Structure and Photoinduced Electron Transfer Dynamics of a Series of Hydrogen-Bonded Supramolecular Complexes Composed of Electron Donors and a Saddle-Distorted Diprotonated Porphyrin

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• 作者：Tatsuhiko Honda ; Tatsuaki Nakanishi ; Kei Ohkubo ; Takahiko Kojima ; Shunichi Fukuzumi
• 刊名：Journal of the American Chemical Society
• 出版年：2010
• 出版时间：July 28, 2010
• 年：2010
• 卷：132
• 期：29
• 页码：10155-10163
• 全文大小：337K
• 年卷期：v.132,no.29(July 28, 2010)
• ISSN：1520-5126

文摘

The excited-state photodynamics of intrasupramolecular photoinduced electron transfer was investigated in a series of hydrogen-bonded supramolecular complexes composed of diprotonated 2,3,5,7,8,10,12,13,15,17,18,20-dodecaphenylporphyrin (H₄DPP²⁺) and electron donors bearing a carboxylate group. The formation of supramolecular complexes was examined by spectroscopic measurements. The binding constants obtained by spectroscopic titration indicate the strong binding (10⁸−10¹⁰ M⁻²) even in a polar and coordinating solvent, benzonitrile (PhCN). The crystal structure of the supramolecular assembly using ferrocenecarboxylate (FcCOO⁻) was determined to reveal a new structural motif involving two-point and single-point hydrogen bonding among saddle-distorted H₄DPP²⁺ dication and two FcCOO⁻ anions. Femtosecond laser flash photolysis was applied to investigate the photodynamics in the hydrogen-bonded supramolecular complexes. Rate constants obtained were evaluated in light of the Marcus theory of electron transfer, allowing us to determine the reorganization energy and the electronic coupling matrix constant of photoinduced electron transfer and back electron transfer to be 0.68 eV and 43 cm⁻¹, respectively. The distance dependence of electron transfer was also examined by using a series of ferrocenecarboxylate derivatives connected by linear phenylene linkers, and the distance dependence of the rate constant of electron transfer (k_ET) was determined to be k_ET = k₀ exp(−βr), in which β = 0.64 Å⁻¹.