Stable Metal-Organic Framework-Supported Niobium Catalysts

被引:85
作者
Ahn, Sol [1 ]
Thornburg, Nicholas E. [1 ]
Li, Zhanyong [2 ]
Wang, Timothy C. [2 ]
Gallington, Leighanne C. [3 ]
Chapman, Karena W. [3 ]
Notestein, Justin M. [1 ]
Hupp, Joseph T. [2 ]
Farha, Omar K. [2 ,4 ]
机构
[1] Northwestern Univ, Dept Chem & Biol Engn, 2145 Sheridan Rd, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA
[3] Argonne Natl Lab, Adv Photon Source, Xray Sci Div, 9700 South Cass Ave, Argonne, IL 60439 USA
[4] King Abdulaziz Univ, Dept Chem, Fac Sci, Jeddah 21589, Saudi Arabia
基金
美国国家科学基金会;
关键词
ATOMIC LAYER DEPOSITION; HYDROGEN-PEROXIDE; SELECTIVE EPOXIDATION; ALKENE EPOXIDATION; SILICA CATALYSTS; SURFACE; SITE; CYCLOHEXENE; ZR; FUNCTIONALIZATION;
D O I
10.1021/acs.inorgchem.6b02103
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Developing structurally well-defined, supported oxide catalysts remains a significant challenge. Here, we report the grafting of Nb(V) oxide sites onto the nodes of the Zr-based metal organic framework (MOP) NU-1000 as a stable, well-defined catalyst support. Nb(V) oxide was deposited with loadings up to 1.6 mmol/g via two postsynthetic methods: atomic layer deposition in a MOF, and solution-phase grafting in a MOF. Difference envelope density measurements indicated that the two synthetic methods resulted in different local structures of the Nb(V) ions within NU-1000. Despite their high Nb(V) loadings, which were equivalent to >60% surface coverage, nearly all Nb(V) sites of the MOF-supported catalysts were active sites for alkene epoxidation, as confirmed by phenylphosphonic acid titration. The MOF-supported catalysts were more selective than the control Nb-ZrO2 catalyst for cydohexene epoxidation with aqueous H2O2 and were far more active on a gravimetric basis.
引用
收藏
页码:11954 / 11961
页数:8
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