溶剂
化学
液态液体
接口(物质)
材料科学
手性(物理)
化学工程
分子
有机化学
色谱法
手征对称性
物理
吉布斯等温线
量子力学
Nambu–Jona Lasinio模型
工程类
夸克
作者
Matsuhiro Maeda,Steven De Feyter,Kazukuni Tahara
出处
期刊:Langmuir
[American Chemical Society]
日期:2024-07-10
卷期号:40 (29): 15071-15079
标识
DOI:10.1021/acs.langmuir.4c01430
摘要
We herein investigate the formation of homochiral hierarchical self-assembled molecular networks (SAMNs) via chirality induction by the coadsorption of a chiral solvent at the liquid/graphite interface by means of scanning tunneling microscopy (STM). In a mixture of achiral solvents, 1-hexanoic acid, and 1,2,4-trichlorobenzene, an achiral dehydrobenzo[12]annulene (DBA) derivative with three alkoxy and three hydroxy groups in an alternating manner forms chiral hierarchical triangular cluster structures through dynamic self-sorting. Enantiomorphous domains appear in equal probability. On the other hand, in chiral 2-methyl-1-hexanoic acid as a solvent, this molecule produces (i) homochiral small triangular clusters at a low solute concentration, (ii) a chirality-biased hierarchical structure consisting of triangular cluster structures with different cluster sizes at a medium concentration, and (iii) a dense structure with no chirality bias at a high concentration. We attribute the concentration-dependent degree of the chirality transmission to the number of coadsorbed solvent molecules in the SAMNs and to the difference in nucleus structure and size in the initial stage of the SAMN formation.
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