4.8 Article

Enhancing Pore-Environment Complexity Using a Trapezoidal Linker: Toward Stepwise Assembly of Multivariate Quinary Metal-Organic Frameworks

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 140, Issue 39, Pages 12328-12332

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b07411

Keywords

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Funding

  1. Center for Gas Separations Relevant to Clean Energy Technologies, an Energy Frontier Research Center - U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0001015]
  2. Robert A. Welch Foundation through a Welch Endowed Chair [A-0030]
  3. National Science Foundation Graduate Research Fellowship [DGE: 1252521]
  4. U.S. Department of Energy Office of Fossil Energy National Energy Technology Laboratory [DEFE0026472]
  5. National Science Foundation Small Business Innovation Research (NSF-SBIR) program [1632486]
  6. Dow Chemical Graduate Fellowship

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Multicomponent metal-organic frameworks (MOFs) promise the precise placement of synergistic functional groups with atomic-level precision, capable of promoting fascinating developments in basic sciences and applications. However, the complexity of multicomponent systems poses a challenge to their structural design and synthesis. Herein, we show that linkers of low symmetry can bring new opportunities to the construction of multicomponent MOFs. A carbazole-tetracarboxylate linker of C-s point group symmetry was designed and combined with an 8-connected Zr-6 cluster to generate a low-symmetry MOF, PCN-609. PCN-609 contains coordinatively unsaturated Zr sites arranged within a lattice with three crystallographically distinct pockets, which can accommodate linear linkers of different lengths. Sequential linker installation was carried out to postsynthetically insert three linear linkers into PCN-609, giving rise to a quinary MOF. Functionalization of each linker from the quinary MOF system creates multivariate pore environments with unprecedented complexity.

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