Abstract

AbstractGiven the increased interest in phosphorus corroles for many applications, we now report how their photophysical variables and redox potentials may be tuned. This was performed by focusing on a series of derivatives that significantly differ in terms of the chelating corrole macrocycle: three C6F5vs. three CF3substituents on themeso‐C atoms, Hvs. Br atoms on the β‐pyrrole positions, and monomericvs. dimeric (throughβ‐pyrrole C−C bonds). Also studied was the effect of the phosphorus axial ligands, hydroxidevs. fluoride.

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