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

Author(s): Chuanglang Zhan, Alexander D. Q. Li.

Journal Name: Current Organic Chemistry

Volume 15 , Issue 9 , 2011

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Abstract:

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 π-stack red-fluorescence emission. Because of interesting π-stacked structures, PDI derivatives are considered as potential candidates for photovoltaic applications and organic electronics. More importantly, π-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.

Keywords: Perylene, self-assembly, folding, Franck-Condon, fluorescence, PDI aromatic core, dibenzocoronene tetracarboxydiimide, nitrogen-fused heterocoronene tetracarboxydiimide, palladium-catalyzed dehydrohalogenation, PDI-DNA Conjugates, Duplex Formation, Hairpin Formation, organic thin-film transistors, photochromic spiropyran, photoswitchable nanoprobes, electron nuclear double resonance (ENDOR)

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Article Details

VOLUME: 15
ISSUE: 9
Year: 2011
Page: [1314 - 1339]
Pages: 26
DOI: 10.2174/138527211795378182
Price: $58

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