4.7 Article

Stable Metal-Organic Framework-Supported Niobium Catalysts

Journal

INORGANIC CHEMISTRY
Volume 55, Issue 22, Pages 11954-11961

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.6b02103

Keywords

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Funding

  1. Inorganometallic Catalyst Design Center, an EFRC - U.S. Department of Energy (DOE), Office of Basic Energy Sciences [DE-SC0012702]
  2. Dow Chemical Company
  3. MRSEC program of the National Science Foundation at the Materials Research Center of Northwestern Univ. [DMR-1121262]
  4. MRSEC program (NSF) at the Materials Research Center [DMR-1121262]
  5. International Institute for Nanotechnology (IIN)
  6. State of Illinois through the IIN
  7. DOE Office of Science by Argonne National Laboratory [DE-AC02-06CH11357]

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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.

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