Abstract
AbstractIn this review, we address recent studies of porphyrin‐based molecular systems for efficient singlet oxygen (1O2) generation. Porphyrins have a highly conjugated, delocalized 18‐π electron system (for the shortest cyclic path) that is responsible for the strong absorption and emission characteristics in the visible region. Singlet oxygen is useful for applications in photodynamic cancer therapy (PDT), photooxidation of toxic molecules, and photoproduction of important intermediates for various chemicals owing to its high oxidation ability. Porphyrin and its analogues have been investigated as photosensitizers for 1O2 generation. The production of 1O2 is successfully regulated by photophysical parameters, such as intersystem crossing, triplet state (T1) lifetime, and photosensitizer to 3O2 energy transfer in molecular systems. Introduction of substituents with heavy atoms (halogen, metal) and radicals onto the photosensitizer (PS) exerts a strongly positive impact on intersystem crossing of the singlet excited state of the PS, promoting generation of the triplet excited state. Environmental conditions, such as solvent and pH, may also influence 1O2 generation. As a means to limit cellular photodamage, two‐photon absorption and DNA switches for 1O2 generation have been proposed and developed. Achieving control of singlet oxygen generation is pertinent to many arenas at the cutting edge of modern science, ranging from the chemical industry to biomedical applications.
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