首页> 外文期刊>Journal of the American Chemical Society >Crystal Transformation from the Incorporation of Coordinate Bonds into a Hydrogen-Bonded Network Yields Robust Free-Standing Supramolecular Membranes
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Crystal Transformation from the Incorporation of Coordinate Bonds into a Hydrogen-Bonded Network Yields Robust Free-Standing Supramolecular Membranes

机译:从配位键结合到氢键网络中的晶体转变产生了坚固的自由站立的超分子膜。

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摘要

In this work, we report on the synthesis of a freestanding, macroscopic robust supramolecular membrane by introducing silver—nitrogen coordinate bonding into preorgan-ized, supramolecular hydrogen-bonded cyanuric acid-melamine (CAM) crystals. With the assistance of ammonia, silver ions competitively replace two of the three hydrogen atoms from cyanuric acid resulting in the transformation from short CAM nanorods to long CAM-Ag nanofibers (length over 1000 μm), accompanied by tautomerization of cyanuric acid. The single crystal structure of the CAM-Ag nanofibers is solved in the space group P1, with the asymmetric unit containing eight silver atoms, four melamine and four cyanuric acid molecules, which generate 1D coordination polymer chains consisting of alternating melamine and dianionic cyanurate ligands linked via silver—nitrogen bonds. The presence of interchain hydrogen bonds results in the expansion of the supramolecular network into undulating 2D sheets, which then stack into a 3D network via a series of intersheet hydrogen bonds and π—π interactions. Significantly, the CAM-Ag nanofibers spontaneously assemble into a free-standing membrane, with lateral size up to square centimeters and thickness of 30 μm. The membrane shows high flexibility and mechanical strength, owing to the improved flexibility of the CAM-Ag nanofibers with bonded chain structure, and can be reversibly and repeatedly bent over 90 degrees. Remarkably, the CAM-Ag membrane demonstrates distinct optical transmittance being shortwave IR transmissive but impenetrable to UV and visible light.
机译:在这项工作中,我们报告了通过将银-氮配位键引入到预组织的,超分子氢键合的氰尿酸-三聚氰胺(CAM)晶体中,合成了一种独立的,宏观的,坚固的超分子膜。在氨的帮助下,银离子竞争性地取代了氰尿酸中的三个氢原子中的两个,从而导致了短CAM纳米棒向长CAM-Ag纳米纤维(长度超过1000μm)的转变,并伴随着氰尿酸的互变异构化。 CAM-Ag纳米纤维的单晶结构在空间群P1中求解,其不对称单元包含八个银原子,四个三聚氰胺和四个氰尿酸分子,它们生成一维配位聚合物链,该链由交替的三聚氰胺和二价氰尿酸酯配体连接而成通过银-氮键。链间氢键的存在导致超分子网络扩展为起伏的2D片,然后通过一系列片间氢键和π-π相互作用堆叠为3D网络。值得注意的是,CAM-Ag纳米纤维自发地组装成独立的膜,其横向尺寸最大为平方厘米,厚度为30μm。由于具有键合链结构的CAM-Ag纳米纤维的挠性得到改善,该膜具有很高的挠性和机械强度,并且可以可逆地重复弯曲90度。值得注意的是,CAM-Ag膜显示出独特的光学透射率,可以短波IR透射,但不能穿透UV和可见光。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2020年第1期|479-486|共8页
  • 作者单位

    School of Chemistry Physics and Mechanical Engineering Science and Engineering Faculty Queensland University of Technology Brisbane QLD 4001 Australia;

    Insitute for Future Environments Science and Engineering Faculty Queensland University of Technology Brisbane QLD 4001 Australia;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 05:17:05

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