A Substrate-Dependent Redox Catalysis of Tellurenyl Species Involving Oxidation States +I, +II, and +IV

Neutral Te(II) species 2-(tBuNCH)C6H4TeCl ([I]Cl) as well as tellurenyl Te(II)+ cations [2-(tBuNCH)C6H4Te][X] (X = OTf or SbF6), i.e., [I][OTf] and [I][SbF6], exhibit a wide range of reactivity toward various ortho-quinones. While the reaction of ortho-chloranil leads to the oxidation of Te(II) into Te(IV), 3,5-di-tert-butyl-ortho-benzoquinone leads only to partial oxidation due to an ongoing dynamic reversible reaction, being the first example of a chemically reversible two electron Te(II)/Te(IV) redox couple. By contrast, 9,10-phenanthrenequinone as a very weak oxidant shows no reaction; however, the most Lewis acidic [I][SbF6] produces a corresponding Lewis adduct interacting by both electrostatic and weak chalcogen bond interactions. The diverse reactivity scope is further complemented by DFT computed thermochemistry data. Furthermore, [I][OTf] is successfully utilized for the catalytic transfer of silanes (Et3SiH, Ph3SiH, Ph2SiH2, and (EtO)3SiH) to ortho-quinones via redox single or double Si–H bond activation, yielding silylated catechols, monomeric cyclic catecholatosilanes, or bis(catecholato)silanes. Surprisingly, in the absence of the catalyst [I][OTf], the reactivity spans from no reaction to the formation of hexachloro-dibenzo[1,4]dioxine-2,3-dione. The latter product is an entirely different substance class compared to the one formed during the catalyzed reaction.