4.8 Article

Direct Imaging of Isolated Single-Molecule Magnets in Metal Organic Frameworks

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 141, Issue 7, Pages 2997-3005

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.8b11374

Keywords

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Funding

  1. Clarkson University
  2. National Institute of Standards and Technology, U.S. Department of Commerce
  3. National Science Foundation [CHE-9974899]
  4. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy [DE-FG02-02ER45999]
  5. King Abdullah University of Science and Technology through center competitive fund [FCC/1/1972-34]
  6. Defense Threat Reduction Agency [HDTRA1-18-1-0003]

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Practical applications involving the magnetic bistability of single-molecule magnets (SMMs) for next-generation computer technologies require nanostructuring, organization, and protection of nanoscale materials in two- or three-dimensional networks, to enable read-and-write processes. Owing to their porous nature and structural long-range order, metal organic frameworks (MOFs) have been proposed as hosts to facilitate these efforts. Although probing the channels of MOF composites using indirect methods is well established, the use of direct methods to elucidate fundamental structural information is still lacking. Herein we report the direct imaging of SMMs encapsulated in a mesoporous MOF matrix using high resolution transmission electron microscopy. These images deliver, for the first time, direct and unambiguous evidence to support the adsorption of molecular guests within the porous host. Bulk magnetic measurements further support the successful nanostructuring of SMMs. The preparation of the first magnetic composite thin films of this kind furthers the development of molecular spintronics.

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