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- W2142246404 abstract "Abstract The four expanded p ‐benziporphyrins A,C‐di‐ p ‐benzi[24]pentaphyrin(1.1.1.1.1), N‐fused A‐ p ‐benzi[24]pentaphyrin, A, D ‐di‐ p ‐benzi[28]hexaphyrin(1.1.1.1.1.1), and A,C‐di‐ p ‐benzi[28]hexaphyrin(1.1.1.1.1.1) were obtained in three‐component Lindsey‐type macrocyclizations. These compounds were explored as macrocyclic ligands and as potential aromaticity switches. A BODIPY‐like difluoroboron complex was obtained from the A,C‐di‐ p ‐benzi[24]pentaphyrin, whereas A,C‐di‐ p ‐benzi[28]hexaphyrin yielded a Möbius‐aromatic Pd II complex containing fused pyrrole and phenylene subunits. Conformational behavior, tautomerism, and acid‐base chemistry of the new macrocycles were characterized by means of NMR spectroscopy and DFT calculations. Free base N‐fused A‐ p ‐benzi[24]pentaphyrin showed temperature‐dependent Hückel–Möbius aromaticity switching, whereas the A,C‐di‐ p ‐benzi[28]hexaphyrin formed a Möbius‐aromatic dication." @default.
- W2142246404 created "2016-06-24" @default.
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- W2142246404 creator A5065105042 @default.
- W2142246404 creator A5079251062 @default.
- W2142246404 date "2014-01-15" @default.
- W2142246404 modified "2023-10-18" @default.
- W2142246404 title "Hückel and Möbius Expanded<i>para</i>-Benziporphyrins: Synthesis and Aromaticity Switching" @default.
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- W2142246404 doi "https://doi.org/10.1002/chem.201303676" @default.
- W2142246404 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24431244" @default.
- W2142246404 hasPublicationYear "2014" @default.
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