Nitronyl Nitroxide Bifunctionalized Electron-Poor Chromophores: Synthesis of Stable Dye Biradicals by Lewis Acid Promoted Desilylation.

Open shell organic molecules bearing π-cores are of great interest for optical, electronic, and magnetic applications but frequently suffer fast decomposition or lack synthetic accessibility. In this regard, nitronyl nitroxides are promising candidates for stable (bi-)radicals due to their high degree of spin delocalization along the O-N-C-N-O pentad unit. Unfortunately, they are limited to electron-rich systems so far. To overcome this limitation, we developed a synthetic procedure for the twofold spin decoration of electron-poor chromophores ( = -1158 mV) with nitronyl nitroxide radical moieties via selective deprotection/oxidation of the respective silylated precursors with boron fluoride and subsequent quenching with tetraethyl orthosilicate. Nitronyl nitroxide biradicals PBI-NN, IIn-NN, PhDPP-NN, ThDPP-NN, and FuDPP-NN bridged by perylene bisimide (PBI), isoindigo (IIn), and diketopyrrolopyrrole (DPP) pigment colorants were finally obtained as bench stable compounds after periodate oxidation with yields of 60-81%. The absorption spectral signatures of the chromophores remain preserved in the open shell state and match the ones of the pristine parent compounds, which allowed an prediction of their optical properties. Consequently, we achieved twofold spin labeling while keeping the intrinsic properties of the electron deficient chromophores intact.