Spontaneous chiral self-assembly of CdSe@CdS nanorods

被引:19
|
作者
Duan, Tianwei [1 ]
Ai, Jing [2 ]
Cui, Xiaoyan [3 ]
Feng, Xiaowei [3 ]
Duan, Yingying [2 ]
Han, Lu [2 ]
Jiang, Jingang [3 ]
Che, Shunai [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Key Lab Mol Engn Chiral Drugs, State Key Lab Composite Mat, Sch Chem & Chem Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Tongji Univ, Sch Chem Sci & Engn, 1239 Siping Rd, Shanghai 200092, Peoples R China
[3] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem Sci & Chem Proc, 3663 North Zhongshan Rd, Shanghai 200062, Peoples R China
来源
CHEM | 2021年 / 7卷 / 10期
基金
中国国家自然科学基金;
关键词
CIRCULARLY-POLARIZED LUMINESCENCE; SYMMETRY-BREAKING; SEEDED GROWTH; NANOPARTICLES; NANOWIRES; DRIVEN; CDTE;
D O I
10.1016/j.chempr.2021.06.009
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The enantiomeric excess phenomenon in spontaneous chiral symmetry breaking (SCSB) is a crucial issue in the origin of homochirality in nature, whereas chiral inorganic compounds have long been reckoned as racemates. Here, we report the SCSB in the self-assembly of cadmium chalcogenide nanorods, leading to chiral biases away from the racemate. In the presence of achiral organics, helical CdSe@CdS nanorods (HCCNs) with unidirectionally rotated crystal lattices along the rod axis were stochastically formed on the epitaxial interface of the {111}cub/{0001} hex planes. The stability of helical dislocation structures, as supported by a theoretical analysis of their binding energies, suggested the possibility of the emergence of helical structures in an achiral environment. Hierarchical chiral films induced by simple solvent evaporation self-assembly of HCCNs exhibited spontaneous enantiomeric excess between batches, which was speculated to be originated from the enantiomeric excess seed assembly that induce one-handedness dominated system based on the majority rules.
引用
收藏
页码:2695 / 2707
页数:13
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