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Rotaxanes and Catenanes by Click Chemistry

机译:点击化学的轮烷和链烷

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Copper(I)-catalyzed Huisgen 1,3-dipolar cycloaddition between terminal alkynes and azides - also known as the copper (Cu)-catalyzed Azide-Alkyne Cycloaddition (CuAAC) - has been used in the syntheses of molecular compounds with diverse structures and functions, owing to its functional group tolerance, facile execution, and mild reaction conditions under which it can be promoted. Recently, rotaxanes of four different structural types, as well as donor/acceptor catenanes, have been prepared using CuAAC, attesting to its tolerance to supramolecular interactions as well. In one instance of a rotaxane synthesis, the catalytic role of copper has been combined successfully with its previously documented ability to preorganize rotaxane precursors, i.e., form pseudoro-taxanes. The crystal structure of a donor/acceptor catenane formed using the CuAAC reaction indicates that any secondary [pi...pi] interactions between the 1,2,3-triazole ring and the bipyridinium pi-acceptor are certainly not destabilizing. Finally, the preparation of robust rotaxane and catenane molecular monolayers onto metal and semiconductor surfaces is premeditated based upon recent advances in the use of the Huisgen reaction for surface functionalization.
机译:末端炔烃与叠氮化物之间的铜(I)催化的惠斯根1,3-偶极环加成反应-也称为铜(Cu)催化的叠氮化物-炔烃环加成反应(CuAAC)-已用于合成具有不同结构和结构的分子化合物由于其功能基团的耐受性,执行的简便性和在温和的反应条件下可以促进它的功能,因此可以发挥作用。最近,使用CuAAC制备了四种不同结构类型的轮烷,以及供体/受体链烷,也证明了其对超分子相互作用的耐受性。在轮烷的合成的一种情况下,铜的催化作用已经与先前记录的将轮烷前体预组织,即形成假轮烷的能力成功地结合在一起。使用CuAAC反应形成的供体/受体链烷的晶体结构表明,1,2,3-三唑环和联吡啶鎓pi-受体之间的任何次级π相互作用当然不会使不稳定。最后,基于在使用惠斯根反应进行表面功能化方面的最新进展,对在金属和半导体表面上制备坚固的轮烷和链烷分子单分子层的方法进行了预谋。

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