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首页> 外文期刊>Journal of the American Chemical Society >Epitaxial Growth of γ-Cyclodextrin-Containing Metal-Organic Frameworks Based on a Host-Guest Strategy
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Epitaxial Growth of γ-Cyclodextrin-Containing Metal-Organic Frameworks Based on a Host-Guest Strategy

机译:基于宿主-客座策略的含γ-环糊精的金属有机骨架的外延生长

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摘要

A class of metal organic frameworks (MOFs)-namely CD-MOFs obtained from natural products has been grown in an epitaxial fashion as films on the surfaces of glass substrates, which are modified with self-assembled monolayers (SAMs) of gamma-cyclodextrin (gamma-CD) molecules. The SAMs are created by host guest complexation of gamma-CD molecules with surface-functionalized pyrene units. The CD-MOF films have continuous polycrystalline morphology with a structurally out-of plane (c-axial) orientation, covering an area of several square millimeters, with a thickness of similar to 2 mu m. Furthermore, this versatile host-guest strategy has been applied successfully in the growth of CD-MOFs as the shell on the curved surface of microparticles as well as in the integration of CD-MOF films into electrochemical devices for sensing carbon dioxide. In striking contrast to the control devices prepared from CD-MOF crystalline powders, these CD-MOF film-based devices display an enhancement in proton conductance of up to 300-fold. In addition, the CD-MOF film-based device exhibits more rapid and highly reversible CO2-sensing cycles under ambient conditions, with a 50-fold decrease in conductivity upon exposure to CO2 for 3 s which is recovered within 10 s upon re-exposure to air.
机译:一类金属有机骨架(MOF),即从天然产物中获得的CD-MOF,已外延生长为玻璃基板表面上的薄膜,并通过γ-环糊精的自组装单层(SAM)进行了修饰( γ-CD)分子。 SAM是由宿主CD-γ分子与表面官能化的units单元进行客体络合而形成的。 CD-MOF膜具有连续的多晶形态,其结构在平面外(c轴)取向,覆盖几平方毫米的面积,厚度近似于2微米。此外,这种通用的主客体策略已成功地应用于作为微粒弯曲表面上的壳的CD-MOF的生长,以及将CD-MOF薄膜集成到用于感应二氧化碳的电化学装置中。与由CD-MOF晶体粉末制成的控制装置形成鲜明对比的是,这些基于CD-MOF薄膜的装置显示出质子传导性的提高高达300倍。此外,基于CD-MOF薄膜的器件在环境条件下表现出更快速和高度可逆的CO2感测周期,在暴露于CO2 3s后电导率降低50倍,在再次暴露后10s内可恢复播出。

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  • 来源
    《Journal of the American Chemical Society》 |2018年第36期|11402-11407|共6页
  • 作者单位

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Tianjin Univ, Inst Mol Design & Synth, 92 Weijin Rd, Tianjin 300072, Peoples R China;

    PanaceaNano Inc, 2265 East Foothill Blvd, Pasadena, CA 91107 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

    Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA;

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