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脒基阳离子与羧酸根阴离子之间的氢键驱动自组装:分子动力学、核磁共振光谱和单晶X射线衍射联合研究

Hydrogen bond-Driven Self-Assembly between Amidinium Cations and Carboxylate Anions: A Combined Molecular Dynamics, NMR Spectroscopy, and Single Crystal X-ray Diffraction Study.

作者信息

Thomas Michael, Anglim Lagones Thomas, Judd Martyna, Morshedi Mahbod, O'Mara Megan L, White Nicholas G

机构信息

Research School of Chemistry, The Australian National University, Canberra, ACT, 2601, Australia.

出版信息

Chem Asian J. 2017 Jul 4;12(13):1587-1597. doi: 10.1002/asia.201700406. Epub 2017 May 23.

Abstract

A combination of molecular dynamics (MD), NMR spectroscopy, and single crystal X-ray diffraction (SCXRD) techniques was used to probe the self-assembly of para- and meta-bis(amidinium) compounds with para-, meta-, and ortho-dicarboxylates. Good concordance was observed between the MD and experimental results. In DMSO solution, the systems form several rapidly exchanging assemblies, in part because a range of hydrogen bonding interactions is possible between the amidinium and carboxylate moieties. Upon crystallization, the majority of the systems form 1D supramolecular polymers, which are held together by short N-H⋅⋅⋅O hydrogen bonds.

摘要

结合分子动力学(MD)、核磁共振光谱(NMR)和单晶X射线衍射(SCXRD)技术,研究了对苯二甲酸、间苯二甲酸和邻苯二甲酸与对双脒基化合物、间双脒基化合物和邻双脒基化合物的自组装。MD模拟结果与实验结果具有良好的一致性。在二甲基亚砜(DMSO)溶液中,这些体系形成了几种快速交换的聚集体,部分原因是脒基和羧基部分之间可能存在一系列氢键相互作用。结晶后,大多数体系形成一维超分子聚合物,这些聚合物通过短的N-H⋅⋅⋅O氢键结合在一起。

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