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Thermodynamics and Photodynamics of a Monoprotonated Porphyrin Directly Stabilized by Hydrogen Bonding with Polar Protic Solvents

Title
Thermodynamics and Photodynamics of a Monoprotonated Porphyrin Directly Stabilized by Hydrogen Bonding with Polar Protic Solvents
Authors
Suzuki, WataruKotani, HiroakiIshizuka, TomoyaOhkubo, KeiShiota, YoshihitoYoshizawa, KazunariFukuzumi, ShunichiKojima, Takahiko
Ewha Authors
Shunichi Fukuzumi
SCOPUS Author ID
Shunichi Fukuzumiscopus
Issue Date
2017
Journal Title
CHEMISTRY-A EUROPEAN JOURNAL
ISSN
0947-6539JCR Link1521-3765JCR Link
Citation
vol. 23, no. 19, pp. 4669 - 4679
Keywords
hydrogen bondsmonoprotonated porphyrinsnonplanar porphyrinselectron transferpolar protic solvents
Publisher
WILEY-V C H VERLAG GMBH
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
Addition of 1equiv of TFA to an acetone solution containing dodecaphenylporphyrin (H2DPP) in the presence of 10% MeOH (v/v) resulted in selective formation of a monoprotonated form (H3DPP+), in sharp contrast to protonation of H2DPP directly affording a diprotonated form (H4DPP2+) in acetone in the absence of MeOH. The crucial role of MeOH for selective H3DPP+ formation was interpreted as hydrogen-bonding stabilization of H3DPP+, since a MeOH molecule was found to form hydrogen bonds with an NH proton of H3DPP+ in the crystal. The selectivity of H3DPP+ formation was evaluated by the formation yield of H3DPP+, which increased when elevating the portion of MeOH (0-10%) in acetone with saturation behavior, suggesting that H3DPP+ is stabilized by hydrogen bonding with MeOH even in solution, together with the thermodynamic parameters determined from a van't Hoff plot based on the spectroscopic titration. Femto- and nanosecond laser flash photolysis allowed us to elucidate the photodynamics of H3DPP+ in intermolecular photoinduced electron transfer (ET) from ferrocene derivatives as one-electron donors to the triplet excited state of H3DPP+ as an electron acceptor. The second-order rate constants of the ET reactions were evaluated in light of the Marcus theory of ET. The reorganization energy of ET was determined to be 1.87eV, which is slightly larger than that of H4DPP2+ in acetonitrile (1.69eV), due to larger structural change upon ET than that of H4DPP2+.
DOI
10.1002/chem.201606012
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자연과학대학 > 화학·나노과학전공 > Journal papers
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