6533b870fe1ef96bd12cfba8
RESEARCH PRODUCT
N ‐Annulated Perylene Bisimides to Bias the Differentiation of Metastable Supramolecular Assemblies into J‐ and H‐Aggregates
Enrique OrtíElisa E. GrecianoJoaquín CalboLuis Sánchezsubject
chemistry.chemical_classification010405 organic chemistryChemistrySupramolecular chemistryGeneral ChemistryPolymerGeneral Medicine010402 general chemistryElectrostatics01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographysymbols.namesakeMetastabilityAmidesymbolsvan der Waals forceJ-aggregatePerylenedescription
The unique self-assembling features of N-annulated perylene bisimides (PBIs) 1 and 2 are reported. The stability of the aggregates of diester 1, in which no H-bonding interactions are operative, corroborates the significance of long-range van der Waals and dipole-dipole electrostatic interactions in the construction of stable supramolecular assemblies. The incorporation of amide functional groups within the N-annulated PBI in 2 stimulates pathway differentiation to achieve up to three J-type aggregates and a fourth H-type aggregate depending on the experimental conditions. The results presented demonstrate unprecedented levels of control over synthetic supramolecular self-assembly and the rich differentiation that N-annulated PBIs exhibit, opening the door to new, complex, functional supramolecular materials.
year | journal | country | edition | language |
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2020-07-14 | Angewandte Chemie |