1419263-36-7

Upstream product

• 1419263-34-5 2,6,10-tri-tert-butyl-4,8-bis(dicyanomethylidene)-4H,8H-dibenzo[cd,mn]pyren-12-ol 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant academic research and scientific papers

An extremely redox-active air-stable neutral π radical: Dicyanomethylene-substituted triangulene with a threefold symmetry

Radically active: A redox-active air-stable neutral π radical (1 .) with three dicyanomethylene groups introduced with threefold symmetry into a triangulene ?? skeleton instead of the oxygen atoms of TOT. was designed, synthesized, and characterized (see figure). The enhanced electron-accepting ability and extended π-electronic system of this chemical modification gave an extremely small SOMO-LUMO gap and significantly lowered the frontier orbital energies, leading to the remarkable increase in the redox stages.