4.8 Article

Dynamics of Spatially Confined Bisphenol A Trimers in a Unimolecular Network on Ag(111)

期刊

NANO LETTERS
卷 16, 期 3, 页码 1884-1889

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.5b05026

关键词

Self-assembly; rotor arrays; scanning tunneling microscopy; dispersion-corrected density-functional tight-binding; silver surface

资金

  1. ERC Advanced Grant MolArt [247299]
  2. Marie Curie Intra-European Fellowship (project NASUMECA) [274842]
  3. Marie Curie International Incoming Fellowship (Project NANOULOP) [302157]
  4. Alexander von Humboldt Foundation
  5. Helmholtz-Zentrum Berlin (HZB)

向作者/读者索取更多资源

Bisphenol A (BPA) aggregates on Ag(111) shows a polymorphism between two supramolecular motifs leading to formation of distinct networks depending on thermal energy. With rising temperature a dimeric pairing scheme reversibly converts into a trimeric motif, which forms a hexagonal superstructure with complex dynamic characteristics. The trimeric arrangements notably organize spontaneously into a self-assembled one-component array with supramolecular BPA rotors embedded in a two-dimensional stator sublattice. By varying the temperature, the speed of the rotors can be controlled as monitored by direct visualization. A combination of scanning tunneling microscopy and dispersion corrected density-functional tight-binding (DFTB-vdW(surf)) based molecular modeling reveals the exact atomistic position of each molecule within the assembly as well as the driving force for the formation of the supramolecular rotors.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据