The reaction chemistry of metalla-aromatics is fundamentally interesting. In this work, we find that tetralithio spiroaromatic palladole and platinacycle complexes 1 undergo selective two-electron oxidation with 1,2-dibromoethane as a mild… Click to show full abstract
The reaction chemistry of metalla-aromatics is fundamentally interesting. In this work, we find that tetralithio spiroaromatic palladole and platinacycle complexes 1 undergo selective two-electron oxidation with 1,2-dibromoethane as a mild oxidant, affording their corresponding dilithio spiro metallacyclopentadienes 3. These dilithio spiro complexes 3 can be reductively transformed to their corresponding tetralithio spiroaromatic complexes 1 with metallic lithium. When treated with an appropriate amount of oxidants, both 1 and 3 can generate 1,4-dihydropentalene derivatives 5 via a mechanism involving reductive elimination and silyl migration, as supported by density functional theory calculation. Similarly, tetralithio aromatic dicupra[10]annulene 2 can also undergo the reversible two-electron redox reaction mentioned above. These results improve our understanding of the reactivity of metalla-aromatic compounds.
               
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