Subphthalocyanine capsules: molecular reactors for photoredox transformations of fullerenes

Abstract

The internal cavity formed by a dimeric subphthalocyanine (SubPc) capsule (SubPc₂Pd₃, 2), ensembled by coordination of pyridyl substituents in the monomeric SubPc 1 to Pd centers, has proved an optimal space for the complexation of C₆₀ fullerene. Taking advantage of the intense absorption of green light of the SubPc component at around 550 nm, we have tested different green-light induced photoredox addition reactions over the double bonds of guest C₆₀. Both addition of amine radicals, generated by reductive quenching of the excited state of 2 by aromatic trimethylsilylamines, and addition of trifluoroethyl radicals, obtained from oxidative quenching of the photosensitizer, have successfully taken place with good yields in the 2:C₆₀ host:guest complex. On the other hand, both the photoredox reactions result in much lower yields when the monomeric pyridyl-SubPc is used as a photocatalyst, demonstrating that encapsulation results in a strong acceleration of the reaction. Importantly, this is the first example of the use of a confined microenvironment to trigger photoredox chemical transformations of fullerenes.