Wilson Thea M, Tauber Michael J, Wasielewski Michael R
Department of Chemistry and Argonne-Northwestern Solar Energy Research Center, Northwestern University, Evanston, Illinois 60208-3113, USA.
J Am Chem Soc. 2009 Jul 1;131(25):8952-7. doi: 10.1021/ja902258g.
A series of linearly linked perylenediimide (PDI) dimers and trimers were synthesized in which the PDI pi systems are nearly orthogonal. These oligomers and several model compounds were singly reduced, and intramolecular electron hopping between the PDI molecules was probed by electron paramagnetic resonance (EPR) and electron nuclear double resonance (ENDOR) spectroscopy. When the functional groups attached to the ends of the oligomers were chosen to make each PDI molecule electronically equivalent, the single electron hops between the PDI molecules with rates that significantly exceed 10(7) s(-1). Rapid electron hopping between pairs of PDI molecules having orthogonal pi systems is unexpected and may expand the possible design motifs for organic electronic materials based on PDI.
合成了一系列线性连接的苝二酰亚胺(PDI)二聚体和三聚体,其中PDI的π体系几乎相互正交。对这些低聚物和几种模型化合物进行了单还原,并通过电子顺磁共振(EPR)和电子核双共振(ENDOR)光谱研究了PDI分子间的分子内电子跳跃。当选择连接在低聚物末端的官能团以使每个PDI分子在电子上等效时,PDI分子间的单电子跳跃速率显著超过10(7) s(-1)。具有正交π体系的PDI分子对之间的快速电子跳跃是出乎意料的,这可能会扩展基于PDI的有机电子材料的可能设计模式。