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Strained Porphyrin Tape–Cycloparaphenylene Hybrid Nanorings

[Image: see text] V-Shaped porphyrin dimers, with masked p-phenylene bridges, undergo efficient oxidative coupling to form meso–meso linked cyclic porphyrin oligomers. Reductive aromatization unmasks the p-phenylenes, increasing the strain. Oxidation then fuses the porphyrin dimers, providing a nano...

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Detalles Bibliográficos
Autores principales: Stawski, Wojciech, Van Raden, Jeff M., Patrick, Connor W., Horton, Peter N., Coles, Simon J., Anderson, Harry L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9872170/
https://www.ncbi.nlm.nih.gov/pubmed/36626241
http://dx.doi.org/10.1021/acs.orglett.2c04089
Descripción
Sumario:[Image: see text] V-Shaped porphyrin dimers, with masked p-phenylene bridges, undergo efficient oxidative coupling to form meso–meso linked cyclic porphyrin oligomers. Reductive aromatization unmasks the p-phenylenes, increasing the strain. Oxidation then fuses the porphyrin dimers, providing a nanoring with curved walls. The strain in this macrocycle bends the p-phenylene and fused porphyrin dimer units (radii of curvature of 11.4 and 19.0 Å, respectively), but it does not significantly alter the electronic structure of the fused porphyrins.