Complex Interplay and Hierarchy of Interactions in Two-Dimensional Supramolecular Assemblies

被引:46
作者
Canas-Ventura, Marta E. [2 ,4 ]
Ait-Mansour, Kamel [2 ,4 ]
Ruffieux, Pascal [4 ]
Rieger, Ralph [3 ]
Muellen, Klaus [3 ]
Brune, Harald [2 ]
Fasel, Roman [1 ,4 ]
机构
[1] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
[2] Ecole Polytech Fed Lausanne, ICMP, Stn 3, CH-1015 Lausanne, Switzerland
[3] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[4] Empa, Swiss Fed Labs Mat Sci & Technol, Nanotech Surfaces Lab, CH-3602 Thun, Switzerland
基金
瑞士国家科学基金会;
关键词
self-assembly; hydrogen bonding; dipolar interaction; metal coordination; scanning tunneling microscopy; HYDROGEN-BONDED NETWORKS; MOLECULAR TECTONICS; NONCOVALENT SYNTHESIS; ORGANIC-MOLECULES; SURFACE; DERIVATIVES; CLUSTERS; CHIRALITY; MELAMINE; AU(111);
D O I
10.1021/nn102164g
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
In order to address the interplay of hydrogen bonding, dipolar interactions, and metal coordination, we have investigated the two-dimensional mono- and bicomponent self-assembly of three closely related diaminotriazine-based molecular building blocks and a complementary perylenetetracarboxylic diimide by means of scanning tunneling microscopy The simplest molecular species, bis-diaminotriazine-benzene, only interacts via hydrogen bonds and forms a unique supramolecular pattern on the Au(111) surface. For the two related molecular species, which exhibit in addition to hydrogen bonding also dipolar interactions and metal coordination, the number of distinct supramolecular structures increases dramatically with the number of possible Interaction channels. Deposition together with the complementary perylene species, however, always results In, a single well-defined supramolecular arrangement of molecules. A detailed analysis of the observed mono- and bicomponent assemblies allows shedding light on the hierarchy of the competing interactions, with important implications for the fabrication of surface supported supramolecular networks by design.
引用
收藏
页码:457 / 469
页数:13
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