Ito Takashi, Higgins Daniel A
Department of Chemistry, Kansas State University, 213 CBC Building, Manhattan, KS 66506-0401, USA.
Chem Rec. 2021 Jun;21(6):1417-1429. doi: 10.1002/tcr.202000173. Epub 2021 Feb 3.
Many analytical methods employ self-assembled nanostructured materials as chemical recognition media. Molecular permeation through these materials exhibits unique selectivity owing to nanoconfinement-induced enhancement of permeant-nanostructure interactions. This Personal Account introduces our efforts to investigate the detailed dynamics of single or a small number of molecules in nanostructured materials. We developed new experimental and analysis approaches built upon laser-based fluorescence microscopy to measure the detailed translational and orientational dynamics of molecules diffusing in horizontally-oriented, cylindrical nanostructures, including surfactant micelles, silica mesopores, block copolymer microdomains, and bolaamphiphile-based organic nanotubes. Our studies clarified nanoscale details on the structural/chemical heterogeneity of the nanostructures, and their impacts on molecular mass transport dynamics.
许多分析方法采用自组装纳米结构材料作为化学识别介质。由于纳米限域作用增强了渗透物与纳米结构之间的相互作用,分子透过这些材料表现出独特的选择性。这篇个人述评介绍了我们为研究纳米结构材料中单个或少量分子的详细动力学所做的努力。我们基于激光荧光显微镜开发了新的实验和分析方法,以测量在水平取向的圆柱形纳米结构(包括表面活性剂胶束、二氧化硅介孔、嵌段共聚物微区和基于双两性离子的有机纳米管)中扩散的分子的详细平移和取向动力学。我们的研究阐明了纳米结构在结构/化学异质性方面的纳米级细节,以及它们对分子质量传输动力学的影响。