Abstract
Organolithium compounds can behave as reductants but never as oxidants in redox reactions. Reported herein is that 1,4-dilithio-1,3-butadienes reacted with [Ni(cod)2] (cod = 1,5-cyclooctadiene) to deliver dilithionickeloles. Single-crystal X-ray structural analysis revealed a coplanar structure of dilithionickeloles with an averaging of bond lengths. XPS data confirmed the oxidation state of Ni in dilithionickeloles was Ni(2+). (7)Li NMR spectra of dilithionickeloles and theoretical calculations revealed a considerable aromatic character. In this redox reaction, the dilithio dianionic compounds behaved as formal oxidants, thus oxidizing Ni(0) into Ni(2+). These results demonstrated that organolithium compounds with π-conjugation could be used as oxidants and could continue to accept extra electrons.
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