • molecular dynamics
  • structure activity relationship
  • single molecule
  • neural network
  • monte carlo