Ring-Opening Reactions within Porous Metal-Organic Frameworks

被引:117
作者
Britt, David [1 ]
Lee, Chain [1 ]
Uribe-Romo, Fernando J. [1 ]
Furukawa, Hiroyasu [1 ]
Yaghi, Omar M. [1 ]
机构
[1] Univ Calif Los Angeles, Ctr Reticular Chem, Calif NanoSyst Inst, Dept Chem & Biochem, Los Angeles, CA 90095 USA
关键词
DESIGN; FUNCTIONALIZATION; SEPARATION; MOFS; CO2;
D O I
10.1021/ic100652x
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two new metal organic framework (MOF) structures, IRMOF-3b and -3c, were prepared by ring-opening reaction of 1,3-propane-sultone and 2-methylaziridine with an amine functionalized MOF, IRMOF-3. The new structures are permanently functionalized with covalently linked sulfonate and alkyamine units, respectively. The underlying framework structure is retained after reaction as confirmed by powder X-ray diffraction. The high porosity of IRMOF-3 is also maintained, as evidenced by nitrogen adsorption experiments, which yield Brunauer-Emmett-Teller (BET) surface areas of 1380 and 530 m(2) g(-1) compared to 2040 m(2) g(-1) in the parent material. Ring-opening reactions provide a versatile route to irreversible binding of a range of functionalities that are otherwise difficult to access in MOFs.
引用
收藏
页码:6387 / 6389
页数:3
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