| Literature DB >> 29877009 |
Yanfei Zhu1,2, Hui Wang1, Kaiwei Wan1,2, Jun Guo1,2, Chunting He3, Yue Yu4, Luyang Zhao2, Yin Zhang1,2, Jiawei Lv1, Lin Shi1, Renxi Jin4, Xinxiang Zhang4, Xinghua Shi1, Zhiyong Tang1.
Abstract
Au20 (PP3 )4 Cl4 (PP3 =tris(2-(diphenylphosphino)ethyl) phosphine), abbreviated as Au20 , is the only Au nanocluster with an intrinsically chiral core without a chiral environment (chiral ligands or Au-thiolate staples), making it a unique object to understand chiral evolution and explore chiral applications. Unfortunately, the synthesized Au20 is racemic, and its enantiomers have not yet been separated. Herein, we report a supramolecular assembly strategy with α-cyclodextrin (α-CD) to afford enantiopure Au20 in bulk, and an enantiomer excess (ee) value of as-separated Au20 of 97 %. As a result of its high purity, the distinctive optical activity of Au20 , which originates from electronic transitions confined in chiral cores, is fully explored. Theoretical studies reveals that the enantioseparation results from the preferential self-assembly of α-CD with organic ligands on the surface of right-handed Au20 .Entities:
Keywords: chirality; cyclodextrins; gold; nanoclusters; supramolecular chemistry
Year: 2018 PMID: 29877009 DOI: 10.1002/anie.201805695
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336