摘要： This contribution details an efficient and controlled photopolymerization regulated by far-red (λ = 680 nm) and NIR (λ = 780 and 850 nm) light in the presence of aluminum phthalocyanine and aluminum naphthalocyanine. Initiating radicals are generated by photosensitization of peroxides affording an effective strategy that provides controlled polymerizations of a variety of monomers with excellent living characteristics. Critically, long wavelength irradiation provides penetration through thick barriers, affording unprecedented rates of controlled polymerization that can open new and exciting applications. Furthermore, a more optimized approach to performing solar syntheses is presented. By combining the narrow Q-bands of these PCs with others possessing complementary absorptions, layered, independent polymerizations and organic transformations may be performed in parallel under a single broadband emission source such as sunlight.