Ionic hydrogen bonds controlling two-dimensional supramolecular systems at a metal surface

被引:115
作者
Payer, Dietmar
Comisso, Alessio
Dmitriev, Alexandre
Strunskus, Thomas
Lin, Nian
Woell, Christof
DeVita, Alessandro
Barth, Johannes V.
Kern, Klaus
机构
[1] Max Planck Inst Festkorperforsch, D-70563 Stuttgart, Germany
[2] Univ Trieste, CENMAT, I-34127 Trieste, Italy
[3] INFM DEMOCRITOS Natl Simulat Ctr, Trieste, Italy
[4] Ruhr Univ Bochum, Lehrstuhl Phys Chem 1, D-44780 Bochum, Germany
[5] Kings Coll London, Dept Phys, London WC2R 2LS, England
[6] Ecole Polytech Fed Lausanne, Inst Phys Nanostruct, CH-1015 Lausanne, Switzerland
关键词
ab initio calculations; carboxylic acids; hydrogen bonds; scanning tunneling microscopy; supramolecular self-assembly;
D O I
10.1002/chem.200601325
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen-bond formation between ionic adsorbates on an Ag(III) surface under ultrahigh vacuum was studied by scanning tunneling microscopy/spectroscopy (STM/STS), Xray photoelectron spectroscopy (XPS), near-edge X-ray absorption fine structure (NEXAFS), and molecular dynamics calculations. The adsorbate, 1,3,5-benzenetricarboxylic acid (trimesic acid, TMA), self-assembles at low temperatures (250-300 K) into the known open honeycomb motif through neutral hydrogen bonds formed between carboxyl groups, whereas annealing at 420 K leads to a densely packed quartet structure consisting of flat-lying molecules with one deprotonated carboxyl group per molecule. The resulting charged carboxylate groups form intermolecular ionic hydrogen bonds with enhanced strength compared to the neutral hydrogen bonds; this represents an alternative supramolecular bonding motif in 2D supramolecular organization.
引用
收藏
页码:3900 / 3906
页数:7
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