A Modular Approach to Potential Synthetic Receptors with Large Surfaces Based on Crown[n]cavitands
Autor: | Huub Kooijman, Willem Verboom, Irene Higler, Anthony L. Spek, David N. Reinhoudt, Harold Boerrigter |
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Přispěvatelé: | Faculty of Science and Technology, Molecular Nanofabrication |
Rok vydání: | 1998 |
Předmět: |
Chemistry
Stereochemistry Building blocks Sodium Organic Chemistry Calix[4]arenes Cavitand chemistry.chemical_element Aromaticity Alkylation Crown Compounds stomatognathic system Hydrophobic surfaces Synthetic Receptors Polymer chemistry Molecule Modular approach Physical and Theoretical Chemistry Cavitands Crown compounds |
Zdroj: | European journal of organic chemistry, 1998(8), 1597-1607. Wiley-VCH Verlag |
ISSN: | 1099-0690 1434-193X |
DOI: | 10.1002/(sici)1099-0690(199808)1998:8<1597::aid-ejoc1597>3.0.co;2-1 |
Popis: | Crown[n]cavitands were synthesized by alkylation of tetrahydroxycavitands with polyethyleneglycol ditosylates. The bridging of two hydroxy groups at adjacent aromatic rings by a pentaethyleneglycol unit is favored over the bridging of two hydroxy groups at opposite aromatic rings. The presence of a sodium base enhances the formation of the 1,2-crown[n]cavitand and improves the yield. The combination of 1,2-crown[6]cavitands with calix[4]arenes or resorcin[4]arenes resulted in potential receptor molecules with large hydrophobic surfaces. |
Databáze: | OpenAIRE |
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