On-surface synthesis on a bulk insulator surface

被引:10
|
作者
Richter, Antje [1 ]
Floris, Andrea [2 ]
Bechstein, Ralf [1 ]
Kantorovich, Lev [3 ]
Kuehnle, Angelika [1 ,4 ]
机构
[1] Johannes Gutenberg Univ Mainz, Inst Phys Chem, Duesbergweg 10-14, D-55099 Mainz, Germany
[2] Univ Lincoln, Sch Math & Phys, Lincoln LN6 7TS, England
[3] Kings Coll London, Dept Phys, London WC2R 2LS, England
[4] Bielefeld Univ, Dept Chem, Phys Chem 1, Univ Str 25, D-33615 Bielefeld, Germany
基金
英国工程与自然科学研究理事会;
关键词
on-surface synthesis; bulk insulator; calcite; dynamic atomic force microscopy; molecular electronics; electronic decoupling; density functional theory; FUNCTIONAL-GROUP ADSORPTION; AZIDE-ALKYNE CYCLOADDITION; TUNNELING MICROSCOPE TIP; CHAIN POLYMERIZATION; THIN-FILMS; C-60; FABRICATION; NETWORKS; LINKING; GROWTH;
D O I
10.1088/1361-648X/aab0b9
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
On-surface synthesis has rapidly emerged as a most promising approach to prepare functional molecular structures directly on a support surface. Compared to solution synthesis, performing chemical reactions on a surface offers several exciting new options: due to the absence of a solvent, reactions can be envisioned that are otherwise not feasible due to the insolubility of the reaction product. Perhaps even more important, the confinement to a two-dimensional surface might enable reaction pathways that are not accessible otherwise. Consequently, on-surface synthesis has attracted great attention in the last decade, with an impressive number of classical reactions transferred to a surface as well as new reactions demonstrated that have no classical analogue. So far, the majority of the work has been carried out on conducting surfaces. However, when aiming for electronic decoupling of the resulting structures, e.g. for the use in future molecular electronic devices, non-conducting surfaces are highly desired. Here, we review the current status of on-surface reactions demonstrated on the (10.4) surface of the bulk insulator calcite. Besides thermally induced C-C coupling of halogen-substituted aryls, photochemically induced [2 + 2] cycloaddition has been proven possible on this surface. Moreover, experimental evidence exists for coupling of terminal alkynes as well as diacetylene polymerization. While imaging of the resulting structures with dynamic atomic force microscopy provides a direct means of reaction verification, the detailed reaction pathway often remains unclear. Especially in cases where the presence of metal atoms is known to catalyze the corresponding solution chemistry reaction (e.g. in the case of the Ullmann reaction), disclosing the precise reaction pathway is of importance to understand and generalize on-surface reactivity on a bulk insulator surface. To this end, density-functional theory calculations have proven to provide atomic-scale insights that have greatly contributed to unravelling the details of on-surface synthesis on a bulk insulator surface.
引用
收藏
页数:15
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