4.7 Article

Electrochemical and infrared spectroscopic study of the self-assembled monolayer of a cyano-bridged dimeric triruthenium complex on gold surface

Journal

JOURNAL OF ELECTROANALYTICAL CHEMISTRY
Volume 714, Issue -, Pages 51-55

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jelechem.2013.12.012

Keywords

Self-assembled monolayer; Bridged cyanide; Oxo-centered triruthenium complexes; Gold surface; In situ infrared spectroscopy

Funding

  1. JSPS KAKENHI from the Ministry of Education, Culture, Sports, Science and Technology of Japan [24550143]
  2. Japan Society for the Promotion of Science [P05123]
  3. Cooperative Research Program of Catalysis Research Center, Hokkaido University [12A0007]
  4. [2107]
  5. [24108701]
  6. [24108730]
  7. Grants-in-Aid for Scientific Research [24108730, 24108701, 26620048, 23350058, 24550143] Funding Source: KAKEN

Ask authors/readers for more resources

A new cyano-bridged dimeric oxo-centered triruthenium complex [{Ru-3(mu(3)-O)(mu-CH3COO)(6)(py)(2)}(mu-CN){Ru-3(mu(3)-O)(mu-CH3COO)(6)(py)(Lpy-ss)}](+) (py = pyridine, Lpy-ss = (C5H4N-CH2NHC(O)(CH2)(4)CH(CH2)(2)SS) ([1](+)) has been prepared, characterized, and confined on an Au(111) surface to form self-assembled monolayers (SAMs) (1/Au). The redox and IR spectroscopic properties observed for the discrete ions are essentially preserved in its SAMs. The molecules of SAMs 1/Au stand up with the cyano groups tilted to the gold surface. The electronic structures of 1/Au in different oxidation states have been studied by in situ infrared spectroscopy monitoring the stretching modes of the cyano group. The extent of cyano-mediated electronic communications between two triruthenium units in the SAMs has been successfully tuned by simply changing the electrolyte solutions from 0.1 M n-Bu4NPF6-CH2Cl2 to aqueous 0.1 M HClO4. (C) 2013 Elsevier B.V. All rights reserved.

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