Methanofullerene-Based Palladium Bis(amino)aryl Complexes and Application in Lewis Acid Catalysis

Synthetic routes have been developed for the attachment of palladium(II) bis(amino)aryl (NCN or C 6 H 2 {CH 2 NMe 2 } 2 -2,6) - complexes to C 60 . Using diazo and Bingel addition reactions, various methanofullerene NCN−SiMe 3 compounds (C 60 −L−NCN−SiMe 3, L = C(Me), C(CO 2 Et)CO 2 CH 2, and C(Me)C 6 H 4 C⋮C) have been prepared and characterized. Electrophilic palladation of these ligands was achieved with Pd(OAc) 2, leading to the corresponding C 60 −L−NCN·PdCl complexes. These were converted into active Lewis acid catalysts for the aldol condensation and the Michael reaction. Catalytic tests show that the activity of cationic methanofullerene NCN−palladium complexes in the aldol reaction between benzaldehyde and methyl isocyanoacetate is comparable to the parent unsupported NCN palladium complex. However, in the Michael reaction of methyl vinyl ketone and ethyl cyanoacetate, the fullerene catalysts are not only significantly slower but also undergo a deactivation/decomposition process during the reaction. Preliminary retention measurements using a nanofiltration membrane have shown 72% retention of the palladium complex C 60 −C(Me)−(NCN)PdCl.