Wang Zhi, Sun Hao-Tian, Kurmoo Mohamedally, Liu Qing-Yun, Zhuang Gui-Lin, Zhao Quan-Qin, Wang Xing-Po, Tung Chen-Ho, Sun Di
Key Laboratory of Colloid and Interface Chemistry , Ministry of Education , School of Chemistry and Chemical Engineering , State Key Laboratory of Crystal Materials , Shandong University , Jinan , 250100 , People's Republic of China . Email:
Institut de Chimie de Strasbourg , Université de Strasbourg , CNRS-UMR 7177 , 4 rue Blaise Pascal , 67008 Strasbourg Cedex , France.
Chem Sci. 2019 Mar 29;10(18):4862-4867. doi: 10.1039/c8sc05666h. eCollection 2019 May 14.
Isomerization is highly important in all aspects of science, yet it is rarely observed in nanoscience. Here, we synthesized a unique triple core-shell Ag nanocluster displaying isomerism, which is controlled by different carboxylic acids and a one-way transformation ( → ). The innermost core is a rare Ag nanocluster which comprises an Ag octahedral unit as seen in face-centred cubic (fcc) silver metal and four capped Ag atoms. It templates two crescent-shaped polyoxometalate (WO) shells which are then enclosed in a shell of silver shaped as rugby balls. The organic ligands (PrS, PrCOO and PhCOO) finally shield the metallic clusters. Due to slight differences in structure at two poles and the steric hindrance of PrCOO and PhCOO, and adopt the shapes of flat-headed and cuspidal prolate spheres, respectively. Interestingly, PhCOOH is dominant over PrCOOH whereby crystals of were isolated if PhCOOH is added during the synthesis of . This demonstrates that PhCOOH not only alters the organic coats but also induces metal shell re-organization. This work reveals carboxylate-controlled skeletal isomerism in silver nanoclusters for the first time, thus deepening the understanding of silver nanocluster assembly, flexibility and reactivity.
异构化在科学的各个方面都非常重要,但在纳米科学中却很少被观察到。在此,我们合成了一种独特的具有异构现象的三核壳银纳米簇,其受不同羧酸和单向转变(→)的控制。最内层的核是一种罕见的银纳米簇,它包含一个面心立方(fcc)银金属中所见的银八面体单元和四个盖帽银原子。它为两个新月形的多金属氧酸盐(WO)壳提供模板,然后这两个壳被包裹在一个橄榄球形状的银壳中。有机配体(PrS、PrCOO和PhCOO)最终屏蔽金属簇。由于两极结构的细微差异以及PrCOO和PhCOO的空间位阻,和分别呈现平头和尖头长球体的形状。有趣的是,PhCOOH比PrCOOH占优势,因此如果在的合成过程中加入PhCOOH,就可以分离出的晶体。这表明PhCOOH不仅改变了有机涂层,还诱导了金属壳的重新组织。这项工作首次揭示了银纳米簇中羧酸盐控制的骨架异构现象,从而加深了对银纳米簇组装、柔韧性和反应性的理解。