The electronic structure of copper corroles has been
a topic of
debate and revision since the advent of corrole chemistry. The ground
state of these compounds is best described as an antiferromagnetically
coupled Cu(II) corrole radical cation. In coordinating solvents, these
molecules become paramagnetic, and this is often accompanied by a
color change. The underlying chemistry of these solvent-induced properties
is currently unknown. Here, we show that a coordinating solvent, such
as pyridine, induces a change in the ground spin state from an antiferromagnetically
coupled Cu(II) corrole radical cation to a ferromagnetically coupled
triplet. Over time, the triplet reacts to produce a species with spectral
signatures that are characteristic of the one-electron-reduced Cu(II)
corrole. These observations account for the solvent-induced paramagnetism
and the associated color changes that have been observed for copper
corroles in coordinating solvents