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Volumn 213, Issue 1, 2010, Pages 73-79

Effects of hydrogen bonding interaction and solvent polarity on the competition between excitation energy and photo-induced electron transfer processes in hydroxy(1-pyrenebutoxy)phosphorus(V)porphyrin

Author keywords

Electron transfer; Energy transfer; Hydrogen bonding; Phosphorus(V)porphyrin; Pyrene; Solvent effect

Indexed keywords


EID: 77953324792     PISSN: 10106030     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jphotochem.2010.05.002     Document Type: Article
Times cited : (15)

References (43)
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    • The CT state energy in solvent x (ECT)x was calculated from the following equation: (ECT)x, ECT)m, e2, 4 π ε{lunate}0, 1, ε{lunate}x, 1, ε{lunate}m, 1, 2 rpy) where (ECT)m is the CT state energy in solvent m, e is the electronic charge, εx, and εm are the static dielectric constants of solvent x and m, respectively, and rpy is the ionic radius of the pyrene moiety (4.0 Å, This radius was estimated from the ab initio MO calculation. Because the positive charge on the P(V) porphyrin ring is neutralized by the ELT, the factors of the ionic radius of the porphyrin ring and the distance between the pyrene and porphyrin moieties were negligible
    • py is the ionic radius of the pyrene moiety (4.0 Å). This radius was estimated from the ab initio MO calculation. Because the positive charge on the P(V) porphyrin ring is neutralized by the ELT, the factors of the ionic radius of the porphyrin ring and the distance between the pyrene and porphyrin moieties were negligible.
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    • py). According to the above mentioned reason, the factors of the porphyrin ionic radius and the distance between the pyrene and porphyrin moieties were neglected.
    • py). According to the above mentioned reason, the factors of the porphyrin ionic radius and the distance between the pyrene and porphyrin moieties were neglected.


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