Computational and experimental studies of di- and tetrasubstituted calix[4]arenes

✍ Scribed by Harold D. Banks; Alessandro Dondoni; Martin Kleban; Alberto Marra

• Publisher: John Wiley and Sons
• Year: 2002
• Tongue: English
• Weight: 102 KB
• Volume: 14
• Category: Article
• ISSN: 0899-0042
• DOI: 10.1002/chir.10059

✦ Synopsis

Abstract

Calixarenes are molecular bowls or baskets that have been demonstrated to serve as hosts for cations, anions, and neutral molecules. The central cavity and scaffolding of various functionalities on the upper and lower rims establishes this class of compounds as extremely important in supramolecular chemistry studies. In earlier studies, calixsugars (molecules that have sugar molecules appended to the upper rim of the calix) were prepared. Among the potential advantages of these molecules are increased water solubility and enhanced possibilities that these chiral attachments can promote enantiomeric selection. Computational studies, however, have indicated that the chosen calixsugars had significantly encumbered upper rims, suggesting that host–guest associations would be limited. In an attempt to understand those factors responsible for the favored conformations of calixsugars, a number of 5,17‐disubstituted and tetrasubstituted calix[4]arenes were prepared and studied experimentally as well as by molecular mechanics conformational searching techniques. Chirality 14:173–179, 2002. Published 2002 Wiley‐Liss, Inc.