Crystal structures of metalloporphyrin complexes. Effects of Fe(III)-halide bond lengths and intermolecular interactions on crystal packing

The structures of four Fe(III) complexes dedicated to the memory of Prof. A. B. P. Lever (Barry), which involve porphyrin halides Fe(TPP)X (where TPP[Formula: see text] meso-tetraphenylporphyrinate; X [Formula: see text] F, Fe–F; Cl, Fe–Cl; Br, Fe–Br; I, Fe–I), at 100(2) K, as well as Fe–F at 143(2) K, have been determined through single-crystal X-ray diffraction. In solution, all four compounds exhibit [Formula: see text] symmetry; however, they form different crystal structures mainly due to variations in Fe–X bond lengths and intermolecular interactions. Crystals of Fe–F and Fe–Cl belong to the tetragonal [Formula: see text]4/[Formula: see text] (No. 87) and [Formula: see text]4 (No. 79) space groups, respectively, maintaining the [Formula: see text] axis through the Fe–X bonds. Both Fe–Br and Fe–I adopt the monoclinic [Formula: see text]2 1 /[Formula: see text] (No. 14) space group with unique features. The shortest Fe–Fe distances are 9.6782 Å in Fe–F ([Formula: see text]4/[Formula: see text], 9.7086 Å in Fe–Cl ([Formula: see text]4), and 8.943 Å and 9.019 Å in Fe–Br and Fe–I, respectively. Hirshfeld surface analyses were performed to examine intermolecular interactions within the crystal structures of Fe–X. Hirshfeld volumes and surfaces for Fe–Br and Fe–I are smaller than those for Fe–F and Fe–Cl, suggesting that the longer Fe–Br and Fe–I bonds influence the transition to the monoclinic crystal system with denser packing.