| Literature DB >> 30835442 |
Jing Zhang1, Qiuming Liu2,3, Wenjie Wu1, Junhui Peng1, Haoke Zhang1, Fengyan Song1, Benzhao He1, Xiaoyan Wang4, Herman H-Y Sung1, Ming Chen1, Bing Shi Li2, Sheng Hua Liu4, Jacky W Y Lam1, Ben Zhong Tang1,3.
Abstract
Constructing artificial helical structures through hierarchical self-assembly and exploring the underlying mechanism are important, and they help gain insight from the structures, processes, and functions from the biological helices and facilitate the development of material science and nanotechnology. Herein, the two enantiomers of chiral Au(I) complexes ( S)-1 and ( R)-1 were synthesized, and they exhibited impressive spontaneous hierarchical self-assembly transitions from vesicles to helical fibers. An impressive chirality inversion and amplification was accompanied by the assembly transition, as elucidated by the results of in situ and time-dependent circular dichroism spectroscopy and scanning electron microscope imaging. The two enantiomers could serve as ideal chiral templates to co-assemble with other achiral luminogens to efficiently induce the resulting co-assembly systems to show circularly polarized luminescence (CPL). Our work has provided a simple but efficient way to explore the sophisticated self-assembly process and presented a facile and effective strategy to fabricate architectures with CPL properties.Entities:
Keywords: aggregation-induced emission; circularly polarized luminescence; gold complex; hierarchical self-assembly; real-time monitoring
Mesh:
Substances:
Year: 2019 PMID: 30835442 DOI: 10.1021/acsnano.9b00218
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881