期刊
INORGANIC CHEMISTRY
卷 54, 期 5, 页码 2284-2299出版社
AMER CHEMICAL SOC
DOI: 10.1021/ic5028916
关键词
-
资金
- Universite de Bordeaux
- Centre National de la Recherche Scientifique (CNRS)
- Agence Nationale pour la Recherche (ANR)
- L'Oreal
The design of redox-robust polymers is called for in view of interactions with nanoparticles and surfaces toward applications in nanonetwork design, sensing, and catalysis. Redox-robust triazolylbiferrocenyl (trzBiFc) polymers have been synthesized with the organometallic group in the side chain by ring-opening metathesis polymerization using Grubbs-III catalyst or radical polymerization and with the organometallic group in the main chain by Cu(I) azide alkyne cycloaddition (CuAAC) catalyzed by [Cu(I)(hexabenzyltren)]Br. Oxidation of the trzBiFc polymers with ferricenium hexafluorophosphate yields the stable 35-electron class-II mixed-valent biferrocenium polymer. Oxidation of these polymers with Au-III or Ag-I gives nanosnake-shaped networks (observed by transmission electron microscopy and atomic force microscopy) of this mixed-valent (FeFeIII)-Fe-II polymer with encapsulated metal nanoparticles (NPs) when the organoiron group is located on the side chain. The factors that are suggested to be synergistically responsible for the NP stabilization and network formation are the polymer bulk, the trz coordination, the nearby cationic charge of trzBiFc, and the inter-BiFc distance. For instance, reduction of such an oxidized trzBiFc-AuNP polymer to the neutral trzBiFc-AuNP polymer with NaBH4 destroys the network, and the product flocculates. The polymers easily provide modified electrodes that sense, via the oxidized (FeFeIII)-Fe-II and (FeFeIII)-Fe-III polymer states, respectively, ATP(2) via the outer ferrocenyl units of the polymer and Pd-II via the inner Fc units; this recognition works well in dichloromethane, but also to a lesser extent in water with NaCl as the electrolyte.
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。
推荐
暂无数据