Abstract 2,3′-Azacorrole dimer was synthesized via regioselective oxidative coupling of 10-azacorrole by p-chloranil in the presence of trifluoroacetic acid in moderate yield. The structures of all the products were characterized thoroughly by NMR and HRMS. The UV-Vis absorption spectra show obvious bathochromic shifts of both the Soret band and Q bands, along with a marked increase in the absorbance of the Q bands.
No takes yet. Share an insight, caveat, or question.
Chen et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: