Hydrogen bonding receptors of tetraamide derivatives derived from thiacalix[4]arene in cone- and 1,3-alternate conformation

Autor:	Mark R. J. Elsegood, Carol Pérez-Casas, Akina Yoshizawa, Takehiko Yamato, Carl Redshaw, Shofiur Rahman
Rok vydání:	2008
Předmět:	Chemistry Hydrogen bond Stereochemistry Intramolecular force Proton NMR Halide Titration General Chemistry Condensed Matter Physics Receptor Single crystal Food Science
Zdroj:	Journal of Inclusion Phenomena and Macrocyclic Chemistry. 63:301-308
ISSN:	1573-1111 0923-0750
DOI:	10.1007/s10847-008-9523-4
Popis:	Novel ditopic receptors of tetraamide derivatives possessing four 2-pyridyl groups derived from thiacalix[4]arene in cone- and 1,3-alternate conformation were prepared. The structure of one of the tetraamide derivatives was confirmed by a single crystal X-ray analysis. The tetrathiacalix[4]arene tetraamides show strong intramolecular hydrogen bonding. The binding behaviour towards Ag+ and halides has been investigated by 1H NMR titration experiments.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::ceb2fd64227ee93d206fe92e7edcccf9 https://doi.org/10.1007/s10847-008-9523-4 Zobrazit plný text záznamu Full text from SpringerLink