The Planar Cyclooctatetraene Bridge in Bis-Metallic Macrocycles: Isolating or Conjugating?

Abstract

A minor modification of the reported procedure for the synthesis of a corrole dimer that is fused by the cyclooctatetraene (COT) unit, (H3tpfc)2COT, allowed for its isolation in 18% yield. Of the two redox isomers that this interesting macrocycle does form, the current focus is on the reduced form, in which each subunit resembles that of monomeric corroles with a trianionic N4 coordination core. The corresponding bis-gallium(III) complex was prepared as an entry into the potentially rich coordination chemistry of (H3tpfc)2COT. Both X-ray crystallography and DFT calculations disclosed that the COT moiety is essentially planar with very unusual nonalternating C-C bonds. The same holds true for the bis-gallium(III) complexes [(Ga-tpfc)2]COT(py)2 and [(Ga-tpfc)2]COT(py)4, obtained with one and two pyridine molecules coordinated to each metal ion, respectively. The electronic spectra of both the free base and the gallium(III) complexes display an extremely low energy band (λmax at 720-724 nm), which points toward extensive π delocalization through the COT bridge. This aspect was fully addressed by examining the interactions between the two corrole subunits in terms of electrochemistry and DFT calculations of the oxidized and reduced macrocycle. The new near-IR bands that appear upon both oxidation (λmax 1250 nm) and reduction (λmax 1780 nm) serve as additional supporting evidence for this conclusion.