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Discrete pi-Stacks from Self-Assembled Perylenediimide Analogues
- Source :
- Angewandte Chemie. International Edition, 131, 15417-15421, Angewandte Chemie-International Edition, 58(43), 15273-15277. Wiley, Angewandte Chemie. International Edition, 131, pp. 15417-15421
- Publication Year :
- 2019
-
Abstract
- The formation of well-defined finite-sized aggregates represents an attractive goal in supramolecular chemistry. In particular, construction of discrete π-stacked dye assemblies remains a challenge. Reported here is the design and synthesis of a novel type of discrete π-stacked aggregate from two comparable perylenediimide (PDI) dyads (PEP and PBP). The criss-cross PEP-PBP dimers in solution and (PBP-PEP)-(PEP-PBP) tetramers in the solid state are well elucidated using single-crystal X-ray diffraction, dynamic light scattering, and diffusion-ordered NMR spectroscopy. Extensive π–π stacking between the PDI units of PEP and PBP as well as repulsive interactions of swallow-tailed alkyl substituents are responsible for the selective formation of discrete dimer and tetramer stacks. Our results reveal a new approach to preparing discrete π stacks that are appealing for making assemblies with well-defined optoelectronic properties.
- Subjects :
- Materials science
Dimer
education
Stacking
Supramolecular chemistry
chirality
Nanotechnology
010402 general chemistry
01 natural sciences
Catalysis
Self assembled
chemistry.chemical_compound
noncovalent interactions
Tetramer
Non-covalent interactions
Alkyl
chemistry.chemical_classification
010405 organic chemistry
structure elucidation
General Medicine
General Chemistry
Nuclear magnetic resonance spectroscopy
self-assembly
0104 chemical sciences
Crystallography
chemistry
bacteria
Self-assembly
Physical Organic Chemistry
supramolecular structures
Subjects
Details
- ISSN :
- 14337851
- Database :
- OpenAIRE
- Journal :
- Angewandte Chemie. International Edition, 131, 15417-15421, Angewandte Chemie-International Edition, 58(43), 15273-15277. Wiley, Angewandte Chemie. International Edition, 131, pp. 15417-15421
- Accession number :
- edsair.doi.dedup.....5c3a3830f241f15581eba590967c0240