Arene-Perfluoroarene Force Driven Sublimation-Removable Chiral Coassemblies.
Arene-Perfluoroarene Interaction
Chiral Self-Assembly
Circularly Polarized Luminescence
Sacrificial Template Method
Sublimation
Journal
Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543
Informations de publication
Date de publication:
19 Jun 2023
19 Jun 2023
Historique:
received:
12
04
2023
medline:
12
6
2023
pubmed:
24
4
2023
entrez:
24
04
2023
Statut:
ppublish
Résumé
Multiple constituent coassembly is an emerging strategy to manipulate supramolecular chirality and chiroptical properties such as circularly polarized luminescence (CPL). However, the second or third constituent could not be removed from pristine self-assembly. Here we developed a constitute-removable chiral coassembly using sublimation that could realize coassembly with tunable supramolecular chirality, luminescence and CPL properties. Octafluoronapthalene (OFN) with small sublimation enthalpy formed coassemblies with perylene-conjugated peptoids via arene-perfluoroarene (AP) interaction that induced the emergence of macroscopic chirality and hypsochromic luminescence from yellow to green. Coassembly with OFN accelerated one-dimensional growth and induced the emergence of macroscopic chirality and CPL. Despite the stability at ambient conditions, vacuum-treatment triggered fast sublimation of OFN, which behaved as a sacrificial template. Physical removal of OFN retained the helical nanoarchitectures as well as the basic features of Cotton effects and CPL activities. X-ray diffraction suggested the back-fill consolidation occurred on the molecular voids by OFN removal that slightly varied the templated molecular arrangements. Sublimation of perfluorinated building units is green and efficient and non-destructive, which is potentially applicable in constructing template-directed chiroptical materials and devices.
Identifiants
pubmed: 37092858
doi: 10.1002/anie.202305135
doi:
Substances chimiques
Peptoids
0
Perylene
5QD5427UN7
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e202305135Subventions
Organisme : National Natural Science Foundation of China
ID : 21901145, 22171165
Informations de copyright
© 2023 Wiley-VCH GmbH.
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