Highly reducible π-extended copper corroles

Abstract

Di- and octa-phenylethynyl (PE) substituted π-extended copper corroles were synthesized and characterized as to their structural, electrochemical and spectroscopic properties. The addition of two or eight PE groups to the β-pyrrole positions of the corrole results in dramatic red shifts in the electronic absorption spectra and new reductions which are not seen for the parent compound lacking PE substituents. CuCor(PE)₈ is reduced in four reversible one-electron transfer steps to give derivatives of [CuCor(PE)₈]ⁿ⁻ where n = 1, 2, 3 or 4. Variable temperature ¹H NMR and EPR measurements were carried out and suggest that the octa- and di-PE substituted Cu-corroles can both be described as an antiferromagnetically coupled Cu^II corrole cation radical which is in equilibrium with a triplet state, possibly due to a lower singlet–triplet energy gap as compared to 1 and 2 at room temperature. The EPR spectra of one-electron oxidized and one electron reduced species exhibited the characteristics of Cu(II) corroles. The products generated in the first two reductions of each π-extended corrole were characterized by thin-layer spectroelectrochemistry, thus providing new insights into how UV-vis spectra of highly reduced corroles vary as a function of the number of PE groups and overall charge on the molecule. The singly reduced and singly oxidized copper corroles were also chemically generated in CH₃CN and shown to have UV-visible spectra almost identical to the spectra obtained by electroreduction or electrooxidation in PhCN or THF containing 0.1 M tetrabutylammonium perchlorate.