Experimental Evidence for Unusual Protonation of Tetraethyl p-tert-Butylcalix[4]arene Tetraacetate and the Most Probable Structure of the Resulting Complex-Reference-Cited by-同舟云学术

Experimental Evidence for Unusual Protonation of Tetraethyl p-tert-Butylcalix[4]arene Tetraacetate and the Most Probable Structure of the Resulting Complex

Published:2008-06-01 Issue:4 Volume:20 Page:387-395
ISSN:1061-0278
Container-title:Supramolecular Chemistry
language:en
Short-container-title:Supramolecular Chemistry

Author:

KŘÍŽ Jaroslav¹,Dybal JiŘÍ¹,MakrlÍk Emanuel²,VaŇura Petr³

Affiliation:

1. a Institute of Macromolecular Chemistry, Academy of Sciences of the Czech Republic , Heyrovského sq. 2, 162 06, Prague, Czech Republic

2. b Faculty of Applied Sciences, University of West Bohemia , Husova 11, 306 14, Pilsen, Czech Republic

3. c Prague Institute of Chemical Technology , Technická 5, 166 28, Prague, Czech Republic

Publisher

Informa UK Limited

Subject

General Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10610270701278251

Reference32 articles.

1. Filling the baskets: Complex formation with calixarenes

2. Calixarenes, Macrocycles with(Almost) Unlimited Possibilities

3. The preparation and properties of a new lipophilic sodium selective ether ester ligand derived from p-t-butylcalix[4]arene

4. p-t-Butylcalix[4]arene tetra-acetamide: a new strong receptor for alkali cations [1]

5. Synthesis, x-ray crystal structures, and cation-binding properties of alkyl calixaryl esters and ketones, a new family of macrocyclic molecular receptors

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