Porphyrin–BODIPY-based hybrid model compounds for artificial photosynthetic reaction centers

Abstract

In this review, we report the synthesis and photophysical studies of porphyrin–4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) compounds linked either with different covalent bonds or with axial coordination to metalloporphyrin. BODIPY moiety significantly increases the light absorption capability of porphyrins by efficient BODIPY to porphyrin excitation energy transfer. The type of linkage between the two chromophores significantly affects the energy transfer efficiency. The most efficient energy transfer was proved for compounds linked via a cyanuric chloride bridge (∼99% quenching). Therefore, this type of bond seems to be more appropriate choice in constructing porphyrin–BODIPY assemblies for light harvesting applications. Moreover, the functionalization of the conjugates with fullerenes appears to be interesting electron transfer dynamics in the excited state.