Construction of Two-Dimensional Organometallic Coordination Networks with Both Organic Kagome and Semiregular Metal Lattices on Au(111)

被引:0
|
作者
Kang, Li-Xia [1 ]
Wang, Bing-Xin [1 ]
Zhang, Xin-Yu [1 ]
Zhu, Ya-Cheng [1 ]
Li, Deng-Yuan [1 ,2 ]
Liu, Pei-Nian [1 ,2 ]
机构
[1] East China Univ Sci & Technol, Sch Chem & Mol Engn, State Key Lab Chem Engn, Shanghai Key Lab Funct Mat Chem,Key Lab Adv Mat, Shanghai 200237, Peoples R China
[2] China Pharmaceut Univ, Key Lab Nat Med Dept Med Chem, Nanjing 211198, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2024年 / 15卷 / 23期
基金
中国国家自然科学基金;
关键词
ELECTRON LOCALIZATION; INTERMEDIATE; POLYMERIZATION; ADSORPTION; CHEMISTRY; CHAINS; STATES;
D O I
10.1021/acs.jpclett.4c01192
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two-dimensional metal-organic networks (2D MONs) having heterogeneous coordination nodes (HCNs) could exhibit excellent performance in catalysis and optoelectronics because of the unbalanced electron distribution of the coordinating metals. Therefore, the design and construction of 2D MONs with HCNs are highly desirable but remain challenging. Here, we report the construction of 2D organometallic coordination networks with an organic Kagome lattice and a semiregular metal lattice on Au(111) via the in situ formation of HCNs. Using a bifunctional precursor 1,4-dibromo-2,5-diisocyanobenzene, the coordination of isocyano with Au adatom on a room-temperature Au(111) yielded metal-organic coordination chains with isocyano-Au-isocyano nodes. In contrast, on a high-temperature Au(111), a selective debromination/coordination cascade reaction occurred, affording 2D organometallic coordination networks with phenyl-Au-isocyano nodes. By combining scanning tunneling microscopy and density functional theory calculations, we determined the structures of coordination products and the nature of coordination nodes, demonstrating a thermodynamically favorable pathway for forming the phenyl-Au-isocyano nodes.
引用
收藏
页码:6108 / 6114
页数:7
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