期刊
JOURNAL OF PHYSICAL CHEMISTRY C
卷 118, 期 24, 页码 13018-13025出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp5037475
关键词
-
资金
- National Basic Research Program of China [2010CB923302, 2013CB834605]
- National Natural Science Foundation of China [21173200]
- Specialized Research Fund for the Doctoral Program of Higher Education of Ministry of Education [20113402110029]
- Chinese Academy of Sciences [2011T2J33]
The selective temperature-controlled surface-assisted synthesis of covalent, organometallic, and halogen-bonded nanomeshes based on a 3,5,3 '',5 ''-tetrabromo-para-terphenyl (TBrTP) precursor was studied with scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (STM) in ultrahigh vacuum. Vapor deposition of TBrTP onto Cu(111) at 90 K leads to a highly ordered organic monolayer stabilized by Br center dot center dot center dot Br and Br center dot center dot center dot H intermolecular bonds between the intact T-type assembled TBrTP molecules, as confirmed by density functional theory (DFT) calculations. Annealing the monolayer to 300 K results in C-Br bond scission and the formation of C-Cu-C bonds, which link adjacent para-terphenyl fragments such that stable organometallic frameworks are formed. Pore sizes correlate with the number of enclosed adatoms (most likely Br atoms), which presumably play a size-determining role during the process of the pore formation. Larger islands of the organometallic framework are obtained by deposition of TBrTP onto the copper surface held at 460 K. A further increase in sample temperature to 570 K during deposition gives rise to the formation of covalent organic frameworks with pores of tetragonal and trigonal symmetry. The covalent nanostructures are not completely planar, but contain phenylene units which are tilted relative to the surface plane, most likely due to steric hindrance between the C-H bonds inside the pores. Comparison of the three different bonding regimes reveals that the degree of long-range order correlates inversely with the strength of the bonds between the building blocks.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据