One-Pot Synthesisof Tridentate BicyclocalixareneCage Molecules

Efficient one-pot synthesis of tridentate bicyclocalixarenes was developed by condensing phloroglucinol with dechlorinated pyrimidine or triazine with a yield up to 58%. These cage-like molecules adopt a symmetric three-blade propeller structure with different terminal function groups and arm spans ranging from 7.5 to 15.8 Å. Due to the 1,3-alternate configuration of intermediate heterocalixarenes, the cage molecules can be prepared only with benzene rings as the upper and lower caps. They will be an ideal scaffold for the preparation of ultrathin two-dimensional materials.

Publication Details

Journal
Figshare
Published
2025-02-19
DOI
https://doi.org/10.1021/acs.orglett.5c00037.s001
Primary Topic
Supramolecular Chemistry and Complexes
Type
article
Field-Weighted Citation Impact
0.00
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article

One-Pot Synthesisof Tridentate BicyclocalixareneCage Molecules

Figshare
Supramolecular Chemistry and Complexes
article

One-Pot Synthesisof Tridentate BicyclocalixareneCage Molecules

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Abstract

Efficient one-pot synthesis of tridentate bicyclocalixarenes was developed by condensing phloroglucinol with dechlorinated pyrimidine or triazine with a yield up to 58%. These cage-like molecules adopt a symmetric three-blade propeller structure with different terminal function groups and arm spans ranging from 7.5 to 15.8 Å. Due to the 1,3-alternate configuration of intermediate heterocalixarenes, the cage molecules can be prepared only with benzene rings as the upper and lower caps. They will be an ideal scaffold for the preparation of ultrathin two-dimensional materials.

Figshare
Openalex Percentile: Top 58%
Supramolecular Chemistry and Complexes
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One-Pot Synthesisof Tridentate BicyclocalixareneCage Molecules · Figshare (2025) | TGRS Research Map | TGRS