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

High Resolution Image Download MS PowerPoint Slide Neutral Te(II) species 2-( t BuNCH)C 6 H 4 TeCl ( [I]Cl ) as well as tellurenyl Te(II) + cations [2-( t BuNCH)C 6 H 4 Te][X] (X = OTf or SbF 6 ), i.e., [I][OTf] and [I][SbF 6 ], 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][SbF 6 ] 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 (Et 3 SiH, Ph 3 SiH, Ph 2 SiH 2, and (EtO) 3 SiH) 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.