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High Gas Sorption and Metal‐Ion Exchange of Microporous Metal–Organic Frameworks with Incorporated Imide Groups
Author(s) -
Prasad Thazhe Kootteri,
Hong Dae Ho,
Suh Myunghyun Paik
Publication year - 2010
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201002135
Subject(s) - sorption , imide , metal organic framework , adsorption , microporous material , ion exchange , metal , ligand (biochemistry) , chemistry , inorganic chemistry , nuclear chemistry , materials science , ion , polymer chemistry , organic chemistry , biochemistry , receptor
Metal–organic frameworks (MOFs), {[Cu 2 (bdcppi)(dmf) 2 ] ⋅ 10DMF ⋅ 2H 2 O} n (SNU‐50) and {[Zn 2 (bdcppi)(dmf) 3 ] ⋅ 6DMF ⋅ 4H 2 O} n (SNU‐51), have been prepared by the solvothermal reactions of N , N '‐bis(3,5‐dicarboxyphenyl)pyromellitic diimide (H 4 BDCPPI) with Cu(NO 3 ) 2 and Zn(NO 3 ) 2 , respectively. Framework SNU‐50 has an NbO‐type net structure, whereas SNU‐51 has a PtS‐type net structure. Desolvated solid [Cu 2 (bdcppi)] n (SNU‐50'), which was prepared by guest exchange of SNU‐50 with acetone followed by evacuation at 170 °C, adsorbs high amounts of N 2 , H 2 , O 2 , CO 2 , and CH 4 gases due to the presence of a vacant coordination site at every metal ion, and to the presence of imide groups in the ligand. The Langmuir surface area is 2450 m 2 g −1 . It adsorbs H 2 gas up to 2.10 wt % at 1 atm and 77 K, with zero coverage isosteric heat of 7.1 kJ mol −1 , up to a total of 7.85 wt % at 77 K and 60 bar. Its CO 2 and CH 4 adsorption capacities at 298 K are 77 wt % at 55 bar and 17 wt % at 60 bar, respectively. Of particular note is the O 2 adsorption capacity of SNU‐50' (118 wt % at 77 K and 0.2 atm), which is the highest reported so far for any MOF. By metal‐ion exchange of SNU‐51 with Cu II , {[Cu 2 (bdcppi)(dmf) 3 ] ⋅ 7DMF ⋅ 5H 2 O} n (SNU‐51‐Cu DMF ) with a PtS‐type net was prepared, which could not be synthesized by a direct solvothermal reaction.