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通过磺酸表面功能化实现可逆的离散型到扩展型金属有机多面体转变

Reversible Discrete-to-Extended Metal-Organic Polyhedra Transformation by Sulfonic Acid Surface Functionalization.

作者信息

Troyano Javier, Horike Satoshi, Furukawa Shuhei

机构信息

Institute for Integrated Cell-Material Sciences (WPI-iCeMS), Kyoto University, iCeMS Research Building, Yoshida, Sakyo-ku, Kyoto 606-8501, Japan.

Inorganic Chemistry Department, Autonomous University of Madrid, Madrid 28049, Spain.

出版信息

J Am Chem Soc. 2022 Oct 26;144(42):19475-19484. doi: 10.1021/jacs.2c07978. Epub 2022 Oct 12.

Abstract

Metal-organic polyhedra (MOPs) are molecular porous units in which desired functionalities can be installed with precise geometrical and compositional control. By combing two complementary chemical moieties, such as sulfonic acid groups and Rh(II)-carboxylate paddlewheel, we synthesized a robust water-soluble cuboctahedral MOP with excellent features in both solution and solid states. Herein, we demonstrate that the superior chemical stability of the Rh unit and the elevated number of functional groups on the surface (24 per cage) result in a porous cage with high solubility and stability in water, including acidic, neutral, and basic pH conditions. We also prove that the sulfonic acid-rich form of the cage can be isolated through postsynthetic acid treatment. This transformation involves an improved gas uptake capacity and the capability to reversibly assemble the cages into a three-dimensional (3D) metal-organic framework (MOF) structure. Likewise, this sulfonic acid functionalization provides both MOP and MOF solids with high proton conductivities (>10 S cm), comparable to previously reported high conducting metal-organic materials. The influence of the MOP-to-MOF processing in the gas adsorption capacity indicates that this structural transformation can provide materials with higher and more controllable porous properties. These results illustrate the high potential of acidic MOPs as more flexible porous building units in terms of processability, structural complexity, and tunability of the properties.

摘要

金属有机多面体(MOPs)是分子多孔单元,在其中可以通过精确的几何和组成控制来引入所需的功能。通过将两个互补的化学部分,如磺酸基团和Rh(II)-羧酸桨轮相结合,我们合成了一种坚固的水溶性立方八面体MOP,其在溶液和固态下均具有优异的特性。在此,我们证明Rh单元的卓越化学稳定性以及表面上功能基团数量的增加(每个笼24个)导致了一种在水(包括酸性、中性和碱性pH条件)中具有高溶解度和稳定性的多孔笼。我们还证明,可以通过合成后酸处理分离出富含磺酸的笼形式。这种转变涉及气体吸收能力的提高以及将笼可逆地组装成三维(3D)金属有机框架(MOF)结构的能力。同样,这种磺酸功能化赋予MOP和MOF固体高质子电导率(>10 S cm),与先前报道的高导电金属有机材料相当。MOP到MOF的转变对气体吸附容量的影响表明,这种结构转变可以为材料提供更高且更可控的多孔性质。这些结果说明了酸性MOPs作为在可加工性、结构复杂性和性质可调性方面更灵活的多孔构建单元的巨大潜力。

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