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在溶液和固态中,一种基于五并苯衍生的反式双(冠醚)主体与不同末端官能化的对醌衍生物的络合:一种由钾离子控制的可切换络合过程。

Complexation of a pentiptycene-derived trans-bis(crown ether) host with different terminally functionalized paraquat derivatives in solution and the solid state: a switchable complexation process controlled by potassium ions.

机构信息

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Molecular Recognition and Function, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.

出版信息

Org Biomol Chem. 2013 Dec 21;11(47):8183-90. doi: 10.1039/c3ob41700j. Epub 2013 Oct 3.

Abstract

The complexation behaviour of a pentiptycene-derived bis(crown ether), containing two 24-crown-8 moieties in a trans arrangement, and a series of paraquat derivatives with different terminal functional groups was investigated. It was found that all of the paraquat derivatives could form stable 2 : 1 complexes with the pentiptycene-derived host both in solution and the solid state, where multiple non-covalent interactions between the host and the guests played an important role. Moreover, the binding and release of the guests in the complexes could also be efficiently controlled by the removal and addition of potassium ions.

摘要

研究了一种五并苯衍生的双(冠醚),其中包含两个以反式排列的 24-冠-8 部分,以及一系列具有不同末端官能团的对醌衍生物。发现所有对醌衍生物都可以在溶液中和固态中与五并苯衍生的主体形成稳定的 2:1 配合物,其中主体和客体之间的多种非共价相互作用起着重要作用。此外,通过去除和添加钾离子,可以有效地控制配合物中客体的结合和释放。

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