1379868-89-9Relevant academic research and scientific papers
From thia- to selenadiazoles: Changing interaction priority
Lindner, Benjamin D.,Coombs, Benjamin A.,Schaffroth, Manuel,Engelhart, Jens U.,Tverskoy, Olena,Rominger, Frank,Hamburger, Manuel,Bunz, Uwe H. F.
, p. 666 - 669 (2013)
The synthesis, optical, and electrochemical properties as well as solid-state structures of a series of alkynylated, benzannulated selenadiazoles are reported. This set of compounds is compared to the lighter homologue series, the thiadiazoles. The selena
Hexaazatrinaphthylenes with different twists
Choudhary, Sunil,Gozalvez, Cristian,Higelin, Alexander,Krossing, Ingo,Melle-Franco, Manuel,Mateo-Alonso, Aurelio
supporting information, p. 1525 - 1528 (2014/03/21)
A synthetic strategy that allows the induction of twist angles of different sizes in 5,6,11,12,17,18-hexaazatrinaphthylene (HATNA) chromophores is reported. The different twist angles are accompanied by measurable changes in the emission and electrochemic
Synthesis and optical properties of diaza- and tetraazatetracenes
Lindner, Benjamin D.,Engelhart, Jens U.,Maerken, Michaela,Tverskoy, Olena,Appleton, Anthony L.,Rominger, Frank,Hardcastle, Kenneth I.,Enders, Markus,Bunz, Uwe H. F.
supporting information; experimental part, p. 4627 - 4633 (2012/05/04)
A series of functionalized diaza- and tetraazatetracenes was synthesized, either by condensation of an aromatic diamine with an ortho-quinone/ diethyloxalate followed by chlorination with POCl3 to give diazatetracenes or by palladium-catalyzed
