期刊
INORGANIC CHEMISTRY COMMUNICATIONS
卷 124, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.inoche.2020.108389
关键词
Co-crystallization induced emission; Crystalline state; Amorphous state; Noncovalent interactions; Photoluminescence
资金
- PHD Start-up Fund of XPU [107020489]
- Shaanxi Provincial Education Department [20JK0655, 19JK0365]
- Natural Science Basis Research Plan in Shaanxi Province of China [2020JQ-821]
This work reports the phenomenon of co-crystallization induced emission in two atomically precise and different size nanoclusters for the first time, characterized by single-crystal X-ray crystallography. The enhanced radiative transitions in the crystalline state are attributed to the significant restriction of intra- and inter-molecular vibrations by noncovalent interactions in the nanoclusters' crystalline state.
In this work, for the first time we report the co-crystallization induced emission phenomenon in the co crystallization of two atomically precise and different size nanlclusters, a fusiform Ag26Au(2-EBT)(18)(PPh3)(6) and a spherical Ag24Au(2-EBT)(18) (2-EBT = 2-Ethylbenzenethiol), characterized by single-crystal X-ray crystallography. A plausible explanation for this interesting phenomenon is that noncovalent interactions (such as pi center dot center dot center dot pi and C-H center dot center dot center dot pi interactions) in crystalline state of nanoclusters significantly restrict the intraand inter-molecular vibrations and thus result in considerably enhance the radiative transitions in the crystalline state.
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