Synthesis of Cationic Azatriphenylene Derivatives by Electrochemical Intramolecular Pyridination and Characterization of Their Optoelectronic Properties.
Yushi OhnoShogo AndoDaisuke FurushoRyoyu HifumiYuuya NagataIkuyoshi TomitaShinsuke InagiPublished in: Organic letters (2023)
Here, a facile and selective synthesis method for cationic azatriphenylene derivatives was established by electrochemical intramolecular cyclization, where atom-economical C-H pyridination without a transition-metal catalyst or an oxidant is a key step. The proposed protocol is a practical strategy for the late-stage introduction of cationic nitrogen ( N + ) into π-electron systems and broadens the scope of molecular design of N + -doped polycyclic aromatic hydrocarbons.
Keyphrases
- polycyclic aromatic hydrocarbons
- transition metal
- ionic liquid
- highly efficient
- gold nanoparticles
- quantum dots
- metal organic framework
- electron transfer
- visible light
- reduced graphene oxide
- energy transfer
- molecularly imprinted
- randomized controlled trial
- label free
- structure activity relationship
- high resolution
- carbon dioxide
- mass spectrometry