Perylene Diimide: Versatile Building Blocks for Molecular Self-Assemblies, Folding Motifs, and Reaction-Directing Codes

被引:50
作者
Zhan, Chuanglang [2 ]
Li, Alexander D. Q. [1 ]
机构
[1] Washington State Univ, Dept Chem, Pullman, WA 99164 USA
[2] Chinese Acad Sci, Inst Chem, Lab Photochem, BNLMS, Beijing 100190, Peoples R China
基金
美国国家科学基金会;
关键词
Perylene; self-assembly; folding; Franck-Condon; fluorescence; CHANNEL ORGANIC SEMICONDUCTORS; CHARGE-TRANSPORT; ELECTROCHEMICAL PROPERTIES; ELECTRON-TRANSFER; CRYSTAL-STRUCTURE; ENERGY-TRANSFER; PHOTOSYSTEM-II; BISIMIDE DYES; PI-STACKS; FLUORESCENT;
D O I
10.2174/138527211795378182
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Perylene diimides (PDIs) have been playing important roles in several active fields. Therefore, we will first review the current methods to modify the skeleton of perylene diimides. Next, PDI self-assemblies and PDI folded nanostructures and chemically restrained PDI nanostructures are presented. Unusual physical properties due to nanostructures formation are discussed including the absorption band intensity reversal and pi-stack red-fluorescence emission. Because of interesting pi-stacked structures, PDI derivatives are considered as potential candidates for photovoltaic applications and organic electronics. More importantly, pi-stacking can be tuned when the dihedral angle of the two naphthalene planes varies, thus resulting in adjusted interacting forces. Such cooperative forces lead to the discovery of molecular code phenomena, which will have profound impact an future bi-molecular reaction designs.
引用
收藏
页码:1314 / 1339
页数:26
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