STM study of terephthalic acid self-assembly on Au(III): Hydrogen-bonded sheets on an inhomogeneous substrate

被引:171
|
作者
Clair, S
Pons, S
Seitsonen, AP
Brune, H
Kern, K
Barth, JV [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Phys Nanostruct, CH-1015 Lausanne, Switzerland
[2] Univ Zurich, Inst Chem Phys, CH-8057 Zurich, Switzerland
[3] Max Planck Inst Festkorperforsch, D-70569 Stuttgart, Germany
[4] Univ British Columbia, Adv Mat & Proc Engn Lab, Vancouver, BC V6T 1Z4, Canada
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2004年 / 108卷 / 38期
关键词
D O I
10.1021/jp049501n
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
The adsorption and ordering of the molecule terephthalic acid (TPA), 1,4-benzene-dicarboxylic acid C6H4-(COOH)(2), on the reconstructed Au(111) surface has been studied in situ in ultrahigh vacuum by scanning tunneling microscopy (STM) at room temperature. Two-dimensional (2D) self-assembled supramolecular domains evolve, wherein the well-known one-dimensional (1D) carboxyl H-bond pairing scheme is identified. Since the individual molecules occupy a distinct adsorption site and the supramolecular ordering usually extends over several substrate reconstruction domains, a significant variation in hydrogen bond lengths is encountered, which illustrates the versatility of hydrogen bridges in molecular engineering at surfaces. Ab initio calculations for a 1D H-bonded molecular chain provide insight into the limited geometric response of the molecules in different local environments.
引用
收藏
页码:14585 / 14590
页数:6
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