Functional Mesoporous Metal-Organic Frameworks for the Capture of Heavy Metal Ions and Size-Selective Catalysis

被引:273
作者
Fang, Qian-Rong [1 ]
Yuan, Da-Qian [1 ]
Sculley, Julian [1 ]
Li, Jian-Rong [1 ]
Han, Zheng-Bo [1 ]
Zhou, Hong-Cai [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA
基金
美国国家科学基金会;
关键词
POROUS COORDINATION POLYMER; PERMANENT POROSITY; CRYSTAL-STRUCTURE; HYDROGEN STORAGE; SURFACE-AREA; DESIGN; CHEMISTRY; TOPOLOGY; SEPARATION; COMPLEXES;
D O I
10.1021/ic101935f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
By using Zn4O(CO2)(6) as secondary building units (SBUs) and two extended ligands containing amino functional groups, TATAB and BTATB (TATAB = 4,4',4 ''-s-triazine-1,3,5-triyltri-p-aminobenzoate and BTATB = 4,4',4 ''-(benzene-1,3,5-triyltris(azanediyl))tribenzoate), two isostructural mesoporous metal organic frameworks (MOFs) with cavities up to 2.73 nm, designated as PCN-100 and PCN-101 (PCN represents porous coordination network), have been synthesized. N-2 sorption isotherms of both PCN-100 and -101 showed typical type IV behavior, indicating their mesoporous nature. The TATAB ligand that comprises PCN-100 was employed to capture heavy metal ions (Cd(II) and Hg(II)) by constructing complexes within the pores with a possible coordination mode similar to that found in aminopyridinato complexes. This reveals that mesoporous materials such as PCN-100 can be applied in the elimination of heavy metal ions from waste liquid. In addition, both PCNs-100 and -101 exhibit size-selective catalytic activity toward the Knoevenagel condensation reaction.
引用
收藏
页码:11637 / 11642
页数:6
相关论文
共 41 条
[1]  
Blake AJ, 2010, NAT CHEM, V2, P688, DOI [10.1038/nchem.681, 10.1038/NCHEM.681]
[2]   A route to high surface area, porosity and inclusion of large molecules in crystals [J].
Chae, HK ;
Siberio-Pérez, DY ;
Kim, J ;
Go, Y ;
Eddaoudi, M ;
Matzger, AJ ;
O'Keeffe, M ;
Yaghi, OM .
NATURE, 2004, 427 (6974) :523-527
[3]   Design of frameworks with mixed triangular and octahedral building blocks exemplified by the structure of [Zn4O(TCA)2] having the pyrite topology [J].
Chae, HK ;
Kim, J ;
Friedrichs, OD ;
O'Keefe, M ;
Yaghi, OM .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (33) :3907-3909
[4]   SYNTHESES, MOLECULAR-STRUCTURES AND ELECTROCHEMICAL-BEHAVIOR OF 2 ISOMERIC RU(PHNPY)2(PPH3)2 COMPLEXES [J].
CHAKRAVARTY, AR ;
COTTON, FA ;
SHAMSHOUM, ES .
INORGANICA CHIMICA ACTA-ARTICLES AND LETTERS, 1984, 86 (01) :5-11
[5]   Interwoven metal-organic framework on a periodic minimal surface with extra-large pores [J].
Chen, BL ;
Eddaoudi, M ;
Hyde, ST ;
O'Keeffe, M ;
Yaghi, OM .
SCIENCE, 2001, 291 (5506) :1021-1023
[6]   A chemically functionalizable nanoporous material [Cu3(TMA)2(H2O)3]n [J].
Chui, SSY ;
Lo, SMF ;
Charmant, JPH ;
Orpen, AG ;
Williams, ID .
SCIENCE, 1999, 283 (5405) :1148-1150
[7]   Synthesis and structure of the first non 'ate' heteroleptic lanthanoid complexes bearing monoanionic 2-amidopyridine ligands [J].
Cole, ML ;
Junk, PC .
NEW JOURNAL OF CHEMISTRY, 2003, 27 (07) :1032-1037
[8]   New chemistry of the triply bonded divanadium (V24+) unit and reduction to an unprecedented V23+ core [J].
Cotton, FA ;
Hillard, EA ;
Murillo, CA ;
Wang, XP .
INORGANIC CHEMISTRY, 2003, 42 (19) :6063-6070
[9]   Hydrogen storage in microporous metal-organic frameworks with exposed metal sites [J].
Dinca, Mircea ;
Long, Jeffrey R. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (36) :6766-6779
[10]   Systematic design of pore size and functionality in isoreticular MOFs and their application in methane storage [J].
Eddaoudi, M ;
Kim, J ;
Rosi, N ;
Vodak, D ;
Wachter, J ;
O'Keeffe, M ;
Yaghi, OM .
SCIENCE, 2002, 295 (5554) :469-472