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在金属大环框架的孔表面上同时排列多达三种不同的分子:合作与竞争。

Simultaneous arrangement of up to three different molecules on the pore surface of a metal-macrocycle framework: cooperation and competition.

机构信息

Department of Chemistry, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan).

出版信息

Angew Chem Int Ed Engl. 2014 Aug 4;53(32):8310-5. doi: 10.1002/anie.201404179. Epub 2014 May 30.

Abstract

Porous crystals are excellent materials with potential spatial functions through molecular encapsulation within the pores. Co-encapsulation of multiple different molecules further expands their usability and designability. Herein we report the simultaneous arrangement of up to three different guest molecules, TTF (tetrathiafulvalene), ferrocene, and fluorene, on the pore surfaces of a porous crystalline metal-macrocycle framework (MMF). The position and orientation of adsorbed molecules arranged in the pore were determined by single-crystal X-ray diffraction analysis. The anchoring effect of hydrogen bonds between the hydroxy groups of the guest molecules and inter-guest cooperation and competition are significant factors in the adsorption behaviors of the guest molecules. This finding would serve as a design basis of multicomponent functionalized nanospaces for elaborate reactions that are realized in enzymes.

摘要

多孔晶体是一种优秀的材料,通过分子在孔内的封装具有潜在的空间功能。多种不同分子的共封装进一步扩展了它们的可用性和可设计性。在此,我们报告了多达三种不同客体分子(TTF(四硫富瓦烯)、二茂铁和芴)在多孔晶体金属大环骨架(MMF)的孔表面上的同时排列。通过单晶 X 射线衍射分析确定了吸附在孔中的分子的位置和取向。客体分子的羟基之间氢键的锚固效应以及客体之间的合作和竞争是客体分子吸附行为的重要因素。这一发现将为在酶中实现的精细反应的多功能功能化纳米空间的设计提供基础。

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