Directly Connected AzaBODIPY-BODIPY Dyad: Synthesis, Crystal Structure, and Ground- and Excited-State Interactions

摘要

Directly connected, strongly interacting sensitizer donor-acceptor dyads mimic light-induced photochemical events of photosynthesis. Here, we devised a dyad composed of BF2-chelated dipyrromethene (BODIPY) directly linked to BF2-chelated tetraarylazadipyrromethene (azaBODIPY) through the beta-pyrrole position of azaBODIPY. Structural integrity of the dyad was arrived from two-dimensional NMR spectral studies, while single-crystal X-ray structure of the dyad provided the relative orientation of the two macrocycles to be similar to 62 degrees. Because of direct linking of the two entities, ultrafast energy transfer from the (BODIPY)-B-1* to azaBODIPY was witnessed. A good agreement between the theoretically estimated Forster energy transfer rate and experimentally determined rate was observed, and this rate was found to be higher than that reported for BODIPY-azaBODIPY analogues connected with spacer units. In agreement with the free-energy calculations, the product of energy transfer, (1)azaBODIPY* revealed additional photochemical events such as electron transfer leading to the creation of BODIPY center dot+-azaBODIPY(center dot-) radical ion pair, more so in polar benzonitrile than in nonpolar toluene, as evidenced by femtosecond transient spectroscopic studies. Additionally, the spectral, electrochemical, and photochemical studies of the precursor compound azaBODIPY-dipyrromethane also revealed occurrence of excited-state events. In this case, electron transfer from the (1)azaBODIPY* to dipyrromethane (DPM) yielded DPM center dot+-azaBODIPY(center dot-) charge-separated state. The study described here stresses the role of close association of the donor and acceptor entities to promote ultrafast photochemical events, applicable of building fast-response optoelectronic and energy-harvesting devices.