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表面辅助烷烃聚合:结构-反应性关系研究。

Surface-Assisted Alkane Polymerization: Investigation on Structure-Reactivity Relationship.

机构信息

Jiangsu Key Laboratory for Carbon Based Functional Materials & Devices, Institute of Functional Nano & Soft Materials (FUNSOM) , Soochow University , Suzhou 215123 , People's Republic of China.

School of Physics & State Key Laboratory of Optoelectronic Materials and Technologies , Sun Yat-sen University , 510275 Guangzhou , People's Republic of China.

出版信息

J Am Chem Soc. 2018 Apr 11;140(14):4820-4825. doi: 10.1021/jacs.7b09097. Epub 2018 Feb 20.

Abstract

Surface-assisted polymerization of alkanes is a remarkable reaction for which the surface reconstruction of Au(110) is crucial. The surface of (1×2)-Au(110) precovered with molecules can be completely transformed into (1×3)-Au(110) by introducing branched methylidene groups on both sides of the aliphatic chain (18, 19-dimethylidenehexatriacontane) or locally shifted into (1×3)-Au(110) under exposure to low-energy electrons (beam energy from 3.5 to 33.6 eV, for alkane dotriacontane). Scanning tunneling microscopy investigations demonstrate that alkane chains adsorbed on (1×3)-Au(110) are more reactive than on (1×2)-Au(110), presenting a solid experimental proof for structure-reactivity relationships. This difference can be ascribed to the existence of an extra row of gold atoms in the groove of (1×3)-Au(110), providing active sites of Au atoms with lower coordination number. The experimental results are further confirmed by density functional theory simulations.

摘要

表面辅助的烷烃聚合反应是一种非常显著的反应,其中 Au(110) 的表面重构是至关重要的。通过在脂肪链的两侧引入支化亚甲基基团(18、19-二亚甲基三十六烷),或者在暴露于低能电子(电子束能量为 3.5 至 33.6eV,对于烷烃三十二烷)时局部转变为(1×3)-Au(110),(1×2)-Au(110) 预覆盖分子的表面可以完全转化为(1×3)-Au(110)。扫描隧道显微镜研究表明,吸附在(1×3)-Au(110)上的烷烃链比吸附在(1×2)-Au(110)上更具反应性,为结构-反应性关系提供了坚实的实验证据。这种差异可以归因于(1×3)-Au(110)的凹槽中存在额外的一排金原子,为具有较低配位数的金原子提供了活性位点。实验结果进一步通过密度泛函理论模拟得到证实。

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