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银表面上的中间态导向手性转移

Intermediate States Directed Chiral Transfer on a Silver Surface.

作者信息

Yang Biao, Cao Nan, Ju Huanxin, Lin Haiping, Li Youyong, Ding Honghe, Ding Jinqiang, Zhang Junjie, Peng Chencheng, Zhang Haiming, Zhu Junfa, Li Qing, Chi Lifeng

机构信息

Institute of Functional Nano and Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials a Devices , Soochow University , 199 Ren'ai Road , Suzhou 215123 , P. R. China.

National Synchrotron Radiation Laboratory and Collaborative Innovation Center of Suzhou Nano Science and Technology , University of Science and Technology of China , Hefei , Anhui 230029 , China.

出版信息

J Am Chem Soc. 2019 Jan 9;141(1):168-174. doi: 10.1021/jacs.8b05699. Epub 2018 Dec 18.

Abstract

Chiral synthesis on surfaces has acquired tremendous interest. We herein report a novel approach of two-dimensional chiral transfer directed by metal-organic intermediate states on a silver surface. With initial deposition at low temperature, the achiral 4,4'-dihydroxybiphenyl molecules self-assemble into large scale two-dimensional networks with 4-fold symmetry via intermolecular hydrogen bonding. Fine controlled annealing, however, leads to the formation of tetramer-like chiral metal-organic hybrids, which self-organize into enantiomeric islands on the Ag(100) surface. Subsequent ortho C-C couplings of the reactants lead to dimer products. Of great importance, the chirality expressions of the dimer products are observed to be transferred directly from that of the tetramer intermediate states. The detailed reaction pathways are rationalized by DFT calculations and synchrotron-based XPS experiments, demonstrating the mechanisms of the chiral transfer.

摘要

表面手性合成已引起了极大的关注。我们在此报告一种在银表面由金属有机中间态引导的二维手性转移的新方法。在低温下初始沉积时,非手性的4,4'-二羟基联苯分子通过分子间氢键自组装成具有四重对称性的大规模二维网络。然而,精细控制的退火会导致形成四聚体状的手性金属有机杂化物,它们在Ag(100)表面自组织成对映体岛。反应物随后的邻位C-C偶联产生二聚体产物。非常重要的是,观察到二聚体产物的手性表达直接从四聚体中间态转移而来。详细的反应途径通过密度泛函理论(DFT)计算和基于同步加速器的X射线光电子能谱(XPS)实验得到了合理化,证明了手性转移的机制。

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