2000年
Characterization of novel redox-active triruthenium(III) complexes with a disulfide alkyl ligand. Anion-dependent redox behaviour of monolayer assemblies on gold
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
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- 巻
- 号
- 16
- 開始ページ
- 2693
- 終了ページ
- 2702
- 記述言語
- 英語
- 掲載種別
- 書評論文,書評,文献紹介等
- DOI
- 10.1039/b002105i
- 出版者・発行元
- ROYAL SOC CHEMISTRY
New oxo-centred acetate-bridged triruthenium(III) complexes with a long alkyl-chain disulfide ligand, (NC5H4)CH2NHC(O)(CH2)(n)SS(CH2)(n)C(O)NHCH2(C5H4N) (C5H4N represents a 4-pyridyl residue, n=10; abbreviated as C10PY), have been prepared as a redox-active metal cluster adsorbate on gold electrodes: [Ru-3(O)(CH3CO2)(6)(mpy)(2)(C10PY)]ClO4 5a (mpy=4-methylpyridine), [Ru-3(O)(CH3CO2)(6)(mpy)(2)(C10PY)]CF3SO3 5b. The preparation, spectroscopic and electrochemical properties of 5a,5b are presented and are compared with those of triruthenium(III) analogues of a shorter alkyl-chain disulfide ligand (n=2; abbreviated as C2PY), e.g. [Ru-3(O)(CH3CO2)(6)(mpy)(2)(C2PY)]ClO4 3a and [Ru-3(O)(CH3CO2)(6)(MeIm)(2)(C2PY)]ClO4 4a (MeIm=1-methylimidazole). Characterization of all the compounds was accomplished using H-1 and H-1-H-1 COSY NMR, UV-vis and infrared spectroscopy, elemental analysis, fast-atom bombardment (FAB) mass spectrometry and cyclic voltammetry. Compounds 3a, 4a and 5a,5b in 0.1 M [n-Bu4N]PF6-CH3CN exhibit three {Ru-3(O)} cluster core-based one-electron redox waves which are all reversible in the applied potential range between +1.2 and -2.0 V vs. Ag-AgCl. The redox potentials are dependent on the basicity of the terminal ligands (mpy and MeIm), but are insensitive to the length of the methylene chains of the disulfide ligand (C10PY and C2PY). Self-assembly of 5b on a gold electrode results in the formation of electrochemically stable monolayers which exhibit one-electron redox wave corresponding to the Ru-3 redox process III,III,III-II,III,III in aqueous media containing 0.1 M supporting electrolytes. The redox potentials and the shape of the voltammetric waves of the surface-attached triruthenium complexes are found to be largely dependent upon the nature of anions used (ClO4-, CF3SO3-, NO3-, PF6- and SO42-) and also upon the basicity of terminal ligands on the {Ru-3(O)} cluster moiety.
- リンク情報
- ID情報
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- DOI : 10.1039/b002105i
- ISSN : 1472-7773
- CiNii Articles ID : 80011798686
- Web of Science ID : WOS:000088759200008