Photoinitiated Charge Transport through π-Stacked Electron Conduits in Supramolecular Ordered Assemblies of Donor-Acceptor Triads

被引:104
作者
Bullock, Joseph E.
Carmieli, Raanan
Mickley, Sarah M.
Vura-Weis, Josh
Wasielewski, Michael R. [1 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
关键词
X-RAY-SCATTERING; PHOTOSYNTHETIC REACTION-CENTER; EXCITED-STATE PHOTODYNAMICS; RANDOMLY ORIENTED MOLECULES; CORRELATED RADICAL PAIRS; FIELD-EFFECT TRANSISTORS; LIGHT-HARVESTING ARRAYS; PERYLENE BISIMIDE DYES; SMALL-ANGLE SCATTERING; ENERGY-TRANSFER;
D O I
10.1021/ja903903q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Photochemical electron donor-acceptor triads having an aminopyrene primary donor (APy) and a p-diaminobenzene secondary donor (DAB) attached to either one or both imide nitrogen atoms of a perylene-3,4:9,10-bis(dicarboximide) (PDI) electron acceptor were prepared to give DAB-APy-PDI and DAB-APy-PDI-APy-DAB. In toluene, both triads are monomeric, but in methylcyclohexane, they self-assemble into ordered helical heptamers and hexamers, respectively, in which the PDI molecules are pi-stacked in a columnar fashion, as evidenced by small- and wide-angle X-ray scattering. Photoexcitation of these supramolecular assemblies results in rapid formation of DAB(+center dot)-PDI-center dot spin-polarized radical ion pairs having spin-spin dipolar interactions, which show that the average distance between the two radical ions is much larger in the assemblies (31 angstrom) than it is in their monomeric building blocks (23 angstrom). This work demonstrates that electron hopping through the pi-stacked PDI molecules is fast enough to compete effectively with charge recombination (40 ns) in these systems, making these materials of interest as photoactive assemblies for artificial photosynthesis and organic photovoltaics.
引用
收藏
页码:11919 / 11929
页数:11
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