Anion recognition by diureido-calix[4]arenes in the 1,3-alternate conformation

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F09%3A00021455" target="_blank" >RIV/60461373:22310/09:00021455 - isvavai.cz</a>

Alternative codes found

RIV/61388980:_____/09:00332779 RIV/67985858:_____/09:00332779

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Anion recognition by diureido-calix[4]arenes in the 1,3-alternate conformation

Original language description

A series of diureido-calix[4]arenes immobilised in the 1,3-alternate conformation was synthesised and systematically studied for their complexation ability. As revealed by H-1 NMR and UV/vis titrations, this structural motif leads to very efficient ligands for anion recognition with high binding constants in nonpolar solvents. The comparison with the corresponding ligands possessing the cone conformation indicates that diureido-calix[4]arene in a 1,3-alternate conformation are very promising anion receptors with pronounced binding ability towards carboxylates.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

Result was created during the realization of more than one project. More information in the Projects tab.

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year

2009

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

New Journal of Chemistry

ISSN

1144-0546

e-ISSN

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Volume of the periodical

33

Issue of the periodical within the volume

3

Country of publishing house

GB - UNITED KINGDOM

Number of pages

8

Pages from-to

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UT code for WoS article

000263922500022

EID of the result in the Scopus database

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