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使用重氮电化学在碳表面设计稳健的二元膜。

Design of robust binary film onto carbon surface using diazonium electrochemistry.

机构信息

Sciences Chimiques de Rennes (Equipe MaCSE), CNRS, UMR 6226, Université de Rennes 1, Campus de Beaulieu, Bat 10C, 35042 Rennes Cedex, France.

出版信息

Langmuir. 2011 Sep 6;27(17):11222-8. doi: 10.1021/la202250y. Epub 2011 Aug 3.

Abstract

The electroreduction of functionalized aryldiazonium salts combined with a protection-deprotection method was evaluated for the fabrication of organized mixed layers covalently bound onto carbon substrates. The first modification consists of the grafting of a protected 4-((triisopropylsilyl)ethynyl)benzene layer onto the carbon surface on which the introduction of a second functional group is possible without altering the first grafted functional group. After deprotection, we obtained an ultrathin robust layer presenting high densities of both active ethynylbenzene groups (available for "click" chemistry) and the second functional group. The strategy was successfully demonstrated using azidomethylferrocene to react with ethynyl moieties in the binary film by "click" chemistry, and NO(2)-phenyl as the second functional group. Two possible modification pathways with different orderings of the various steps were considered to show the influence and importance of the protection-deprotection process on the final surface obtained. Using mild conditions for the grafting of the second layer maintains a concentration of active ethynyl groups similar to that obtained for a one-component monolayer while achieving a high surface concentration of the second modifier. Considering the wide range of functional aryldiazonium salts that could be electrodeposited onto carbon surfaces and the versatility and specificity of the "click" chemistry, this approach appears very promising for the preparation of mixed layers in well-controlled conditions without altering the reactivity of either functional group.

摘要

通过电还原功能化芳基重氮盐与保护-脱保护方法相结合,评估了在碳基底上制备共价结合的有序混合层的方法。第一种修饰方法包括将受保护的 4-((三异丙基甲硅烷基)乙炔基)苯层接枝到碳表面上,在不改变第一个接枝官能团的情况下,这使引入第二个官能团成为可能。脱保护后,我们得到了一个超薄的坚固层,具有高浓度的活性乙炔基苯基团(可用于“点击”化学)和第二个官能团。该策略使用叠氮甲基二茂铁作为第二个官能团,通过“点击”化学与二元膜中的乙炔基反应,成功地得到了证明。考虑了两种可能的修饰途径,其中各种步骤的顺序不同,以显示保护-脱保护过程对最终表面的影响和重要性。使用温和的条件接枝第二层可以保持与单一组分单层类似的活性乙炔基浓度,同时实现第二个修饰剂的高表面浓度。考虑到可以在碳表面上电沉积的各种功能化芳基重氮盐的广泛范围,以及“点击”化学的多功能性和特异性,这种方法在无需改变任何官能团的反应性的情况下,在可控条件下制备混合层非常有前景。

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