Abstract
The formation of octahedral tris(5-phenyl-4,6-dipyrrinato) complexes of cobalt(III) and iron(III) of p-subsituted (−H, −CO 2Me, −NO 2) 5-phenyl-4,6-dipyrrins is described. The molecular structure of the parent cobalt(III) complex was determined by X-ray crystallography. Crystals of C 45H 33N 6Co·C 3H 6O are monoclinic, a = 13.539(2), b = 22.348(2), c = 13.467(1) A ̊ , V = 3882.7(8) A ̊ 3, Z = 4 , space group C2/ c. The structure was solved by direct methods and refined by full-matrix least-squares procedures to R = 0.039 and Rw = 0.033 for 2309 reflections with 1 ≥ 3 σ ( F 2). These regular octahedral complexes underline the special coordination properties of the 5-phenyl-4,6-dipyrrins as compared to α,β-alkyl-substituted dipyrrins for which no such tris-complexes are known. The reduction of the p-nitro-substituted Co(III) complex to the corresponding p-amino complex and the saponification, chlorination and esterification of the p-methoxycarbonyl-substituted Co(III) complex are reported, highlighting the chemical stability of the complexes and their potential to be incorporated into larger structures.
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