Abstract
A redox-switchable self-assembled ZnII 4 L6 cage was synthesized that contains naphthalenediimide (NDI) motifs. Its reduction lent these NDI panels persistent radical anion character. The redox activity of this cage allows it to act as a catalyst for the oxidative coupling of different tetraaryl borates to give biaryls. The catalytic activity of the cage was enhanced following its binding of C60 , which implies a mechanism that does not involve encapsulation of the substrate.
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