Highly Efficient Photoproduction of Charge-Separated States in Donor−Acceptor-Linked Bis(acetylide) Platinum Complexes
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文摘
We report a highly efficient charge separation system, D−Pt−A, where D (triphenylamine) and A (naphthalenediimide) are bonded to the Pt moiety through highly twisted phenylene ethynylene linkages. The quantum yields for the formation of the charge-separated state were determined to be nearly unity. The lifetimes of D+−Pt−A were 1 μs at room temperature and much longer at low temperature. The spin-correlated radical ion pair was directly observed by means of time-resolved EPR spectroscopy.
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