Cao Yudong, Vysotsky Myroslav O, Böhmer Volker
Fachbereich Chemie, Pharmazie und Geowissenschaften, Abteilung Lehramt Chemie, Johannes Gutenberg-Universität Mainz, Duesbergweg 10-14, D-55099 Mainz, Germany.
J Org Chem. 2006 Apr 28;71(9):3429-34. doi: 10.1021/jo0524369.
[reaction: see text] Calix[4]arenes 4, substituted at the wide rim by four N-tolyl-urethane groups, were synthesized, as well as derivatives 10a,b bearing two or three tolyl-urea groups beside of one or two urethane group(s). In contrast to tetra-tolyl urea 11, the urethane derivatives do not form hydrogen-bonded, dimeric capsules in CDCl3 or benzene-d6, but the dimerization can be induced for the triurea 10b by tetraethylammonium cations as guests. The quantitative formation of heterodimers is observed for all urethanes 4 and 10a,bin benzene-d6 in mixtures with a "tetra-loop" tetraurea 14, while "bisloop" tetraureas 13 require di- or triurea derivatives 10a,b for a clean heterodimerization.
[反应:见正文] 合成了在宽环上被四个N-甲苯基-脲基取代的杯[4]芳烃4,以及在一个或两个脲基之外还带有两个或三个甲苯基脲基的衍生物10a、b。与四甲苯基脲11不同,脲基衍生物在CDCl₃或苯-d₆中不会形成氢键连接的二聚体胶囊,但作为客体的四乙铵阳离子可诱导三脲10b发生二聚化。在与“四环”四脲14的混合物中,在苯-d₆中观察到所有脲基化合物4和10a、b都定量形成异二聚体,而“双环”四脲13需要二脲或三脲衍生物10a、b才能实现完全的异二聚化。