Discovery of an Interlocked and Interwoven Molecular Topology in Nanocarbons via Dynamic C–C Bond Formation

Topologically complex carbon nanostructures are an exciting but largely unexplored class of materials due to their challenging synthesis. Previous methods are low yielding because they rely on irreversible C<sub>sp<sup>2</sup></sub>-C<sub>sp<sup>2</sup></sub> bond formation, which necessitates complex templating strategies to enforce entanglement. Here, reversible zirconocene coupling of alkynes is developed as a new method to access complex molecular topologies, where dynamic C-C bond formation facilitates entanglement under thermodynamic control, allowing the use of simple precursors without the need for preassembly. This strategy enables the scalable, high-yield synthesis of three topologically distinct nanocarbons, including the serendipitous discovery of a structure containing a new topological motif that was not previously identified or realized synthetically. This motif, consisting of an unusual combination of interlocking and interweaving, was recognized to be generalizable to a new topological class of molecules, introduced here as perplexanes.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-05-23
DOI
https://doi.org/10.1021/jacs.5c04268
Citations
9
Primary Topic
Supramolecular Chemistry and Complexes
Type
article
Field-Weighted Citation Impact
8.42

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article

Discovery of an Interlocked and Interwoven Molecular Topology in Nanocarbons via Dynamic C–C Bond Formation

Harrison M. Bergman, Angela Fan, August J. Rothenberger, Hosea M. Nelson et al.
9 citations
Journal of the American Chemical Society
Supramolecular Chemistry and Complexes
8.42
article

Discovery of an Interlocked and Interwoven Molecular Topology in Nanocarbons via Dynamic C–C Bond Formation

Harrison M. Bergman, Angela Fan, August J. Rothenberger, Hosea M. Nelson, Kunal Kumar Jha, T. Don Tilley, Rex C. Handford, Yi Liu, Christopher G. Jones
article en
9 citations

Abstract

Topologically complex carbon nanostructures are an exciting but largely unexplored class of materials due to their challenging synthesis. Previous methods are low yielding because they rely on irreversible C<sub>sp<sup>2</sup></sub>-C<sub>sp<sup>2</sup></sub> bond formation, which necessitates complex templating strategies to enforce entanglement. Here, reversible zirconocene coupling of alkynes is developed as a new method to access complex molecular topologies, where dynamic C-C bond formation facilitates entanglement under thermodynamic control, allowing the use of simple precursors without the need for preassembly. This strategy enables the scalable, high-yield synthesis of three topologically distinct nanocarbons, including the serendipitous discovery of a structure containing a new topological motif that was not previously identified or realized synthetically. This motif, consisting of an unusual combination of interlocking and interweaving, was recognized to be generalizable to a new topological class of molecules, introduced here as perplexanes.

Journal of the American Chemical SocietyVol. 147(22)
California Institute of Technology (US), Lawrence Berkeley National Laboratory (US), University of California, Los Angeles (US), University of California System (US), Division of Chemistry (US), Foundry (United Kingdom) (GB), Molecular Foundry, University of California, Berkeley (US)
Division of Chemistry, Basic Energy Sciences
Openalex Percentile: Top 2%
Supramolecular Chemistry and Complexes
8.42
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