Controlling the Diradical Character of Thiele Like Compounds.

Organic diradicals play an important role in many fields of chemistry, biochemistry, and materials science. In this work, by means of high-level theoretical calculations, we have investigated the effect of representative chemical substituents in -quinodimethane (QDM) and Thiele's hydrocarbons with respect to the singlet-triplet energy gap, a feature characterizing their diradical character. We show how the nature of the substituents has a very important effect in controlling the singlet-triplet energy gap so that several compounds show diradical features in their ground electronic state. Importantly, steric effects appear to play the most determinant role for QDM analogues, with minor effects of the substituents in the central ring. For Thiele like compounds, we found that electron-withdrawing groups in the central ring favor the quinoidal form with a low or almost null diradical character, whereas electron-donating group substituents favor the aromatic-diradical form if the electron donation does not exceed 6-π electrons. In this case, if there is an excess of electron donation, the diradical character is reduced. The electronic spectrum of these compounds is also calculated, and we predict that the most intense bands occur in the visible region, although in some cases characteristic electronic transition in the near-IR region may appear.