Journal
MACROHETEROCYCLES
Volume 7, Issue 4, Pages 345-350Publisher
IVANOVO STATE UNIV CHEMICAL TECHNOLOGY
DOI: 10.6060/mhc140720s
Keywords
Thiacalix[4]arenes; synthesis; molecular recognition; dicarboxylic acid
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Funding
- Kazan Federal University
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New tetrasubstituted p-tert-butylthiacalix[4]arenes containing 2-, 3-, and 4-picolylamine fragments at the lower rim in 1,3-alternate conformation were synthesized. It was shown that the macrocycles synthesized are able to bind selectively phthalic acid in the series of dicarboxylic (oxalic, malonic, succinic, adipic, glutaric, fumaric, maleic, isophthalic and terephthalic) and hydroxy (glycolic and tartaric) acids.
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