对映体药物
对映体
超分子化学
磷化氢
自组装
材料科学
手性(物理)
化学
结晶学
组合化学
立体化学
纳米技术
有机化学
对映选择合成
手征对称破缺
物理
晶体结构
催化作用
对称性破坏
量子力学
Nambu–Jona Lasinio模型
作者
Yanfei Zhu,Hui Wang,Kaiwei Wan,Jun Guo,Chun‐Ting He,Yue Yu,Luyang Zhao,Yin Zhang,Jiawei Lv,Lin Shi,Renxi Jin,Xin‐Xiang Zhang,Xinghua Shi,Zhiyong Tang
标识
DOI:10.1002/anie.201805695
摘要
Abstract Au 20 (PP 3 ) 4 Cl 4 (PP 3 =tris(2‐(diphenylphosphino)ethyl) phosphine), abbreviated as Au 20 , 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 Au 20 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 Au 20 in bulk, and an enantiomer excess ( ee ) value of as‐separated Au 20 of 97 %. As a result of its high purity, the distinctive optical activity of Au 20 , 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 Au 20 .
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