Macrocyclization is a popular method for preparing hosts, but it can have unintended effects, like limiting molecular free rotation to yield mixtures of inseparable isomers. We report a [3 + 3] Schiff-base macrocycle () with anthracene bridges. Restricted rotation about the phenyl-anthracene bonds leads to exist as a mixture of conformations ( and ). Macrocycle was photooxidized to tris(endoperoxide) adduct , alleviating restricted rotation. These results were supported by spectroscopic, structural, and computational analyses.
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http://dx.doi.org/10.1021/acs.orglett.1c03759 | DOI Listing |
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