首页> 外文期刊>ACS applied materials & interfaces >A Copper(II)-Paddlewheel Metal-Organic Framework with Exceptional Hydrolytic Stability and Selective Adsorption and Detection Ability of Aniline in Water
【24h】

A Copper(II)-Paddlewheel Metal-Organic Framework with Exceptional Hydrolytic Stability and Selective Adsorption and Detection Ability of Aniline in Water

机译:铜(II) - 覆盖金属 - 有机骨架,具有卓越的水解稳定性和苯胺在水中的选择性吸附和检测能力

获取原文
获取原文并翻译 | 示例
           

摘要

Copper(II)-paddlewheel-based metal-organic frameworks (CP-MOFs) represent a unique subclass of MOFs with highly predictable porous structures, facile syntheses, and functional open metal sites. However, the lack of high hydrolytic stability is an obstacle for CP-MOFs in many practical applications. In this work, we report a new CP-MOF, [Cu-4(tdhb)] (BUT-155), which is constructed from a judiciously designed carboxylate ligand with high coordination connectivity (octatopic), abundant hydrophobic substituents (six methyl groups), and substituent constrained geometry (tetrahedral backbone), tdhb(8-) [H(8)tdhb = 3,3',5,5'-tetralcis (3,5-dicarboxyphenyl)-2,2',4,4',6,6'-hexamethylbiphenyl)]. BUT-155 shows high porosity with a Brunauer-Emmett-Teller surface area of 2070 m(2)/g. Quite interestingly, this CP-MOF retains its structural integrity after being treated in water for 10 days at room temperature or in boiling water for 24 h. To the best of our knowledge, BUT-15.5 represents the first CP-MOF that is demonstrated to retain its structural integrity in boiling water. The high hydrolytic stability of BUT-155 allowed us to carry out adsorption studies of water vapor and aqueous organic pollutants on it. Water-vapor adsorption reveals a sigmoidal isotherm and a high uptake (46.7 wt %), which is highly reversible and regenerable. In addition, because of the availability of soft-acid-type open Cu(II) sites, BUT-155 shows a high performance for selective adsorption of soft-base-type aniline over water or phenol, and a naked-eye detectable color change for the MOF sample accompanies this. The adsorption selectivity and high adsorption capacity of aniline in BUT-155 are also well-interpreted by single-crystal structures of the water- and aniline-included phases of BUT-15.5.
机译:铜(II) - 基于覆铜金属 - 有机框架(CP-MOF)代表MOF的独特亚类,具有高可预测的多孔结构,容易合成和功能开放金属位点。然而,缺乏高水解稳定性是许多实际应用中CP-MOF的障碍。在这项工作中,我们报告了一种新的CP-MOF [Cu-4(TDHB)](But-155),其由具有高配位连接(缩短),丰富的疏水取代基(六个甲基)的明智设计的羧酸羧酸盐配体构成。 ),取代的约束几何形状(四面体骨架),TDHB(8-)[H(8)TDHB = 3,3',5,5'-Tetralcis(3,5-二羰基苯基)-2,2',4,4 ',6,6'-六甲基哌苯基)]。 But-155显示出高孔隙率,Brunauer-Emmett-extreser面积为2070m(2)/ g。非常有趣的是,这种CP-MOF在室温或沸水中在水中处理10天后保持其结构完整性,或24小时。据我们所知,但是-15.5代表了第一批CP-MOF,以证明在沸水中保持其结构完整性。 But-155的高水解稳定性使我们能够对其进行水蒸气和水性有机污染物的吸附研究。水蒸气吸附揭示了一种六样动物等温线和高吸收(46.7wt%),其高度可逆和可再生。此外,由于软酸型开放Cu(II)位点的可用性,但-155显示了在水或苯酚上选择性吸附软基酸苯胺的高性能,以及裸眼可检测的颜色变化对于MOF样品伴随着这个。在-155中的苯胺中的吸附选择性和高吸附能力也是通过除-15.5的水和苯胺的阶段的单晶结构进行良好解释。

著录项

  • 来源
    《ACS applied materials & interfaces》 |2017年第32期|共9页
  • 作者单位

    Beijing Univ Technol Coll Environm &

    Energy Engn Beijing Key Lab Green Catalysis &

    Separat Beijing 100124 Peoples R China;

    Beijing Univ Technol Coll Environm &

    Energy Engn Beijing Key Lab Green Catalysis &

    Separat Beijing 100124 Peoples R China;

    Beijing Univ Technol Coll Environm &

    Energy Engn Beijing Key Lab Green Catalysis &

    Separat Beijing 100124 Peoples R China;

    Beijing Univ Technol Coll Environm &

    Energy Engn Beijing Key Lab Green Catalysis &

    Separat Beijing 100124 Peoples R China;

    Taiyuan Univ Technol Res Inst Special Chem Taiyuan 030024 Shanxi Peoples R China;

    Beijing Univ Technol Coll Environm &

    Energy Engn Beijing Key Lab Green Catalysis &

    Separat Beijing 100124 Peoples R China;

    Beijing Univ Technol Coll Environm &

    Energy Engn Beijing Key Lab Green Catalysis &

    Separat Beijing 100124 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学工业;
  • 关键词

    copper(II) paddlewheel; octatopic ligand; hydrolytic stability; water-vapor adsorption; aniline capture and detection;

    机译:铜(II)桨轮;迁移剂;水解稳定性;水蒸气吸附;苯胺捕获和检测;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号