Abstract
The 2-bit Lindqvist-type polyoxometalate (POM) [V(6)O(13)((OCH(2))(3)CCH(2)N(3))(2)](2-) with a diamagnetic {V(6)O(19)} core and azide termini shows six fully oxidized V(V) centers in solution as well as the solid state, according to (51)V NMR spectroscopy. Under UV irradiation, it exhibits reversible switching between its ground S(0) state and the energetically higher lying states in acetonitrile and water solutions. TD-DFT calculations demonstrate that this process is mainly initialized by excitation from the S(0) to S(9) state. Pulse radiolysis transient absorption spectroscopy experiments with a solvated electron point out photochemically induced charge disproportionation of V(V) into V(IV) and electron communication between the POM molecules via their excited states. The existence of this unique POM-to-POM electron communication is also indicated by X-ray photoelectron spectroscopy (XPS) studies on gold-metalized silicon wafers (Au//SiO(2)//Si) under ambient conditions. The amount of reduced vanadium centers in the "confined" environment increases substantially after beam irradiation with soft X-rays compared to non-irradiated samples. The excited state of one POM anion seems to give rise to subsequent electron transfer from another POM anion. However, this reaction is prohibited as soon as the relaxed T(1) state of the POM is reached.