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Molecular tectonics: Supramolecular two-dimensional nanopatterning of surfaces by self-assembly.

机译:分子构造:通过自组装对表面进行超分子二维纳米构图。

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摘要

In recent years, molecular tectonics has been employed as an efficient strategy in the construction of supramolecular architectures in three dimensions (3D). The building blocks used in this strategy, which have been called tectons, have structures with well-defined geometries and multiple functional groups that control intermolecular association by forming directional interactions, such as hydrogen bonds. A new opportunity exists to adopt this strategy to create well-defined 2D molecular networks on the surfaces of various substrates, such as graphite. In this dissertation, a series of new tectons have been purposefully designed and synthesized for nanopatterning surfaces, and their adsorption on highly oriented pyrolytic graphite (HOPG) has been thoroughly examined by scanning tunneling microscopy (STM).;Specifically, the tectons investigated herein incorporate systematic changes of molecular length, cores, functional groups, and molecular geometries. The basic cores, which are aromatic systems such as benzene, naphthalene, and anthracene, are grafted to conjugated linkers, including acetylene and arylacetylene, and to various functional groups with different abilities to engage in intermolecular interactions, including diaminotriazine groups, carboxylic acids, and related substituents. The observation of diverse nanopatterns has led to a deeper understanding of (1) how the basic backbone interacts with surfaces, (2) how the functional groups modify the behavior of the backbone, and (3) how the formation of interadsorbate interactions further influences adsorption.;Our work demonstrates that rational 2D and 3D molecular assembly can be achieved and analyzed by an integrated approach using the tools of STM, X-ray diffraction, computation, and molecular synthesis. Furthermore, our work confirms that molecules with well-defined shapes and multiple sites that engage in strong directional interactions are a consistently productive source of new materials with properties not previously observed.;Key words: Molecular tectonics, 2D nanopatterning, scanning tunneling microscopy (STM), self-assembly.;To understand the details of molecular adsorption, multiple methods of characterization and analysis have been used in this work, including (1) direct examination of adsorption by STM, (2) systematic alteration of the structure of the adsorbate to reveal how the self-assembled 2D nanopatterns changes, (3) comparison of the observed 2D nanopatterns with those seen in 3D structures by X-ray crystallography, and 4) theoretical calculations to help disclose the origin of molecular adsorption.
机译:近年来,分子构造已被用作在三维(3D)上构建超分子体系的有效策略。此策略中使用的构造块(称为构造子)具有结构明确的几何结构和多个官能团,这些官能团通过形成方向性相互作用(例如氢键)控制分子间的缔合。存在采用这种策略的新机会,以便在各种基底(例如石墨)的表面上创建定义明确的2D分子网络。本论文针对纳米图案表面,设计并合成了一系列新的构造,并通过扫描隧道显微镜(STM)对它们在高取向热解石墨(HOPG)上的吸附进行了全面研究。分子长度,核心,官能团和分子几何结构的系统变化。基本核心是芳香系统,例如苯,萘和蒽,被接枝到共轭接头(包括乙炔和芳基乙炔)上,并接枝到具有不同能力的分子间相互作用的各种官能团上,包括二氨基三嗪基,羧酸和相关的取代基。对各种纳米图案的观察已导致对以下方面的更深入了解:(1)基本骨架如何与表面相互作用;(2)官能团如何修饰骨架的行为;(3)相互吸附物相互作用的形成如何进一步影响吸附我们的工作表明,可以使用STM,X射线衍射,计算和分子合成工具通过集成方法实现合理的2D和3D分子组装和分析。此外,我们的工作证实具有清晰形状和具有强方向相互作用的多个位点的分子是新材料的持续生产性来源,其新特性以前从未观察到。;关键词:分子构造,二维纳米图案,扫描隧道显微镜(STM)为了了解分子吸附的细节,这项工作中使用了多种表征和分析方法,包括(1)通过STM直接检查吸附,(2)系统改变吸附物的结构为了揭示自组装2D纳米图案的变化,(3)将观察到的2D纳米图案与通过X射线晶体学在3D结构中看到的2D纳米图案进行比较,以及4)理论计算以帮助揭示分子吸附的起源。

著录项

  • 作者

    Zhou, Hui.;

  • 作者单位

    Universite de Montreal (Canada).;

  • 授予单位 Universite de Montreal (Canada).;
  • 学科 Chemistry Physical.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 316 p.
  • 总页数 316
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
  • 关键词

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