Abstract
High-valent iron halide corroles were examined to determine their reactivity with carbon radicals and their ability to undergo radical rebound-like processes. Beginning with Fe(Cl)(ttppc) (1) (ttppc = 5,10,15-tris(2,4,6-triphenylphenyl)corrolato(3-)), the new iron corroles Fe(OTf)(ttppc) (2), Fe(OTf)(ttppc)(AgOTf) (3), and Fe(F)(ttppc) (4) were synthesized. Complexes 3 and 4 are the first iron triflate and iron fluoride corroles to be structurally characterized by single crystal X-ray diffraction. The structure of 3 reveals an Ag(I)-pyrrole (η(2)-π) interaction. The Fe(Cl)(ttppc) and Fe(F)(ttppc) complexes undergo halogen transfer to triarylmethyl radicals, and kinetic analysis of the reaction between (p-OMe-C(6)H(4))(3)C• and 1 gave k = 1.34(3) × 10(3) M(-1) s(-1) at 23 °C and 2.2(2) M(-1) s(-1) at -60 °C, ΔH(⧧) = +9.8(3) kcal mol(-1), and ΔS(⧧) = -14(1) cal mol(-1) K(-1) through an Eyring analysis. Complex 4 is significantly more reactive, giving k = 1.16(6) × 10(5) M(-1) s(-1) at 23 °C. The data point to a concerted mechanism and show the trend X = F(-) > Cl(-) > OH(-) for Fe(X)(ttppc). This study provides mechanistic insights into halogen rebound for an iron porphyrinoid complex.