化学
对映选择合成
星团(航天器)
立体化学
结晶学
有机化学
催化作用
计算机科学
程序设计语言
作者
Ying Lü,Xiu-Xia Ding,Ju-Suo Zhong,Zhan‐Guo Jiang,Cai‐Hong Zhan
标识
DOI:10.1021/acs.inorgchem.4c01635
摘要
Enantioselective synthesis of homochiral rare earth clusters is still a great challenge. In this work, we developed an efficient "cluster to cluster" approach, that is, a pair of enantiomerical R/S-{Nd8Fe3}-oxo clusters were successfully obtained from the presynthesized racemic {Nd9Fe2}-oxo cluster. R/S-hydrobenzoin ligands trigger the transformation of the pristine clusters by an SN2-like mechanism. Compared to the pristine cluster with an achiral core, the new cluster exhibits hierarchical chirality, from ligand chirality to interface chirality, then to helix chirality, and finally to supramolecular double helix chirality. The spectral experiments monitored the transformation and confirmed distinctly structure-related optical activity. The enantiomeric pure cluster also exhibits a potential asymmetric catalytic activity.
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