Synthetic access to calix[3]pyrroles via meso-expansion: hosts with diverse guest chemistry

Calix[3]pyrroles were synthesized for the first time. These macrocycles display versatile guest binding ability based on the bridges connecting the two α-positions of the tripyrrane moiety e.g. with an ethene bridge they showed colorimetric sensing of fluoride and cyanide ions, whereas with a phenyl...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2020-05, Vol.56 (42), p.5637-5640
Hauptverfasser: Sathish Kumar, B, Pati, Narendra N, Jose, K V Jovan, Panda, Pradeepta K
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Sprache:eng
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Zusammenfassung:Calix[3]pyrroles were synthesized for the first time. These macrocycles display versatile guest binding ability based on the bridges connecting the two α-positions of the tripyrrane moiety e.g. with an ethene bridge they showed colorimetric sensing of fluoride and cyanide ions, whereas with a phenylene spacer they exhibited fluorometric sensing of fluoride ions only, and the macrocycle with an ethylene unit acted as a host towards the water molecule with unique penta-coordinated oxygen in the solid state.
ISSN:1359-7345
1364-548X
DOI:10.1039/d0cc01447h