4.8 Article

Reticular Access to Highly Porous acs-MOFs with Rigid Trigonal Prismatic Linkers for Water Sorption

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 141, 期 7, 页码 2900-2905

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b13710

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资金

  1. Defense Threat Reduction Agency [HDTRA1-18-1-0003]
  2. Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource [NSF NNCI-1542205]
  3. MRSEC program at the Materials Research Center [NSF DMR-1720139]
  4. International Institute for Nanotechnology (IIN)
  5. Keck Foundation
  6. State of Illinois, through the IIN
  7. NSF [CHE-1048773, DMR0521267]
  8. SHyNE Resource [NSF NNCI-1542205]
  9. State of Illinois
  10. IIN

向作者/读者索取更多资源

Metal-organic frameworks (MOFs) based on edge-transitive 6-c acs nets are well-developed and can be synthesized from trinuclear metal clusters and ditopic ligands, i.e., MOF-235 and MIL-88. The rational design of noncatenated acs-MOFs by symmetry-matching between trigonal prismatic organic ligands and trinuclear clusters, however, remains a great challenge. Herein, we report a series of acs-MOFs (NU-1500) based on trivalent trinuclear metal (Fe3+, Cr3+, and Sc3+) clusters and a rigid trigonal prismatic ligand courtesy of reticular chemistry. The highly porous and hydrolytically stable NU-1500-Cr can be activated directly from water and displays an impressive water vapor uptake with small hysteresis.

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