Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore, Karnataka-560012, India.
Dalton Trans. 2018 Dec 11;47(48):17401-17411. doi: 10.1039/c8dt03854f.
We report a general strategy for the synthesis of metal nanosponges (M = Ag, Au, Pt, Pd, and Cu) using a capping agent dissolution method where addition of water to the M@BNHx nanocomposite affords the metal nanosponges. The B-H bond of the BNHx polymer gets hydrolysed upon addition of water and produces hydrogen gas bubbles which act as dynamic templates leading to the formation of nanosponges. The rate of B-H bond hydrolysis has a direct impact on the final nanostructure of the materials. The metal nanosponges were characterized using powder XRD, electron microscopy, XPS, and BET surface area analyzer techniques. The porous structure of these nanosponges offers a large number of accessible surface sites for catalytic reactions. The catalytic activity of these metal nanosponges has been demonstrated for the reduction of 4-nitrophenol where palladium exhibits the highest catalytic activity (k = 0.314 min-1). The catalytic activity of palladium nanosponge was verified for the tandem dehydrogenation of ammonia borane and the hydrogenation of nitroarenes to arylamines in methanol at room temperature. The reduction of various substituted nitroarenes was proven to be functional group tolerant except for a few halogenated nitroarenes (X = Br and I) and >99% conversion was noted within 30-60 min with high turnover frequencies (TOF) at low catalyst loading (0.1 mol%). The catalyst could be easily separated out from the reaction mixture via centrifugation and was recyclable over several cycles, retaining its porous structure.
我们报告了一种使用封端剂溶解法合成金属纳米海绵(M = Ag、Au、Pt、Pd 和 Cu)的通用策略,其中向 M@BNHx 纳米复合材料中加水会得到金属纳米海绵。BNHx 聚合物中的 B-H 键在加水后会发生水解,并产生氢气气泡,这些气泡充当动态模板,导致纳米海绵的形成。B-H 键水解的速率对材料的最终纳米结构有直接影响。使用粉末 X 射线衍射、电子显微镜、XPS 和 BET 表面积分析仪技术对金属纳米海绵进行了表征。这些纳米海绵的多孔结构为催化反应提供了大量可及的表面位点。这些金属纳米海绵的催化活性已在 4-硝基苯酚的还原中得到证明,其中钯表现出最高的催化活性(k = 0.314 min-1)。钯纳米海绵的催化活性已在氨硼烷的串联脱氢和硝基芳烃在甲醇中的加氢反应中得到验证,在室温下可以转化为芳胺。各种取代的硝基芳烃的还原被证明对官能团具有耐受性,除了少数卤代硝基芳烃(X = Br 和 I)外,在 30-60 分钟内即可达到 99%以上的转化率,并且在低催化剂负载量(0.1 mol%)下具有高的周转频率(TOF)。催化剂可以通过离心很容易地从反应混合物中分离出来,并可以在几个循环中重复使用,同时保持其多孔结构。