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首页> 外文期刊>ChemElectroChem >Surface Patterning of Biomolecules Using Click Chemistry and Light-Activated Electrochemistry to Locally Generate Cu(I)
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Surface Patterning of Biomolecules Using Click Chemistry and Light-Activated Electrochemistry to Locally Generate Cu(I)

机译:使用点击化学和光激活电化学来局部产生Cu(i)表面图案化生物分子的表面图案化

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摘要

Here we report a light-assisted variant of click chemistry suitable for chemical patterning of semiconducting surfaces. Using a visible light beam to illuminate desired locations of an electrode surface, localized electrogeneration of the Cu(I) click catalyst was achieved. It was demonstrated that surface click reactions were correlated with a user-defined 2D light pattern projected on a silicon photoelectrode. This new process is mask-free and parallel, i. e., separate discrete regions of a semiconducting surface can be simultaneously reacted with a range of functional molecules. The covalent patterning of azido-poly (ethylene glycol) molecules (PEG) over alkyne-functionalized electrodes was employed as a proof-of-principle. By modulating the exposed chemical group of the clicked azido-PEGs, the adhesion of antibodies and cells was further possible with spatial control. The use of structured light, instead of physical masks, drastically reduces patterning time to a couple of hours.
机译:在这里,我们报告了一个适用于半导体表面的化学图案化的咔哒化化学的光辅助变体。 使用可见光光束照射电极表面的所需位置,实现了Cu(I)咔哒催化剂的局部电流。 据证明,表面咔哒反应与突出在硅光电极上突出的用户定义的2D光图案相关。 这一新进程是无掩盖和平行的,i。 即,半导体表面的单独离散区域可以同时与一系列功能分子反应。 将Azido-poly(乙二醇)分子(PEG)通过炔烃官能化电极的共价图案化作为原则验证。 通过调节点击的Azido-PEG的暴露的化学组,通过空间控制,还可以进一步实现抗体和细胞的粘附性。 使用结构光,而不是物理掩模,急剧减少了图案时间到几个小时。

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