Abstract:Calixareneglycine ester acetamides 4a–c have been synthesized from calixareneacetyl chlorides 5a–c and glycine ethyl ester (6). Their ion‐binding properties have been investigated by liquid‐liquid extraction with radiotracer techniques. The experiments reveal a moderate affinity towards silver(I) ions, which increases with calixarene ring size.
“…Literature procedures were used for synthesis of compounds 2 [15], 3 [16], 4 [17], 8 [18], 9-11 [19], 12 and 13 [20], 14 [21], 16 [22], and 24 [23].…”
Competitive carrier-mediated co-extraction and co-transport of a variety of anions and their counter ions into an organic phase or through supported liquid hydrophobic membranes from aqueous mixtures of salts have been monitored by ion chromatography. The method enables rapid screening of the anion co-transport or co-extraction ability of new potential ionophores and carrier molecules.
“…Literature procedures were used for synthesis of compounds 2 [15], 3 [16], 4 [17], 8 [18], 9-11 [19], 12 and 13 [20], 14 [21], 16 [22], and 24 [23].…”
Competitive carrier-mediated co-extraction and co-transport of a variety of anions and their counter ions into an organic phase or through supported liquid hydrophobic membranes from aqueous mixtures of salts have been monitored by ion chromatography. The method enables rapid screening of the anion co-transport or co-extraction ability of new potential ionophores and carrier molecules.
The recognition abilities of chiral calixarene hosts toward alkali cation guests have been exploited for the first time in asymmetric phase‐transfer catalysis. The binding affinities of a series of chiral α‐methylbenzylamine‐derived calix[4]arene‐amides toward Na+ guest have been determined by 1H NMR spectroscopic titration experiments. The good apparent association constant values are consistent with the macrocycles' catalytic efficiency in the asymmetric alkylation reaction of N‐(diphenylmethylene)glycine esters under phase‐transfer conditions.
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