Résumé
We describe the preparation of six diketones based on the frameworks of five bis-naphthoporphyrins and one perinaphthoporphyrin. All diketones derive from meso-tetraarylporphyrins having incorporated two carbonyl groups, each one connected to one beta-pyrrole carbon and one ortho carbon atom from a meso-aryl group. These compounds were all produced in good yield by intramolecular Friedel-Crafts acylation, either from porphyrins meso-substituted by o-carboxyphenyl or o,o'-dicarboxyphenyl substituents or from porphyrins bearing carboxy groups attached to the pyrrolic beta-positions. Although the former reaction does not show significant regioselectivity when run on nickel complexes, the opposite is true for the corresponding free bases. All diketones show a spectacular bathochromic shift of the UV-vis absorption, the longest wavelength bands absorbing in the 700-825 nm range. Two compounds were structurally characterized by X-ray diffraction. In the case of the diketone, whose carbonyl groups are attached to vicinal pyrrolic beta-positions, a significant intermolecular interaction between the two carbonyl groups and an aromatic hydrogen atom was detected.