Abstract
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.
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CITATION STYLE
Stawski, W., Van Raden, J. M., Patrick, C. W., Horton, P. N., Coles, S. J., & Anderson, H. L. (2023). Strained Porphyrin Tape-Cycloparaphenylene Hybrid Nanorings. Organic Letters, 25(2), 378–383. https://doi.org/10.1021/acs.orglett.2c04089
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