CLATHRATION OF PROPERLY FUNCTIONALIZED CALIX[4]ARENES - C-13 CP-MAS NMR-SPECTROSCOPY AND X-RAY CRYSTALLOGRAPHY

Citation
W. Verboom et al., CLATHRATION OF PROPERLY FUNCTIONALIZED CALIX[4]ARENES - C-13 CP-MAS NMR-SPECTROSCOPY AND X-RAY CRYSTALLOGRAPHY, Gazzetta chimica italiana, 127(11), 1997, pp. 727-739
Citations number
27
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Chemistry
Journal title
ISSN journal
0016-5603
Volume
127
Issue
11
Year of publication
1997
Pages
727 - 739
Database
ISI
SICI code
0016-5603(1997)127:11<727:COPFC->2.0.ZU;2-8
Abstract
The clathrate formation of a series of differently upper-rim-functiona lized tetrapropoxycalix[4]arenes has been investigated. In the cases o f 5,17-dinitro-, 3, and 5,17-diphthalimidocalix[4]arene, 5, clathrates were obtained with benzene, toluene, p-xylene, and anisole, and for 3 also with o- and m-xylene, mesitylene, chlorobenzene, and nitrobenzen e. The clathrate formation of 3 with toluene and p-xylene has been stu died with C-13 CP-MAS NMR spectroscopy. In the latter case X-Ray analy sis at 173 K revealed that the p-xylene is located between the calix[4 ]arenes in channels. X-Ray analysis at 173 K and C-13 CP-MAS spectrosc opy of the clathrate of tetra-tert-butylcalix[4]arene, 12, and acetoni trile showed that the guest is located in the cavity of the calix[4]ar ene. In the case of calix[4]arene tetracarbonate, 13, a 1:2 clathrate with acetonitrile was obtained with one guest molecule in- and one out side the cavity.