Experimental methods employed oligopyrrin traps to create new B III subporphyrins, indicating potential in coordination chemistry.
Installations of oligopyrrin‐straps at meso ‐bromo and B‐(3‐bromophenyl) B III subporphyrin were attempted by Pd‐catalyzed coupling reactions with α , α ’‐diborylated oligopyrins. While the reaction with a α , α ’‐diborylated dipyrrin gave a 2:2 macrocycle, those with α , α ’‐diborylated tripyrrin and BF 2 ‐complexed tetrapyrrin gave tripyrrin‐ and BF 2 ‐complexed tetrapyrrin‐strapped B III subporphyrins, respectively, as the first example bearing a strap across the meso ‐ and axial‐aryl‐positions of B III subporphyrin. The tripyrrin‐strapped subporphyrin was shown to possess a Pd II coordinating ability.
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Xiao et al. (2025) studied this question.
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