Host-guest chemistry of giant molecular shape amphiphiles based on POSS-PDI conjugates

Giant shape amphiphiles (GSA) are giant molecules made with nano-building blocks that have distinct shapes. The incompatible packing behaviors of the nano-building blocks of GSA could create cavities within certain conformers of the GSA, but the host-guest chemistry of GSA has not been explored yet....

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Veröffentlicht in:Nanoscale 2021-02, Vol.13 (7), p.4295-43
Hauptverfasser: Chen, Jia, Lin, Heng-Yi, Ji, Xiaohuan, Zhao, Haoru, Sun, Bin, Wang, Chien-Lung, Zhu, Meifang
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Sprache:eng
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Zusammenfassung:Giant shape amphiphiles (GSA) are giant molecules made with nano-building blocks that have distinct shapes. The incompatible packing behaviors of the nano-building blocks of GSA could create cavities within certain conformers of the GSA, but the host-guest chemistry of GSA has not been explored yet. In this study, POSS-PDI-POSS ( PPP ), which is made by connecting two nano-cubes, isobutyl-polyhedral oligomeric silsesquioxanes (POSS), to a conjugated π-conjugated core, perylene diimide (PDI), is demonstrated as a novel acyclic synthetic host. In its bent conformer, PPP shows a cavity next to its PDI core. Via forming host-guest complexes with π-conjugated guests such as pyrene and perylene, PPP is found to transform from the bent-conformer into the extended-conformer, creating the steric features to accommodate guest molecules. Subsequent thermal annealing of the host-guest complexes removes the π-conjugated guests and restores the bent conformation and photophysical properties of PPP , which verifies that PPP , as a novel acyclic host, is capable of dynamic host-guest assembly. Moreover, the results prove that cavities at the molecular level can be created by connecting nano-building blocks with distinct shapes. This finding may inspire developments in the host-guest chemistry of GSA and nanomaterial innovation. Giant shape amphiphiles (GSA) are giant molecules made with nano-building blocks that have distinct shapes.
ISSN:2040-3364
2040-3372
DOI:10.1039/d0nr08934f