Vilanova Neus, De Feijter Isja, Voets Ilja K
Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology; Institute for Complex Molecular Systems, Eindhoven University of Technology.
Laboratory of Macromolecular and Organic Chemistry, Eindhoven University of Technology; Laboratory of Chemical Biology, Eindhoven University of Technology; Institute for Complex Molecular Systems, Eindhoven University of Technology.
J Vis Exp. 2016 Apr 22(110):53934. doi: 10.3791/53934.
Control over colloidal assembly is of utmost importance for the development of functional colloidal materials with tailored structural and mechanical properties for applications in photonics, drug delivery and coating technology. Here we present a new family of colloidal building blocks, coined supramolecular colloids, whose self-assembly is controlled through surface-functionalization with a benzene-1,3,5-tricarboxamide (BTA) derived supramolecular moiety. Such BTAs interact via directional, strong, yet reversible hydrogen-bonds with other identical BTAs. Herein, a protocol is presented that describes how to couple these BTAs to colloids and how to quantify the number of coupling sites, which determines the multivalency of the supramolecular colloids. Light scattering measurements show that the refractive index of the colloids is almost matched with that of the solvent, which strongly reduces the van der Waals forces between the colloids. Before photo-activation, the colloids remain well dispersed, as the BTAs are equipped with a photo-labile group that blocks the formation of hydrogen-bonds. Controlled deprotection with UV-light activates the short-range hydrogen-bonds between the BTAs, which triggers the colloidal self-assembly. The evolution from the dispersed state to the clustered state is monitored by confocal microscopy. These results are further quantified by image analysis with simple routines using ImageJ and Matlab. This merger of supramolecular chemistry and colloidal science offers a direct route towards light- and thermo-responsive colloidal assembly encoded in the surface-grafted monolayer.
对于开发具有定制结构和机械性能的功能性胶体材料以应用于光子学、药物递送和涂层技术而言,控制胶体组装至关重要。在此,我们展示了一类新的胶体构建单元,即超分子胶体,其自组装通过用源自苯 -1,3,5- 三甲酰胺(BTA)的超分子部分进行表面功能化来控制。此类BTA通过定向、强且可逆的氢键与其他相同的BTA相互作用。本文介绍了一种方案,该方案描述了如何将这些BTA与胶体偶联以及如何量化偶联位点的数量,偶联位点数量决定了超分子胶体的多价性。光散射测量表明,胶体的折射率几乎与溶剂的折射率匹配,这极大地降低了胶体之间的范德华力。在光激活之前,胶体保持良好分散状态,因为BTA配备了一个光不稳定基团,该基团会阻止氢键的形成。用紫外光进行可控脱保护会激活BTA之间的短程氢键,从而引发胶体自组装。通过共聚焦显微镜监测从分散状态到聚集状态的演变。使用ImageJ和Matlab通过简单程序进行图像分析进一步量化了这些结果。超分子化学与胶体科学的这种融合为在表面接枝单分子层中编码的光响应和热响应胶体组装提供了一条直接途径。