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Organic Ligands Made Porous: Magnetic and Catalytic Properties of Transition Metals Coordinated to the Surfaces of Mesoporous Organosilica

机译:有机配体制成多孔:过渡金属的介孔有机硅表面配位的磁性和催化性能

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摘要

Inorganic solids with porosity on the mesoscale possess a high internal surface area and a well-accessible pore system. Therefore, it is a relevant task to equip the surfaces of such materials with a maximum density of various organic functional groups. Among these functions it is the capability of coordinating to metal species as a ligand that is of extraordinary importance in many areas, for example, in catalysis. This paper describes how prominent ligands containing donor functions such as carboxylic, thio, chelating, or amine groups can be obtained in the form of nanoporous organosilica materials. The coordination of metal centers such as Co~(II), Mn~(II),V~(IV), or Pt~(IV) is studied in detail. The magnetic properties of the corresponding materials and some applications in catalysis are reported. A quantitative determination of the surface density of donor atoms by distance measurements using EPR spectroscopy is shown.
机译:中孔具有孔隙率的无机固体具有较高的内部表面积和易于使用的孔隙系统。因此,使这种材料的表面具有各种有机官能团的最大密度是一项重要的任务。在这些功能中,与金属物种作为配体的配位能力在许多领域(例如在催化领域)极为重要。本文描述了如何以纳米多孔有机硅材料的形式获得包含供体功能(例如羧基,硫代,螯合或胺基)的突出配体。详细研究了Co〜(II),Mn〜(II),V〜(IV)或Pt〜(IV)等金属中心的配位。报道了相应材料的磁性能及其在催化中的一些应用。显示了通过使用EPR光谱的距离测量来定量测定供体原子的表面密度。

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