New p-tert-butyl thiacalix[4]arene derivatives containing simultaneously the 4-amidoazobenzene and ethoxycarbonyl fragments at the lower rim in cone and
It was shown that the chemo-and stereoselective alkylation of the lower rim 1,3-disubstituted p-tert-butyl thiacalix [4] arenes in the cone conformation using 2-chloro-N,N-
Tetracarboxylic acids based on thiacalix[4]arene in 1,3-alternate conformation quench fluorescence of dopamine hydrochloride according to the static mechanism.
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