Decatungstate Anion for Photocatalyzed "Window Ledge" Reactions.

The majority of organic reactions are commonly carried out inside a lab, under a fume hood. A particular case is that of photochemical reactions, a field where the pioneering experiments by Giacomo Ciamician demonstrated more than one century ago that different processes can be carried out outdoors, for example, on the balcony of his own department, upon exposure of the reacting mixtures to sunlight. The main problem related to this chemistry of the "window ledge" is that most organic compounds are colorless and their absorption in the solar light region is in most cases negligible. Recently, the impressive development in the use of visible light absorbing photocatalysts (e.g., Ru or Ir complexes, as well as organic dyes) made light-induced processes convenient even for non-photochemistry practitioners. It is thus possible to easily perform the reactions by simply placing the reaction vessel in a sunny place outside the lab. However, most of these processes are based on single electron transfer (SET) reactions (photoredox catalysis). Other photocatalysts able to activate substrates via alternative paths, such as hydrogen atom transfer (HAT), are emerging. In the last years, we were deeply involved in the use of the decatungstate anion ([WO], a polyoxometalate) in synthesis. Indeed, such a versatile species is able to promote the photocatalytic C-H activation of organic compounds via either SET or HAT reactions. Interestingly, though the absorption spectrum of [WO] does not extend into the visible region, it shows an overlap with solar light emission. In this Account, we provide an overview on the application of decatungstate salts as photocatalysts in window ledge chemistry. We initially discuss the nature of the photogenerated species involved in the mechanism of action of the anion, also supported by theoretical simulations. The first-formed excited state of the decatungstate anion decays rapidly to the active species, a dark state tagged wO, featuring the presence of electron-deficient oxygen centers. Next, we describe the main applications of decatungstate chemistry. A significant part of this Account is devoted to photocatalyzed synthesis (C-X bond formation, with X = C, N, O, and oxidations) carried out by adopting sunlight (or simulated solar light). This synthetic approach is versatile, and most of the reactions involved C-H activation in cycloalkanes, alkylaromatics, amides, ethers (1,4-dioxane, oxetane, benzodioxole, and THF), aldehydes, nitriles, and cyclopentanones, and the ensuing addition of the resulting radicals onto electron-deficient olefins. Finally, the increasing role of the decatungstate anion in water depollution and polymerization is briefly discussed.