Template-Assisted Proximity for Oligomerization of Fullerenes

被引:10
作者
Cheng, Kum-Yi
Lee, Shern-Long [2 ]
Kuo, Ting-Yang [3 ]
Lin, Chih-Hsun
Chen, Yen-Chen
Kuo, Ting-Hao
Hsu, Cheng-Chih
Chen, Chun-Hsien [1 ]
机构
[1] Natl Taiwan Univ, Dept Chem, 1 Sec 4,Roosevelt Rd, Taipei 10617, Taiwan
[2] Shenzhen Univ, Inst Adv Study, Shenzhen 518060, Guangdong, Peoples R China
[3] Minist Sci & Technol, Dept Nat Sci & Sustainable Dev, Taipei 10622, Taiwan
关键词
LIQUID-SOLID INTERFACE; HOST-GUEST CHEMISTRY; SUPRAMOLECULAR CHEMISTRY; C-60; MONOLAYER; NETWORKS; CARBON; DIMER; 2D; SURFACE; ACID;
D O I
10.1021/acs.langmuir.8b00314
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Demonstrated herein is an unprecedented porous template-assisted reaction at the solid-liquid interface involving bond formation, which is typically collision-driven and occurs in the solution and gas phases. The template is a TMA (trimesic acid) monolayer with two-dimensional pores that host fullerenes, which otherwise exhibit an insignificant affinity to an undecorated graphite substrate. The confinement of C-84 units in the TMA pores formulates a proximity that is ideal for bond formation. The oligomerization of C-84 is triggered by an electric pulse via a scanning tunneling microscope tip. The spacing between C-84 moieties becomes 1.4 nm, which is larger than the edge-to-edge diameter of 1.1-1.2 nm of C-84 due to the formation of intermolecular single bonds. In addition, the characteristic mass-to-charge ratios of dupers and trimers are observed by mass spectrometry. The experimental findings shed light on the active role of spatially tailored templates in facilitating the chemical activity of guest molecules.
引用
收藏
页码:5416 / 5421
页数:6
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