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DOI: 10.1055/s-0042-1751947
Topologically Chiral Nanohoops
Lemniscular Carbon Nanohoops with Contiguous Conjugation from Planar Chiral [2.2]Paracyclophane: Influence of the Regioselective Synthesis on Topological Chirality.
Chem. Sci. 2023;
14: 4426-4433
Significance
As a novel chiral element, topological chirality has expanded the research and application horizon of related functional materials. While synthetic strategies for the non-conjugated counterparts have been widely investigated, methods for conjugated structures of topological chirality are relatively less explored. Herein, two isomeric nanohoops of conjugated backbone are constructed by harnessing [2.2]paracyclophane as the hinge unit.
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Comment
Introducing different silyl protective groups regiospecifically to the central chiral paracyclophane is crucial to the subsequent site-specific ring closure and achievement of the topological chirality. The inherent difference in the structural topology exhibited by the two isomers results in their distinct chiral traits and chiroptical properties.
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Publication History
Article published online:
14 July 2023
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