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Domain-selective thermal decomposition within supramolecular nanoribbons

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sword-2022-05-16T18:35:31.original.xml (130 B)
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Author(s)
Cho, Yukio
•
Christoff-Tempesta, Ty
•
Kim, Dae-Yoon
•
Lamour, Guillaume
•
Ortony, Julia H
Date Issued
2021
Journal
Nature Communications
Publisher
Springer Science and Business Media LLC
Citation
Cho, Yukio, Christoff-Tempesta, Ty, Kim, Dae-Yoon, Lamour, Guillaume and Ortony, Julia H. 2021. "Domain-selective thermal decomposition within supramolecular nanoribbons." Nature Communications, 12 (1).
Version
Final published version
Abstract
AbstractSelf-assembly of small molecules in water provides a powerful route to nanostructures with pristine molecular organization and small dimensions (<10 nm). Such assemblies represent emerging high surface area nanomaterials, customizable for biomedical and energy applications. However, to exploit self-assembly, the constituent molecules must be sufficiently amphiphilic and satisfy prescribed packing criteria, dramatically limiting the range of surface chemistries achievable. Here, we design supramolecular nanoribbons that contain: (1) inert and stable internal domains, and (2) sacrificial surface groups that are thermally labile, and we demonstrate complete thermal decomposition of the nanoribbon surfaces. After heating, the remainder of each constituent molecule is kinetically trapped, nanoribbon morphology and internal organization are maintained, and the nanoribbons are fully hydrophobic. This approach represents a pathway to form nanostructures that circumvent amphiphilicity and packing parameter constraints and generates structures that are not achievable by self-assembly alone, nor top-down approaches, broadening the utility of molecular nanomaterials for new targets.
MIT Department
Massachusetts Institute of Technology. Department of Materials Science and Engineering
Terms of Use
Creative Commons Attribution 4.0 International License
https://creativecommons.org/licenses/by/4.0
Persistent DSpace Link
https://hdl.handle.net/1721.1/142559
DOI of Published Version
https://doi.org/10.1038/S41467-021-27536-6
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