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

被引:75
作者
Bogdan, Anca [1 ]
Rudzevich, Yuliya [1 ]
Vysotsky, Myroslav O. [1 ]
Boehmer, Volker [1 ]
机构
[1] Univ Mainz, Fachbereich Chem Pharm & Geowissensch, Abt Lehramt Chem, D-55099 Mainz, Germany
关键词
D O I
10.1039/b601699e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:2941 / 2952
页数:12
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