In this work, we aimed to develop a dicyanomethyl radical that undergoes both reversible C-C bond formation/dissociation and metal-ligand coordination reactions to combine dynamic covalent chemistry (DCC) based on organic radicals with coordination chemistry. We have previously reported a dicyanomethyl radical conjugated with a triphenylamine (1⋅) that exhibits a monomer/dimer equilibrium between the σ-bonded dimer (12 ). We designed and synthesized a novel dicyanomethyl radical with a pyridyl group as a coordination point (2⋅) by replacing the phenyl group of 1⋅ with a 3-pyridyl group. We showed that 2⋅ is also in an equilibrium with the σ-bonded dimer (22 ) in solution and has suitable thermodynamic parameters for application in DCC. 22 coordinates to PdCl2 in a 2 : 2 ratio to selectively form a metallamacrocycle (22 )2 (PdCl2 )2 , and its structure was clarified by single crystal X-ray analysis. Variable-temperature NMR, ESR, and electronic absorption measurements revealed that (22 )2 (PdCl2 )2 also undergoes the reversible C-C bond formation/dissociation reaction. Ligand-exchange experiment showed that 22 was liberated from (22 )2 (PdCl2 )2 by the addition of another ligand with a higher affinity for PdII . This work demonstrated that DCC based on dicyanomethyl radicals works orthogonally to metal-ligand coordination reactions.
Keywords: Coordination Chemistry; Dynamic Covalent Chemistry; Macrocyclic Complex; Organic Radical; Self-Assembly.
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