4.8 Article

Unconventional Single-Molecule Conductance Behavior for a New Heterocyclic Anchoring Group: Pyrazolyl

期刊

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 9, 期 18, 页码 5364-5372

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.8b02051

关键词

-

资金

  1. Ministerio de Economia y Competitividad from Spain [MAT2016-78257-R]
  2. fondos FEDER [CTQ2015-70174-P]
  3. project Hierarchical Self Assembly of Polymeric Soft Systems, SASSYPOL, from the seventh Framework Programme (CEE) [607602]
  4. DGA/Fondos FEDER (construyendo Europa desde Aragon) [E31_17R, E47_17R]
  5. EPSRC QuEEN programme [EP/N017188/1]
  6. UK EPSRC [EP/M014452/1, EP/P027156/1, EP/N03337X/1]
  7. European Commission [767187 - QuIET]
  8. Iraqi Ministry of Higher Education [SL-20]
  9. Tikrit University (Iraq)
  10. EPSRC [EP/M005046/1, EP/M014169/1, EP/M029522/1]
  11. EPSRC [EP/M014169/1, EP/M005046/1, EP/M014452/1, EP/M029522/1, EP/N03337X/1, EP/P027156/1, EP/N017188/1] Funding Source: UKRI

向作者/读者索取更多资源

Electrical conductance across a molecular junction is strongly determined by the anchoring group of the molecule. Here we highlight the unusual behavior of 1,4-bis(1H-pyrazol-4-ylethynyl)benzene that exhibits unconventional junction current versus junction-stretching distance curves, which are peak-shaped and feature two conducting states of 2.3 X 10(-4) G(0) and 3.4 X 10(-4) G(0). A combination of theory and experiments is used to understand the conductance of single-molecule junctions featuring this new anchoring group, i.e., pyrazolyl. These results demonstrate that the pyrazolyl moiety changes its protonation state and contact binding during junction evolution and that it also binds in either end-on or facial geometries with gold contacts. The pyrazolyl moiety holds general interest as a contacting group, because this linkage leads to a strong double anchoring of the molecule to the gold electrode, resulting in enhanced conductance values.

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