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Topologically novel multiple rotaxanes and catenanes based on tetraurea calix[4]arenes.

作者信息

Bogdan Anca, Rudzevich Yuliya, Vysotsky Myroslav O, Böhmer Volker

机构信息

Fachbereich Chemie, Pharmazie und Geowissenschaften, Abteilung Lehramt Chemie, Johannes Gutenberg-Universität, Duesbergweg 10-14, D-55099 Mainz, Germany.

出版信息

Chem Commun (Camb). 2006 Jul 28(28):2941-52. doi: 10.1039/b601699e. Epub 2006 Apr 7.

Abstract

Calix[4]arenes bearing at their wide rim four urea residues easily form hydrogen bonded dimeric capsules. This has been used to preorganise alkenyl functions attached to these urea groups for their controlled connection via metathesis reaction. Multimacrocyclic tetraurea derivatives are thus obtained in excellent yields via heterodimers which are formed exclusively with tetratosylurea derivatives. Heterodimerisation of such bis- and tetraloop tetraureas leads analogously to multicatenanes, or to rotaxanes by stoppering. Huge macrocycles are detached from tetraloop derivatives by cleavage of the urea function.

摘要

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