Self-assembly processes of 2D Au(<sc>i</sc>)-S(CH2)2COOH lamellae

被引:0
|
作者
Zhang, Shengrui [1 ]
Yu, Zhongqi [1 ]
Demessence, Aude [2 ]
Guillou, Nathalie [3 ]
Xu, Shujue [1 ]
Liu, Han [1 ]
Fu, Yuru [1 ]
Zhang, Jingpei [1 ]
Li, Minjie [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China
[2] Univ Claude Bernard Lyon 1, Univ Lyon, Inst Rech Catalyse & Environm Lyon IRCELYON, CNRS, Villeurbanne, France
[3] Univ Paris Saclay, Inst Lavoisier Versailles, UVSQ, CNRS,UMR 8180, F-78000 Versailles, France
基金
中国国家自然科学基金;
关键词
GOLD(I)-ALKANETHIOLATE COMPLEXES; GOLD; CLUSTERS;
D O I
10.1039/d4nr05118a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solving the assembled structure of Au(i)-thiolate linear coordination polymers has been a challenging task as they generally lack good crystallinity. This has prevented the elucidation of their assembly processes at the molecular level. In this paper, selected area electron diffraction (SAED) patterns of two-dimensional (2D) Au(i)-S(CH2)2COOH (Au(i)-MPA) lamellae are obtained by applying cryogenic transmission electron microscopy. The SAED patterns allow to propose a packing mode of Au(i)-MPA chains in the 2D structure by comparison with the crystal structure of Ag(i)-MPA solved from powder X-ray diffraction. Then, multi-step self-assembly processes to 2D lamellae via the aggregation and crystallization of an intermediate of 1D pre-assemblies are disclosed, which explains the difficulty in synthesize their large single crystals. Based on these results, 2D Au(i)-MPA lamellae with tunable sizes and degrees of crystallinity are synthesized by kinetic control of solvent composition and temperature.
引用
收藏
页码:5270 / 5279
页数:10
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