An in situ self-assembly template strategy for the preparation of hierarchical-pore metal-organic frameworks

نویسندگان

  • Hongliang Huang
  • Jian-Rong Li
  • Keke Wang
  • Tongtong Han
  • Minman Tong
  • Liangsha Li
  • Yabo Xie
  • Qingyuan Yang
  • Dahuan Liu
  • Chongli Zhong
چکیده

Metal-organic frameworks (MOFs) have recently emerged as a new type of nanoporous materials with tailorable structures and functions. Usually, MOFs have uniform pores smaller than 2 nm in size, limiting their practical applications in some cases. Although a few approaches have been adopted to prepare MOFs with larger pores, it is still challenging to synthesize hierarchical-pore MOFs (H-MOFs) with high structural controllability and good stability. Here we demonstrate a facile and versatile method, an in situ self-assembly template strategy for fabricating stable H-MOFs, in which multi-scale soluble and/or acid-sensitive metal-organic assembly (MOA) fragments form during the reactions between metal ions and organic ligands (to construct MOFs), and act as removable dynamic chemical templates. This general strategy was successfully used to prepare various H-MOFs that show rich porous properties and potential applications, such as in large molecule adsorption. Notably, the mesopore sizes of the H-MOFs can be tuned by varying the amount of templates.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Highly mesoporous metal–organic framework assembled in a switchable solvent

The mesoporous metal-organic frameworks are a family of materials that have pore sizes ranging from 2 to 50 nm, which have shown promising applications in catalysis, adsorption, chemical sensing and so on. The preparation of mesoporous metal-organic frameworks usually needs the supramolecular or cooperative template strategy. Here we report the template-free assembly of mesoporous metal-organic...

متن کامل

Metal-organic frameworks of cobalt and nickel centers with carboxylate and pyridine functionality linkers: Thermal and physical properties; precursors for metal oxide nanoparticle preparation

This  article  provides  an  overview  on  preparation,  design,  crystal structure  and  properties  of  some  metal-organic  frameworks  of carboxylate coordination polymers mixed with pyridine-functionality linkers  prepared  in  our  laboratory.  The  article  covers  coordination polymers  in  two-  and  three-dimensional  supramolecular architectures. The reported coordination polyme...

متن کامل

Effects of ultrasound on properties of ni-metal organic framework nanostructures

Objective(s): According to the unique properties of magnetic nanoparticles, Nickel Metal-Organic Frameworks (MOF) was synthesized successfully by ultrasound irradiation. Metal-organic frameworks (MOFs) are organic–inorganic hybrid extended networks that are constructed via covalent linkages between metal ions/metal clusters and organic ligands called a linker. Materials and Methods: The nanopar...

متن کامل

Effect of the pillar ligand on preventing agglomeration of ZnO nanoparticles prepared from Zn(II) metal-organic frameworks

Metal-Organic Frameworks (MOFs) represent a new class of highly porous materials. On this regard,  two nano porous metal-organic frameworks of [Zn2(1,4-bdc)2(H2O)2∙(DMF)2]n (1) and [Zn2(1,4-bdc)2(dabco)]·4DMF·1⁄2H2O (2), (1,4-bdc = benzene-1,4-dicarboxylate, dabco = 1,4-diaza...

متن کامل

Facile and Efficient Self-template Synthesis of Core-coronal-shell ZnO@ZIF-8 Nanohybrid Using Ascorbic Acid and its Application for Arsenic Removal

In the present contribution, a facile and efficient protocol for synthesis a nanohybrid structure of core-coronal-shell ZnO@ZIF-8 using ascorbic acid (ZnO@AA/ZIF-8) as a new adsorbent for arsenic removal from water has been represented. For this purpose, the ZnO nanospheres were synthesized by a green and simple method followed by coating with ascorbic acid (AA) to modify their surface to achie...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2015