TY - JOUR
T1 - Co-facial magnesium porphyrin dimer complexed with fullerene
T2 - Photosynthetic reaction center model of 'special pair' self-assembled to electron acceptor
AU - Sandanayaka, Atula S.D.
AU - Subbaiyan, Navaneetha K.
AU - Chitta, Raghu
AU - Araki, Yasuyuki
AU - Ito, Osamu
AU - D'Souza, Francis
PY - 2008
Y1 - 2008
N2 - Using a self-assembled supramolecular approach, a closer model for the photosynthetic reaction center 'special pair' assembled with an electron acceptor conjugate, is reported. As the 'special pair' donor, magnesium meso-(benzo-15-crown-5)porphyrin was self-assembled with K+ to form a highly stable Mg porphyrin dimer with a co-facial geometry arrangement, which is a better electron donor since it is nearly 130 mV easier to oxidize compared to the earlier reported Zn porphyrin dimer analog. Further, pyridine and alkyl ammonium cation-functionalized fullerene was attached via axial coordination and crown ether-alkyl ammonium cation complexation to form the four-fold, donor-acceptor complex. The self-assembled supramolecular complex, constructed using this approach, possesses defined geometry and orientation. Efficient charge separation from the singlet excited state of the Mg porphyrin dimer to the fullerene entity and a relatively slow charge recombination, were revealed by time-resolved emission and nanosecond transient absorption spectral studies, supporting the impending exploitation of these novel biomimetic model systems for light energy harvesting applications.
AB - Using a self-assembled supramolecular approach, a closer model for the photosynthetic reaction center 'special pair' assembled with an electron acceptor conjugate, is reported. As the 'special pair' donor, magnesium meso-(benzo-15-crown-5)porphyrin was self-assembled with K+ to form a highly stable Mg porphyrin dimer with a co-facial geometry arrangement, which is a better electron donor since it is nearly 130 mV easier to oxidize compared to the earlier reported Zn porphyrin dimer analog. Further, pyridine and alkyl ammonium cation-functionalized fullerene was attached via axial coordination and crown ether-alkyl ammonium cation complexation to form the four-fold, donor-acceptor complex. The self-assembled supramolecular complex, constructed using this approach, possesses defined geometry and orientation. Efficient charge separation from the singlet excited state of the Mg porphyrin dimer to the fullerene entity and a relatively slow charge recombination, were revealed by time-resolved emission and nanosecond transient absorption spectral studies, supporting the impending exploitation of these novel biomimetic model systems for light energy harvesting applications.
KW - Biomimicry
KW - Fullerene
KW - Magnesium porphyrin
KW - Photoinduced electron transfer
KW - Synthetic reaction center
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U2 - 10.1142/S108842460800025X
DO - 10.1142/S108842460800025X
M3 - Article
AN - SCOPUS:52449132026
SN - 1088-4246
VL - 12
SP - 857
EP - 865
JO - Journal of Porphyrins and Phthalocyanines
JF - Journal of Porphyrins and Phthalocyanines
IS - 7
ER -