72695-32-0Relevant articles and documents
Bis(2-nitrophenyl) selenide, bis(2-aminophenyl) selenide and bis(2-aminophenyl) telluride: Structural and theoretical analysis
Butcher, Ray J.,Saravanan, Raju,Singh, Harkesh B.
, p. 271 - 280 (2021/06/14)
Three organoselenium and organotellurium compounds containing ortho substitutents, namely, bis(2-nitrophenyl) selenide, C12H8N2O4Se, 2, bis(2-aminophenyl) selenide, C12H12N2Se, 3, and bis(2-aminophenyl) telluride, C12H12N2Te, 7, have been investigated by
Walking Down the Chalcogenic Group of the Periodic Table: From Singlet to Triplet Organic Emitters
Kremer, Adrian,Aurisicchio, Claudia,Deleo, Federica,Ventura, Barbara,Wouters, Johan,Armaroli, Nicola,Barbieri, Andrea,Bonifazi, Davide
supporting information, p. 15377 - 15387 (2015/11/02)
The synthesis, X-ray crystal structures, ground- and excited-state UV/Vis absorption spectra, and luminescence properties of chalcogen-doped organic emitters equipped on both extremities with benzoxa-, benzothia-, benzoselena- and benzotellurazole (1
Microwave-assisted one-pot synthesis of symmetrical diselenides, ditellurides and disulfides from organoyl iodides and elemental chalcogen catalyzed by CuO nanoparticles
Botteselle, Giancarlo V.,Godoi, Marcelo,Galetto, Fabio Z.,Bettanin, Luana,Singh, Devender,Rodrigues, Oscar E.D.,Braga, Antonio L.
, p. 186 - 193 (2013/01/14)
In this study CuO nanoparticles were applied as a catalyst for CSe, CTe, and CS bond formation. The reaction was performed with organoyl iodides and elemental selenium, tellurium or sulfur under microwave irradiation in the presence of a base and solvent at 80 °C. This novel protocol allowed the synthesis of a variety of diselenides, ditellurides and disulfides in good to excellent yields in a very short reaction time.