Photoinduced charge shift and charge recombination through an alkynyl spacer for an expanded acridinium-based dyad
Literature Information
Andrew C. Benniston, Jerry Hagon, Xiaoyan He, Helge Lemmetyinen, Nikolai V. Tkachenko, William Clegg, Ross W. Harrington
The photophysical and electrochemical properties of a dyad comprising an expanded acridinium light-harvester, coupled via a triple bond to a trialkyloxybenzene donor, are described. Laser excitation of the dyad in 1,2-dichloroethane (DCE) results in rapid charge shift (5 ps) followed by slower charge recombination (81 ps) to completely restore the ground state. Discrimination between forward and return electron transfer (kret/kfor ∼ 16) is rather poor. There is no indication of triplet formation on the expanded acridinium-based group following charge recombination.
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