4.8 Article

Intra- and intermolecular self-assembly of a 20-nm-wide supramolecular hexagonal grid

Journal

NATURE CHEMISTRY
Volume 12, Issue 5, Pages 468-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41557-020-0454-z

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Funding

  1. National Institutes of Health [R01GM128037]
  2. US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  3. Shanghai University
  4. US Department of Energy, Office of Science, Office of Workforce Development for Teachers and Scientists (WDTS) under the Science Undergraduate Laboratory Internship (SULI) programme
  5. University of South Florida Nexus Initiative (UNI) Award
  6. Natural Science Foundation of Guangdong Province, China [2019A1515011358]

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For the past three decades, the coordination-driven self-assembly of three-dimensional structures has undergone rapid progress; however, parallel efforts to create large discrete two-dimensional architectures-as opposed to polymers-have met with limited success. The synthesis of metallo-supramolecular systems with well-defined shapes and sizes in the range of 10-100 nm remains challenging. Here we report the construction of a series of giant supramolecular hexagonal grids, with diameters on the order of 20 nm and molecular weights greater than 65 kDa, through a combination of intra- and intermolecular metal-mediated self-assembly steps. The hexagonal intermediates and the resulting self-assembled grid architectures were imaged at submolecular resolution by scanning tunnelling microscopy. Characterization (including by scanning tunnelling spectroscopy) enabled the unambiguous atomic-scale determination of fourteen hexagonal grid isomers.

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