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Thermodynamic-Driven Self-Assembly: Heterochiral Self-Sorting and Structural Reconfiguration in Gold(I)–Sulfido Cluster System
Author(s) -
LiaoYuan Yao,
Terence KwokMing Lee,
Vivian WingWah Yam
Publication year - 2016
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.6b03844
Subject(s) - chemistry , chirality (physics) , enantiomer , cluster (spacecraft) , self assembly , stereochemistry , planar chirality , crystallography , chiral symmetry breaking , symmetry breaking , organic chemistry , enantioselective synthesis , catalysis , physics , quantum mechanics , computer science , nambu–jona lasinio model , programming language
By employing chiral precursors, a new class of chiral gold(I)-sulfido clusters with unique structures has been constructed. Interestingly, pure enantiomers of the precursors are found to self-assemble into chiral hexa- and decanuclear clusters sequentially, while a racemic mixture of them has resulted in heterochiral self-sorting of an achiral meso decanuclear cluster. Chirality has determined not only the symmetry and structures but also the photophysical behaviors of these clusters. The racemic mixture of decanuclear clusters undergoes rearrangement and heterochiral self-sorting to give a meso decanuclear cluster. The thermodynamic-driven heterochiral self-sorting of gold(I) clusters provides a means to develop controlled self-assembly that may be of relevance to the understanding of chirality in nature.

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