journal article·2024-01Open access

Synthesis of linear [7]- and [8]catenanes

Gray H. Harlan, Sheila L. Tran, Nathan D. Colley, Mark A. Nosiglia, Yipei Zhang, Jonathan C. Barnes

Cell Reports Physical Science· Volume 5· Issue 1

Abstract

Catenanes are a family of mechanically interlocked molecules that consist of molecular rings that can be interlocked to give linear, radial, or cyclic structures. Although chemists have pursued extended linear poly[n]catenane architectures for many decades, there still exists a fundamental gap between the synthesis of well-defined, linear oligomers and that of disperse polymers that are often produced as a mixture of architectures. Here, we report two convergent one-pot syntheses that “zip-tie” together two pre-made [3]catenanes by first using orthogonal metal templation with phenanthroline (Cu(I)) and terpyridine (Fe(II)) ligands. These pre-catenate complexes were subjected to a ring-closing metathesis step to afford discrete, linear [7]- and [8]catenanes. The successful synthesis and isolation of the discrete [7]- and [8]catenanes were confirmed using multiple methods of characterization. Because these record-setting linear [n]catenanes possess open phenanthroline metal-binding sites at each end, further expansion to all-interlocked linear poly[n]catenanes is a realistic proposition.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Supramolecular Chemistry and Complexes · Chemical Synthesis and Analysis · Molecular Sensors and Ion Detection

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (32)

Show source-provided references
1. Mechanically Interlocked Molecules (MIMs)—Molecular Shuttles, Switches, and Machines (Nobel Lecture)10.1002/anie.201703216 ↗
2. The chemistry of the mechanical bond10.1039/b819333a ↗
3. Development of pseudorotaxanes and rotaxanes: from synthesis to stimuli-responsive motions to applications10.1021/cr5005869 ↗
4. Catenanes: fifty years of molecular links10.1002/anie.201411619 ↗
5. Bistable [c2] Daisy Chain Rotaxanes as Reversible Muscle-like Actuators in Mechanically Active Gels10.1021/jacs.7b06710 ↗
6. Fast response dry-type artificial molecular muscles with [c2]daisy chains10.1038/nchem.2513 ↗
7. Highly Stretchable and Instantly Recoverable Slide-Ring Gels Consisting of Enzymatically Synthesized Polyrotaxane with Low Host Coverage10.1021/acs.chemmater.8b01208 ↗
8. Crack propagation resistance of slide-ring gels10.1016/j.polymer.2019.121782 ↗
9. Distinctive features and challenges in catenane chemistry10.1039/D1SC05391D ↗
10. Mechanically interlocked materials. Rotaxanes and catenanes beyond the small molecule10.1039/C8CS00888D ↗
11. Unexpected Synthesis of an 8-Shaped Macrocycle Instead of an Interlocking-Ring System10.1021/ic991502k ↗
12. Amabilino · Angew. Chem. Int. Ed. Engl. · 1994 · 33 · 128610.1002/anie.199412861 ↗
13. Template-directed synthesis of donor/acceptor [2] catenanes and [2] rotaxanes10.1351/pac200880030485 ↗
14. Oligocatenanes Made to Order110.1021/ja9720873 ↗
15. Synthesis of linear [5] catenanes via olefin metathesis dimerization of pseudorotaxanes composed of a [2] catenane and a secondary ammonium salt10.1039/C5CC07562A ↗
16. Catenane crosslinked mechanically adaptive polymer gel10.1002/marc.201700361 ↗
17. Anion templated assembly of mechanically interlocked structures10.1039/B518077P ↗
18. Metal ions in the synthesis of interlocked molecules and materials10.1039/C7CS00199A ↗
19. Synthesis of Catenane Structures via Ring-Closing Metathesis10.1021/jo990268c ↗
20. Topologically Controlled Syntheses of Unimolecular Oligo[n]catenanes10.1021/acscentsci.2c00697 ↗
21. Effect of metallosupramolecular polymer concentration on the synthesis of poly [n] catenanes10.1039/D1SC02450G ↗
22. Poly[n]catenanes: Synthesis of molecular interlocked chains10.1126/science.aap7675 ↗
23. Construction of interlocking and threaded rings using two different transition metals as templating and connecting centers: Catenanes and rotaxanes incorporating Ru (terpy) 2-units in their framework10.1021/ja963955j ↗
24. One-Pot Synthesis of a Linear [4]Catenate Using Orthogonal Metal Templation and Ring-Closing Metathesis10.1021/acs.inorgchem.0c00735 ↗
25. Macrocycle Dynamics in a Branched [8]Catenane Controlled by Three Different Stimuli in Three Different Regions10.1002/anie.202110200 ↗
26. Metalation/Demetalation as a Postgelation Strategy To Tune the Mechanical Properties of Catenane-Crosslinked Gels10.1021/jacs.2c03166 ↗
27. Ring-Opening Metathesis Polymerization of a Diolefinic [2]-Catenane–Copper(I) Complex: An Easy Route to Polycatenanes10.1021/ma502392v ↗
28. Magic Ring Catenation by Olefin Metathesis10.1021/ol050463f ↗
29. Selecting topology and connectivity through metal-directed macrocyclization reactions: a square planar palladium [2] catenate and two noninterlocked isomers10.1021/ja053005a ↗
30. Synthesis of achiral and racemic catenanes based on terpyridine and a directionalized terpyridine mimic, pyridyl-phenanthroline10.1039/b506101f ↗
31. Getting harder: cobalt (III)-template synthesis of catenanes and rotaxanes10.1021/ja809627j ↗
32. Control over the macrocyclisation pathway and product topology in a copper-templated catenane synthesis10.1039/C9CC02263E ↗