Single hydroxo-bridged group 13 metalloporphyrin dimers: Solution studies and solid-state structures

Abstract

The syntheses of indium, gallium and aluminum porphyrin dimers with a single hydroxo-bridge, [Formula: see text][M(Porph)]2(OH)[Formula: see text], are described. Emphasis is given to indium and gallium derivatives. The X-ray structures for [Formula: see text] [Ga(OEP)]2(OH)[Formula: see text] ClO4 and [Formula: see text] [In(OEP)]2(OH)[Formula: see text] ClO4 (two forms) are presented. The dimeric molecules can be synthesized by the acid-treatment of the corresponding hydroxo-ligated monomeric complexes [M(OEP)(OH)] and [M(TPP)(OH)]. The nature of the starting material (the hydroxo-ligated monomer) was first suggested by IR spectroscopy and further proved by proton-deuterium exchange followed by 1H NMR spectroscopy. The structure of a monomeric indium hydroxide complex, [In(OEP)(OH)], is also presented. The synthesis of the dimer for all metals can be monitored by UV-vis spectroscopy, which clearly demonstrates that a blue-shift of the Soret band accompanies formation of the dimer from the monomer. A strong [Formula: see text]–[Formula: see text]interaction between the two porphyrin rings of these [Formula: see text]-hydroxo-bridged dimers is confirmed both by solution state studies (1H NMR and UV-vis spectroscopy) and the X-ray structures of [Formula: see text] [M(OEP)]2(OH)[Formula: see text] ClO4 (M = In, Ga). In addition, exposure of methylene chloride solutions of these bridged complexes to white light afforded the corresponding chloro derivatives, [M(Porph)Cl]. The stereochemistry of a range of [Formula: see text]-hydroxo dimers is discussed and DFT simulations at the HSEH1PBE/SDD level of theory provide suitable structural models and further electronic structure insights on selected [Ga(Porph)(OH)] and [Formula: see text] [Ga(Porph)]2(OH)[Formula: see text][Formula: see text] derivatives.