Steering Surface Reaction Dynamics with a Self-Assembly Strategy: Ullmann Coupling on Metal Surfaces

被引:58
|
作者
Zhou, Xiong [1 ]
Wang, Chenguang [2 ]
Zhang, Yajie [1 ]
Cheng, Fang [1 ]
He, Yang [1 ]
Shen, Qian [1 ]
Shang, Jian [1 ]
Shao, Xiang [3 ]
Ji, Wei [2 ]
Chen, Wei [4 ]
Xu, Guoqin [4 ]
Wu, Kai [1 ]
机构
[1] Peking Univ, BNLMS Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[2] Renmin Univ China, Dept Phys, Beijing 100872, Peoples R China
[3] Univ Sci & Technol China, Dept Chem Phys, Sch Chem & Mat Sci, Hefei 230026, Peoples R China
[4] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
关键词
scanning tunneling microscopy; self-assembly strategies; surface reaction dynamics; Ullmann coupling; GRAPHENE NANORIBBONS; MONOLAYERS; RADICALS; CU(111); INSIGHT; BOTTOM; POLYMERIZATION; MACROCYCLES; MECHANISMS; EFFICIENCY;
D O I
10.1002/anie.201705018
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ullmann coupling of 4-bromobiphenyl thermally catalyzed on Ag(111), Cu(111), and Cu(100) surfaces was scrutinized by scanning tunneling microscopy as well as theoretical calculations. Detailed experimental evidence showed that initial formation of organometallic intermediates on the surface, as self-assembled structures or sparsely dispersed species, is determined by the subsequent reaction pathway. Specifically, the assembled organometallic intermediates at full coverage underwent a single-barrier process to directly convert into the final coupling products, while the sparsely dispersed intermediates at low coverage went through a double-barrier process via newly identified clover-shaped intermediates prior to formation of the final coupling products. These findings demonstrate that a self-assembly strategy can efficiently steer surface reaction pathways and dynamics.
引用
收藏
页码:12852 / 12856
页数:5
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