Understanding molecular self-assembly of a diol compound by considering competitive interactions

被引：6
|
作者：
Arado, Oscar Diaz [1 ,2 ]
Luft, Maike [1 ,2 ]
Moenig, Harry [1 ,2 ]
Held, Philipp Alexander [3 ]
Studer, Armido [3 ]
Amirjalayer, Saeed [1 ,2 ,4 ]
Fuchs, Harald [1 ,2 ]
机构：
[1] Univ Munster, Inst Phys, Wilhelm Klemm Str 10, D-48149 Munster, Germany
[2] Ctr Nanotechnol CeNTech, Heisenbergstr 11, D-48149 Munster, Germany
[3] Univ Munster, Inst Organ Chem, Corrensstr 40, D-48149 Munster, Germany
[4] Univ Munster, Ctr Multiscale Theory & Computat, Wilhelm Klemm Str 10, D-48149 Munster, Germany
来源：
PHYSICAL CHEMISTRY CHEMICAL PHYSICS | 2016年 / 18卷 / 39期
关键词：
METAL; AG(111); SURFACES; CU(100); FILMS;
D O I：
10.1039/c6cp05818c
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：
With a combination of scanning tunneling microscopy and density functional theory, effects on molecular self-assembly involving two distinct chemical groups were investigated. We analyzed the influence of the individual functional units in the adsorbate and extracted the dominating contributions to the adsorption behaviour. The viability of such a systematic approach to study self-assembled structures by considering the interplay between substrate effects and molecular design is demonstrated.
引用
收藏
页码：27390 / 27395
页数：6
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