Crystal transformation from the incorporation of coordinate bonds into a hydrogen-bonded network yields robust free-standing supramolecular membranes

, , , , , , , & (2020) Crystal transformation from the incorporation of coordinate bonds into a hydrogen-bonded network yields robust free-standing supramolecular membranes. Journal of the American Chemical Society, 142(1), pp. 479-486.

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Description

In this work, we report on the synthesis of a free-standing, macroscopic robust supramolecular membrane by introducing silver-nitrogen coordinate bonding into preorganized, supramolecular hydrogen-bonded cyanuric acid-melamine (CAM) crystals. With the assistance of ammonia, silver ions competitively replace two of the three hydrogen atoms from cyanuric acid resulting in the transformation from short CAM nanorods to long CAM-Ag nanofibers (length over 1000 μm), accompanied by tautomerization of cyanuric acid. The single crystal structure of the CAM-Ag nanofibers is solved in the space group P1, with the asymmetric unit containing eight silver atoms, four melamine and four cyanuric acid molecules, which generate 1D coordination polymer chains consisting of alternating melamine and dianionic cyanurate ligands linked via silver-nitrogen bonds. The presence of interchain hydrogen bonds results in the expansion of the supramolecular network into undulating 2D sheets, which then stack into a 3D network via a series of intersheet hydrogen bonds and π-πinteractions. Significantly, the CAM-Ag nanofibers spontaneously assemble into a free-standing membrane, with lateral size up to square centimeters and thickness of 30 μm. The membrane shows high flexibility and mechanical strength, owing to the improved flexibility of the CAM-Ag nanofibers with bonded chain structure, and can be reversibly and repeatedly bent over 90 degrees. Remarkably, the CAM-Ag membrane demonstrates distinct optical transmittance being shortwave IR transmissive but impenetrable to UV and visible light.

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38 citations in Scopus
26 citations in Web of Science®
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ID Code: 198829
Item Type: Contribution to Journal (Journal Article)
Refereed: Yes
ORCID iD:
Meng, Pengorcid.org/0000-0002-4624-2430
Yan, Chengorcid.org/0000-0002-4909-439X
McMurtrie, Johnorcid.org/0000-0003-3990-8617
Xu, Jingsanorcid.org/0000-0003-1172-3864
Measurements or Duration: 8 pages
DOI: 10.1021/jacs.9b11336
ISSN: 0002-7863
Pure ID: 57580683
Divisions: Current > Research Centres > Centre for Materials Science
Current > Research Centres > Centre for Biomedical Technologies
Past > Institutes > Institute for Future Environments
Past > QUT Faculties & Divisions > Science & Engineering Faculty
Current > QUT Faculties and Divisions > Faculty of Science
Current > Schools > School of Chemistry & Physics
Current > QUT Faculties and Divisions > Faculty of Engineering
Current > Schools > School of Mechanical, Medical & Process Engineering
Current > Research Centres > Centre for Tropical Crops and Biocommodities
Funding Information: The authors acknowledge the financial support by the Australian Research Council. Science and Engineering Faculty and Central Analytical Research Facility (CARF) at QUT are greatly acknowledged for technical assistance. The single crystal X-ray diffraction pattern was collected on the MX2 beamline at the Australian Synchrotron, part of ANSTO. We thank the Synchrotron for travel funding and the beamline staff for their assistance.
Copyright Owner: 2019 American Chemical Society
Copyright Statement: This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of the American Chemical Society, copyright © American Chemical Society after peer review and technical editing by t he publisher. To access the final edited and published work see https://doi.org/10.1021/jacs.9b11336
Deposited On: 08 Apr 2020 05:01
Last Modified: 03 Aug 2024 03:23