863191-40-6Relevant academic research and scientific papers
3,5,7,9-tetraphenylhexaazaacridine: A highly stable, weakly antiaromatic species with 16 π electrons
Langer, Peter,Bodtke, Anja,Saleh, Nehad N. R.,Goerls, Helmar,Schreiner, Peter R.
, p. 5255 - 5259 (2005)
(Chemical Equation Presented) Zwitterionic structures with very low lying triplet states are the dominant characteristics of the first hexaazaacridine, 3,5,7,9-tetraphenylhexaazaacridine (TPH-acridine, see picture), and the analogous TPH-anthracene. The s
3,5,7,9-Substituted hexaazaacridines: Toward structures with nearly degenerate singlet-triplet energy separations
Langer, Peter,Amiri, Shadi,Bodtke, Anja,Saleh, Nehad N. R.,Weisz, Klaus,Goerls, Helmar,Schreiner, Peter R.
, p. 5048 - 5063 (2008/12/20)
(Chemical Equation Presented) Toward the goal of preparing stable, neutral open-shell systems, we synthesized a novel series of p-phenyl-substituted 3,5,7,9-hexaazaacridine and 3,5,7,9-hexaazaanthracene derivatives. The effects of substitution on the mole
