Molecular Motions in AIEgen Crystals: Turning on Photoluminescence by Force-Induced Filament Sliding

化学 蛋白质丝 光致发光 纳米技术 光电子学 生物化学 物理 材料科学
作者
Jing Zhang,Benzhao He,Wenjie Wu,Parvej Alam,Han Zhang,Junyi Gong,Fengyan Song,Zaiyu Wang,Herman H. Y. Sung,Ian D. Williams,Zhiming Wang,Jacky W. Y. Lam,Ben Zhong Tang
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:142 (34): 14608-14618 被引量:71
标识
DOI:10.1021/jacs.0c06305
摘要

Life process is amazing, and it proceeds against the eternal law of entropy increase through molecular motion and takes energy from the environment to build high-order complexity from chaos to achieve evolution with more sophisticated architectures. Inspired from the elegance of life process and also to effectively exploit the undeveloped solid-state molecular motion, two unique chiral Au(I) complexes were elaborately developed in this study, in which their powders could realize a dramatic transformation from nonemissive isolated crystallites to emissive well-defined microcrystals under the stimulation of mechanical force. Such an unusual crystallization was presumed to be caused by molecular motions driven by the formation of strong aurophilic interactions as well as multiple C-H···F and π-π interactions. Such a prominent macroscopic off/on luminescent switching could also be achieved through extremely subtle molecular motions in the crystal state and presented a filament sliding that occurred in a layer-by-layer molecular stacking fashion with no involvement of any crystal phase transition. Additionally, it had been demonstrated that the manipulation of the solid-state molecular motions could result in the generation of circularly polarized luminescence.
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