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Synthesis and characterization of multidimensional supramolecular networks supported by multitopic tris(pyrazolyl)methane ligands.

机译:多主题三(吡唑基)甲烷配体支持的多维超分子网络的合成与表征。

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摘要

The development and synthesis of several new multitopic ligands based on tris(pyrazolyl)methane donor units and their use in the synthesis of multidimensional supramolecular architectures is discussed. The strategy here consist of using non-covalent forces such as weak hydrogen bonds, C--H ··· pi interactions or pi - pi stacking to influence the outcome of the covalently bonded networks. Based on this approach, a non-covalent strategy for the assembly of covalent networks was established. The same non-covalent driving forces can be used to induce a specific crystal packing of discrete cage-like supermolecules.;The robustness of non-covalent forces within this system will also be addressed. A combination of X-ray crystallography, IR spectroscopy, DFT calculations and ES/MS studies have been used to investigate the solid state and solution properties of silver(I) complexes formed from closely related semi-rigid, multitopic ligands, one of which is tetratopic and the other two bitopic analogs that can each be viewed as possessing half of the bonding properties of the first. The covalent and supramolecular structures of the silver(I) complexes based on this type of ligands are surprisingly similar, both being organized in a comparable architecture by the same non-covalent forces.
机译:讨论了基于三(吡唑基)甲烷供体单元的几种新型多位配体的开发和合成及其在多维超分子体系结构合成中的应用。这里的策略包括使用非共价力,例如弱氢键,CH--π相互作用或π-π堆积来影响共价键合网络的结果。基于这种方法,建立了用于共价网络组装的非共价策略。相同的非共价驱动力可用于诱导离散的笼状超分子的特定晶体堆积。;还将解决该系统中非共价力的鲁棒性。 X射线晶体学,红外光谱,DFT计算和ES / MS研究相结合,已用于研究由紧密相关的半刚性多位配体形成的银(I)配合物的固态和溶液性质,其中之一是可以将四位和其他两个双位类似物视为具有第一个键合特性的一半。基于这种类型的配体的银(I)配合物的共价和超分子结构令人惊讶地相似,两者均以相同的非共价力以可比的结构组织。

著录项

  • 作者

    Semeniuc, Radu Florin.;

  • 作者单位

    University of South Carolina.;

  • 授予单位 University of South Carolina.;
  • 学科 Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 218 p.
  • 总页数 218
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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