期刊
INORGANIC CHEMISTRY
卷 57, 期 20, 页码 12961-12968出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.8b02212
关键词
-
资金
- NSFC [21573042, 21673039]
- Fujian Science and Technology Department [2016J01046, 2014J06003, 2014H6007]
- Recruitment Program of Global Young Experts
Poor stability has been one of the major difficulties affecting to the practical application of metal organic frameworks (MOFs). In this work, we obtained two 3D structurally isomeric Cd-MOFs, {[Cd-6(NH2Me2)(2)(PTB)(4)(HCOO)(2)(H2O)]center dot(DMF)13 center dot(H2O)(4)}(n) (FJU-35) and {[Cd-6(NH2Me2)(2)-(PTB)(4 center dot)(HCOO)(2)](DMF)(6)center dot(H2O)(2)}(n) (FJU-36) (H3PTB = pyridine-2,4, 6-tribenzoic acid) containing different Cd-II-O-Cd-II chains by varying the addition agents. FJU-35 with coordinated solvent and formate in asymmetric mu(3)-eta(1):eta(2) coordination mode within the CdII-O-Cd-II chains is vulnerable to external attacks and is apt to collapse after activation, while FJU-36 with no coordinated solvent in the Cd-II-O-Cd-II chains but fully protected by the carboxylates from the ligands and the symmetric formate in the coordination mode mu(3)-eta(2):eta(2) is stable, and its activated sample shows efficient separation of C2H2/CH4 and C2H2/CO2 mixtures. Conversely, FJU-35 with more vulnerability is more sensitive to the detection of nitrobenzene than FJU-36.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据