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Novel crown ethers with pendant, proton-ionizable, chromogenic groups

✍ Scribed by Bronislaw P. Czech; David A. Babb; Anna Czech; Richard A. Bartsch


Book ID
112129178
Publisher
Journal of Heterocyclic Chemistry
Year
1989
Tongue
English
Weight
319 KB
Volume
26
Category
Article
ISSN
0022-152X

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πŸ“œ SIMILAR VOLUMES


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The first 1,3-alternate calix[4]arene-bis(crown-6-ethers) with a proton-ionizable group located in front of one crown ether cavity are synthesized. Compared with an analog that has no proton-ionizable group, the two new ligands possess markedly higher Cs + extraction efficiency.

Synthesis of dibenzo-16-crown-5 compound
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## Abstract Structurally related dibenzo‐16‐crown‐5 lariat ethers with pendant ester and ether groups are prepared. Structural variations within the series of alkyl lariat ether esters include changes in the O‐alkyl group, attachment site and nature of the lipophilic group, and length of the spacer