4.8 Article

Active-Site-Accessible, Porphyrinic Metal-Organic Framework Materials

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 133, Issue 15, Pages 5652-5655

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja111042f

Keywords

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Funding

  1. NU-ICEP, NU-NSEC, DTRA [HDTRA-09-1-0007]
  2. AFOSR
  3. U.S. DOE, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  4. NSF/DOE [NSF/CHE-0822838]
  5. Michigan Economic Development Corporation
  6. Michigan Technology Tri-Corridor [085P1000817]
  7. Direct For Mathematical & Physical Scien
  8. Division Of Chemistry [0822838] Funding Source: National Science Foundation

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On account of their structural similarity to cofactors found in many metallo-enzymes, metalloporphyrins are obvious potential building blocks for catalytically active, metal-organic framework (MOF) materials. While numerous porphyrin-based MOFs have already been described, versions featuring highly accessible active sites and permanent micro-porosity are remarkably scarce. Indeed, of the more than 70 previously reported porphyrinic MOFs, only one has been shown to be both permanently microporous and contain internally accessible active sites for chemical catalysis. Attempts to generalize the design approach used in this single successful case have failed. Reported here, however, is the synthesis of an extended family of MOFs that directly incorporate a variety of metalloporphyrins (specifically Al3+, Zn2+, Pd2+, Mn3+, and Fe3+ complexes). These robust porphyrinic materials (RPMs) feature large channels and readily accessible active sites. As an illustrative example, one of the manganese-containing RPMs is shown to be catalytically competent for the oxidation of alkenes and alkanes.

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