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Integration of Ag/AgCl and Au nanoparticles into isostructural porous coordination polymers of Ni(II), Co(II) and Mn(II): magnetic studies

机译:将Ag / AgCl和Au纳米粒子整合到Ni(II),Co(II)和Mn(II)的同构多孔配位聚合物中:磁性研究

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A systematic investigation of silver/silver chloride (Ag/AgCl) and gold (Au) nanoparticle (NP) formation within non-activated isostructural porous coordination polymers (PCPs) namely Ni-PCP, Co-PCP and Mn-PCP at room temperature is reported without the use of any reducing agent and deterioration of host frameworks. A supercharged environment due to the presence of free anions make these PCPs suitable templates for the growth of nanoparticles (NPs) in high yields. High resolution transmission electron microscopy (HRTEM) images provided insight into the size, shape and distribution of the NPs within the frameworks. Different shapes and sizes of the NPs are attributed to the differences in the levels of supramolecular interactions within these isostructural series and the ionic radii which is related to the charge density of metal nodes. From an electron paramagnetic resonance (EPR) study it is evidenced that synthesis of Au NPs in Ni-PCP is completely through redox reaction via strong charge transfer between coordinated metal and the metal precursor, and the others are via acid formation through anions present in the cavities of PCPs. Au NPs integrated frameworks display different soft ferromagnetic properties when placed in a magnetic field at room temperature.
机译:对室温下非活化的等结构多孔配位聚合物(PCP)(即Ni-PCP,Co-PCP和Mn-PCP)中银/氯化银(Ag / AgCl)和金(Au)纳米颗粒(NP)形成的系统研究是报告没有使用任何还原剂和宿主框架的恶化。由于存在游离阴离子,增压环境使这些PCP成为适合以高产率生长纳米颗粒(NP)的模板。高分辨率透射电子显微镜(HRTEM)图像提供了对框架内NP的大小,形状和分布的深入了解。 NP的不同形状和大小归因于这些同构系列中超分子相互作用水平的不同以及与金属节点电荷密度有关的离子半径。从电子顺磁共振(EPR)研究中可以证明,Ni-PCP中Au NPs的合成完全是通过配位金属与金属前体之间强电荷转移的氧化还原反应完成的,而其他<通过存在于五氯苯酚空腔中的阴离子形成酸。当置于室温下的磁场中时,金纳米粒子集成框架显示出不同的软铁磁特性。

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