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Structural Influences of Noncovalent Interactions in the Gas Phase

机译:气相中非共价相互作用的结构影响

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摘要

The physical properties of molecules in solution, such as basicity and structure, depend on the cooperation and competition of noncovalent intra- and intermolecular interactions. Studying these interactions in the condensed phase is made difficult by the presence of competing influences from counterions and impurities. In the gas phase, however, specific ions, ion complexes and hydration states can be isolated and studied by Fourier transform mass spectrometry coupled with infrared (IR) laser spectroscopy. Using these two techniques, it is possible to isolate specific ions before inducing dissociation via absorption of IR photons. The extent of absorption at a given wavelength correlates to the relative abundance of product ions produced via dissociation, which can be measured using mass spectrometry. The absorption of IR photons only occurs at specific wavelengths depending on which functional groups are present and how their vibrational modes are influenced by interactions such as hydrogen bonding. Structural information is obtained from these spectra by interpreting the presence of certain bands and their frequencies. In addition, information can also be obtained by comparing the spectra from ions of interest to the spectra of reference ions, with known structures, or the simulated spectra of computed geometries. These types of studies provide valuable insight into how noncovalent interactions govern the structure of biomolecules and hydrogen-bonded networks. This dissertation reports experiments utilizing IR spectroscopy to study how waterion interactions can affect both the structure of an ion solvated by an aqueous nanodrop as well as the hydrogen-bonding network of the nanodrop itself. In addition, the structural effects of ion-peptide interactions, which are relevant to understanding how ions influence biological processes, are also investigated. (Abstract shortened by ProQuest.).
机译:溶液中分子的物理性质,例如碱度和结构,取决于非共价分子内和分子间相互作用的协作和竞争。由于抗衡离子和杂质的竞争影响的存在,很难研究缩合相中的这些相互作用。然而,在气相中,特定离子,离子络合物和水合状态可以通过傅里叶变换质谱结合红外(IR)激光光谱法进行分离和研究。使用这两种技术,可以在通过吸收红外光子而引起解离之前分离出特定的离子。在给定波长下的吸收程度与通过解离产生的产物离子的相对丰度相关,可以使用质谱法对其进行测量。 IR光子的吸收仅在特定波长下发生,具体取决于存在哪些官能团以及它们的振动模式如何受到相互作用(例如氢键)的影响。通过解释某些频段的存在及其频率,可以从这些光谱中获得结构信息。此外,还可以通过将目标离子的光谱与参考离子的光谱与已知结构进行比较,或者将计算的几何图形的模拟光谱进行比较,从而获得信息。这些类型的研究为非共价相互作用如何控制生物分子和氢键网络的结构提供了宝贵的见识。这篇论文报道了利用红外光谱的实验,研究水离子相互作用如何影响被水纳米滴溶剂化的离子的结构以及纳米滴本身的氢键网络。此外,还研究了离子-肽相互作用的结构效应,该效应与理解离子如何影响生物过程有关。 (摘要由ProQuest缩短。)。

著录项

  • 作者

    Chang, Terrence.;

  • 作者单位

    University of California, Berkeley.;

  • 授予单位 University of California, Berkeley.;
  • 学科 Chemistry.;Physical chemistry.;Analytical chemistry.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 109 p.
  • 总页数 109
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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