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Dynamic Covalent Formation of Concave Disulfide Macrocycles Mechanically Interlocked with Single‐Walled Carbon Nanotubes

The formation of discrete macrocycles wrapped around single‐walled carbon nanotubes (SWCNTs) has recently emerged as an appealing strategy to functionalize these carbon nanomaterials and modify their properties. Here, we demonstrate that the reversible disulfide exchange reaction, which proceeds und...

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Detalles Bibliográficos
Autores principales: Balakrishna, Bugga, Menon, Arjun, Cao, Kecheng, Gsänger, Sebastian, Beil, Sebastian B., Villalva, Julia, Shyshov, Oleksandr, Martin, Oliver, Hirsch, Andreas, Meyer, Bernd, Kaiser, Ute, Guldi, Dirk M., von Delius, Max
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590186/
https://www.ncbi.nlm.nih.gov/pubmed/32544289
http://dx.doi.org/10.1002/anie.202005081
Descripción
Sumario:The formation of discrete macrocycles wrapped around single‐walled carbon nanotubes (SWCNTs) has recently emerged as an appealing strategy to functionalize these carbon nanomaterials and modify their properties. Here, we demonstrate that the reversible disulfide exchange reaction, which proceeds under mild conditions, can install relatively large amounts of mechanically interlocked disulfide macrocycles on the one‐dimensional nanotubes. Size‐selective functionalization of a mixture of SWCNTs of different diameters were observed, presumably arising from error correction and the presence of relatively rigid, curved π‐systems in the key building blocks. A combination of UV/Vis/NIR, Raman, photoluminescence excitation, and transient absorption spectroscopy indicated that the small (6,4)‐SWCNTs were predominantly functionalized by the small macrocycles 1(2), whereas the larger (6,5)‐SWCNTs were an ideal match for the larger macrocycles 2(2). This size selectivity, which was rationalized computationally, could prove useful for the purification of nanotube mixtures, since the disulfide macrocycles can be removed quantitatively under mild reductive conditions.