Gerencia Química, Comisión Nacional de Energía Atómica, Argentina.
Langmuir. 2012 Feb 21;28(7):3583-92. doi: 10.1021/la204854r. Epub 2012 Feb 7.
Rational construction of interfaces based on multicomponent responsive systems in which molecular transport is mediated by structures of nanoscale dimensions has become a very fertile research area in biomimetic supramolecular chemistry. Herein, we describe the creation of hybrid mesostructured interfaces with reversible gate-like transport properties that can be controlled by chemical inputs, such as protons or calcium ions. This was accomplished by taking advantage of the surface-initiated polymerization of 2-(methacryloyloxy)ethyl phosphate (MEP) monomer units into and onto mesoporous silica thin films. In this way, phosphate-bearing polymer brushes were used as "gatekeepers" located not only on the outer surface of mesoporous thin films but also in the inner environment of the porous scaffold. Pore-confined PMEP brushes respond to the external triggering chemical signals not only by altering their physicochemical properties but also by switching the transport properties of the mesoporous film. The ion-gate response/operation was based on the protonation and/or chelation of phosphate monomer units in which the polymer brush works as an off-on switch in response to the presence of protons or Ca(2+) ions. The hybrid meso-architectured interface and their functional features were studied by a combination of experimental techniques including ellipso-porosimetry, cyclic voltammetry, X-ray reflectivity, grazing incidence small-angle X-ray scattering, X-ray photoelectron spectroscopy, and in situ atomic force microscopy. In this context, we believe that the integration of stimuli-responsive polymer brushes into nanoscopic supramolecular architectures would provide new routes toward multifunctional biomimetic nanosystems displaying transport properties similar to those encountered in biological ligand-gated ion channels.
基于多组分响应体系的界面的合理构建,其中分子传输是由纳米尺寸的结构介导的,已经成为仿生超分子化学中一个非常有活力的研究领域。在此,我们描述了具有可逆门控传输特性的混合介孔界面的构建,这种界面可以通过化学输入(如质子或钙离子)进行控制。这是通过利用 2-(甲基丙烯酰氧基)乙基磷酸酯(MEP)单体单元在介孔二氧化硅薄膜内外表面上的引发聚合来实现的。这样,含磷聚合物刷不仅位于介孔薄膜的外表面,而且位于多孔支架的内部环境中,作为“门卫”。孔限制的 PMEP 刷不仅通过改变其物理化学性质,而且通过切换介孔薄膜的传输性质来响应外部触发化学信号。离子门的响应/操作基于磷酸单体单元的质子化和/或螯合,其中聚合物刷作为响应质子或 Ca(2+)离子存在的开/关开关。通过包括椭圆孔隙率测定法、循环伏安法、X 射线反射率、掠入射小角 X 射线散射、X 射线光电子能谱和原位原子力显微镜在内的一系列实验技术对混合介孔结构界面及其功能特征进行了研究。在这种情况下,我们相信将响应性聚合物刷整合到纳米尺度的超分子结构中,将为具有类似于生物配体门控离子通道的传输性质的多功能仿生纳米系统提供新途径。