期刊
JOURNAL OF PHYSICAL CHEMISTRY A
卷 106, 期 10, 页码 2036-2048出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp012133s
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A highly efficient functional mimic of a photosynthetic antenna-react ion center complex has been designed, synthesized, and studied spectroscopically. The antenna, consisting of four covalently linked zinc tetraarylporphyrins, (P-ZP)(3)-Pzc, has been coupled to a free-base porphyrin-fullerene artificial photosynthetic reaction center, P-C-60, to form a (P-ZP)(3)-P-ZC-P-C-60 hexad. As revealed by time-resolved absorption and emission studies in 2-methyltetrahydrofuran solution at ambient temperature, excitation of a peripheral zinc porphyrin moiety is followed by singlet-singlet energy transfer to the central zinc porphyrin to give (P-ZP)(3)-P-1(ZC)-P- C-60 with a time constant of 50 ps. The excitation is passed on to the free-base porphyrin in 32 ps to produce (P-ZP)(3)-P-ZC-P-1-C-60, which decays by electron transfer to the fullerene with a time constant of 25 ps. The resulting (P-ZP)(3)-P-ZC-P.+-C-60(.-) charge-separated state is generated with a quantum yield of 0.98 based on light absorbed by the porphyrin antenna. Direct excitation of the free-base porphyrin moiety or the fullerene also generates this state with a yield near unity. Thermodynamically favorable migration of positive charge the zinc porphyrin array transforms the initial state into a long-lived ((P-ZP)(3)-P-ZC)(.+)-P-C60.- charge-separated state with a time constant of 380 ps. The final charge-separated state, formed in high yield (similar to0.90), decays to the ground state with a lifetime of 240 ns. In benzonitrile, the lifetime is 25 mus. A previous hexad, which differs from the current hexad solely in the nature of the free-base porphyrin, gave a charge-separated state with a lower yield (0.69) and a shorter lifetime (1.3 ns). The difference in performance is attributed to differences in electronic composition (a(2u) versus a(1u) HOMO), conformation, and oxidation potential (1.05 versus 0.84 V) between the meso-tetraarylporphyrin and the beta-octaalkylporpliyrin of the current and former hexads, respectively. These results can be explained on the basis of an understanding of factors that affect through-bond energy-transfer and electron-transfer processes. The results demonstrate that it is possible to design and prepare synthetic, porphyrin-based antenna-reaction center complexes that mimic the basic photochemical functions of natural photosynthetic light-harvesting antenna, and reaction centers in simple, structurally well-defined constructs.
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