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[Ag(C≡C Bu)(CrO)]:一种由无机和有机配体共同保护的原子精确银纳米簇

[Ag(C≡C Bu)(CrO)]: An Atomically Precise Silver Nanocluster Co-protected by Inorganic and Organic Ligands.

作者信息

Zhang Shan-Shan, Alkan Fahri, Su Hai-Feng, Aikens Christine M, Tung Chen-Ho, Sun Di

机构信息

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.

Department of Chemistry , Kansas State University , Manhattan , Kansas 66506 , United States.

出版信息

J Am Chem Soc. 2019 Mar 13;141(10):4460-4467. doi: 10.1021/jacs.9b00703. Epub 2019 Feb 27.

Abstract

The elaborate selection of capping ligands is of great importance in the synthesis of atomically precise metal nanoclusters. Organic thiolates, alkynyls, phosphines, and/or their combinations are the ligands most widely utilized to protect metal nanoclusters, while inorganic oxo anions have been almost neglected in this field. Herein, the first CrO/ BuC≡C co-capped Ag nanocluster (SD/Ag48, SD = SunDi) was synthesized and structurally characterized by single-crystal X-ray diffraction. The pseudo-5-fold symmetric metal skeleton of SD/Ag48 shows a core-shell structure composed of a Ag cylinder encircled by an outer Ag shell. Unprecedentedly, coexistence of inorganic (CrO) and organic ( BuC≡C) ligands was observed on the surface of SD/Ag48. The inorganic CrO anion plays three important roles in the construction of silver nanoclusters: (i) passivating the Ag kernel; (ii) connecting the core and shell; and (iii) protecting the Ag shell. This nanocluster belongs to a 14e superatom system and exhibits successive molecule-like absorption bands from the visible to the ultraviolet region. This work not only establishes a fresh inorganic ligand strategy in the synthesis of silver nanoclusters but also provides a new insight into the important surface coordination chemistry of CrO in the shape control of silver nanoclusters.

摘要

在原子精确的金属纳米团簇的合成中,精心选择封端配体至关重要。有机硫醇盐、炔基、膦和/或它们的组合是用于保护金属纳米团簇最广泛使用的配体,而无机含氧阴离子在该领域几乎被忽视。在此,首次合成了CrO/BuC≡C共封端的Ag纳米团簇(SD/Ag48,SD = 孙迪),并通过单晶X射线衍射对其结构进行了表征。SD/Ag48的准五重对称金属骨架呈现出由一个Ag圆柱体被一个外部Ag壳包围组成的核壳结构。前所未有的是,在SD/Ag48的表面观察到无机(CrO)和有机(BuC≡C)配体的共存。无机CrO阴离子在银纳米团簇的构建中发挥三个重要作用:(i)钝化Ag核;(ii)连接核和壳;(iii)保护Ag壳。该纳米团簇属于14e超原子体系,并在从可见光到紫外区域呈现出连续的类分子吸收带。这项工作不仅在银纳米团簇的合成中建立了一种新的无机配体策略,而且为CrO在银纳米团簇形状控制中的重要表面配位化学提供了新的见解。

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