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Polyionic Nanoclays: Tailorable Hybrid Organic-Inorganic Catalytic Platforms

机译:聚偶纳米载体:可批定可批定杂种有机 - 无机催化平台

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We unveil the synthesis and initial application of a hybrid inorganic-organic architecture comprising two-dimensional, few nanometer-thick magnesium phyllo(organo)silicate nanosheets displaying an ordered array of covalently linked imidazolium functionalities. Accessible via a simple, one-pot ambient-temperature synthesis using a custom organosiloxane, these so-called polyionic nanoclays (PINCs) represent an emergent class of supported ionic liquid phase and hold a number of attractive features, including: (i) an extremely high ionic density (e.g., 3.8 mmol g(-1) for the 1-methyl-3-propylimidazolium chloride PINC, roughly two-thirds the imidazolium cation density observed in the analogous free-flowing ionic liquid); (ii) the exchangeability of the associated counteranions to impart supplementary functionality or modulate solvent dispersibility; and (iii) the facility for tailoring the organic component, for example incorporating different (e.g., pyrrolidinium, pyridinium, phosphonium) or mixed onium moieties by employing the appropriate organosiloxane precursor(s). As a preliminary investigation of PINCs as nanocatalytic supports, we performed anion exchange with [AuCl4](-), followed by in situ reduction to generate small (<5 nm gold nanoparticles (AuNPs) on the clay lamellae. The resulting nanosized gold-modified PINCs dispersed in water exhibited an astonishing turnover frequency of 25 000 h(-1) for 4-nitrophenol reduction at room temperature, making this hybrid material the most active gold nanocatalyst reported for this model reaction. Most remarkably, AuNPs supported on the PINC showed a dramatically enhanced catalytic activity (4000% increase) compared to similar gold nanoparticles suspended in water (600 h(-1)), suggesting a major synergistic effect arising from the PINC support. Overall, the generality and flexibility of this route to lamellar hybrid nanoclays, coupled with the ability to accommodate a wide range of pendant organic ionic moieties suggests an auspicious future for PINCs in catalysis, ion exchange, energy storage, separations, (bio)sensing, imaging, and the construction of nanoscale assemblies.
机译:我们展示了一种无机-有机杂化结构的合成和初步应用,该结构由二维、几纳米厚的层状(有机)硅酸盐镁纳米片组成,显示了共价连接咪唑功能的有序阵列。这些所谓的聚离子纳米粘土(PICs)可通过使用定制有机硅氧烷的简单一锅室温合成获得,代表了一类新兴的负载型离子液体相,并具有许多吸引人的特征,包括:(i)1-甲基-3-丙基咪唑氯化物PICs具有极高的离子密度(例如,3.8 mmol g(-1)),大约是在类似自由流动离子液体中观察到的咪唑阳离子密度的三分之二);(ii)相关反阴离子的可交换性,以赋予补充功能或调节溶剂分散性;以及(iii)通过使用适当的有机硅氧烷前体来剪裁有机组分的设施,例如结合不同的(例如,吡咯烷、吡啶、磷)或混合的铵部分。作为PICs作为纳米催化载体的初步研究,我们与[AuCl4](-)进行阴离子交换,然后原位还原,在粘土片层上生成小于5 nm的金纳米粒子(AuNP)。由此产生的分散在水中的纳米金改性PICs在室温下对4-硝基苯酚还原时表现出惊人的25 000 h(-1)的翻转频率,使这种杂化材料成为该模型反应中报道的最活跃的金纳米催化剂。最值得注意的是,与悬浮在水中的类似金纳米颗粒(600小时(-1))相比,在PINC上负载的AuNPs显示出显著增强的催化活性(增加4000%),这表明PINC载体产生了重大的协同效应。总的来说,这种层状杂化纳米粘土路线的通用性和灵活性,再加上能够容纳广泛的悬垂有机离子部分,表明PINC在催化、离子交换、储能、分离、(生物)传感、成像和纳米组装构造方面有着良好的前景。

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