Steering molecular organization and host-guest interactions using two-dimensional nanoporous coordination systems

被引:609
作者
Stepanow, S
Lingenfelder, M
Dmitriev, A
Spillmann, H
Delvigne, E
Lin, N
Deng, XB
Cai, CZ
Barth, JV
Kern, K
机构
[1] Max Planck Inst Festkorperforsch, D-70569 Stuttgart, Germany
[2] Ecole Polytech Fed Lausanne, Inst Phys Nanostruct, CH-1015 Lausanne, Switzerland
[3] Univ Houston, Dept Chem, Houston, TX 77204 USA
[4] Univ Houston, Ctr Mat Chem, Houston, TX 77204 USA
[5] Univ British Columbia, Adv Mat & Proc Engn Lab, Vancouver, BC V6T 1Z4, Canada
关键词
D O I
10.1038/nmat1088
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
Metal - organic coordination networks (MOCNs) have attracted wide interest because they provide a novel route towards porous materials that may find applications in molecular recognition, catalysis, gas storage and separation(1,2). The so-called rational design principle - synthesis of materials with predictable structures and properties - has been explored using appropriate organic molecular linkers connecting to metal nodes to control pore size and functionality of open coordination networks(3-9). Here we demonstrate the fabrication of surface-supported MOCNs comprising tailored pore sizes and chemical functionality by the modular assembly of polytopic organic carboxylate linker molecules and iron atoms on a Cu(100) surface under ultra-high-vacuum conditions. These arrays provide versatile templates for the handling and organization of functional species at the nanoscale, as is demonstrated by their use to accommodate C-60 guest molecules. Temperature-controlled studies reveal, at the single-molecule level, how pore size and chemical functionality determine the host - guest interactions.
引用
收藏
页码:229 / 233
页数:5
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