We report the synthesis of a series of the oxygen-depleted conjugated 5,5'-Bicalix[4]arene compounds bearing various substituents at the terminal positions of the conjugated chain and their fluorescence response to the presence of a cationic -methylpyridinium guest. The complexation of this cation within the bicalixarene cavity results in the fluorescence quenching, with the host molecules bearing electron-donating groups demonstrating a stronger fluorescence response. These results show the importance of the electronic effects on the host-guest complexation within the hydrophobic calixarene scaffolds.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661034 | PMC |
http://dx.doi.org/10.1021/acs.joc.3c01566 | DOI Listing |
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