4.8 Article

Cooperativity and Metal-Linker Dynamics in Spin Crossover Framework Fe(1,2,3-triazolate)2

Journal

CHEMISTRY OF MATERIALS
Volume 33, Issue 21, Pages 8534-8545

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.1c03143

Keywords

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Funding

  1. University of Oregon
  2. National Science Foundation through the Division of Materials Research [DMR-1956403]
  3. Department of Energy through the Office of Basic Energy Sciences [DE-SC0022147]
  4. University of Oregon through the Office of Vice President for Research and Innovation
  5. U.S. Department of Energy (DOE) [DE-SC0022147] Funding Source: U.S. Department of Energy (DOE)

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This study combines experimental and computational approaches to identify the origin of cooperative interactions in metal-organic frameworks, demonstrating the importance of dynamic metal-linker bonding in triggering cooperative SCO transitions. The research highlights the significant role of dynamic bonding in the functional behavior of framework materials and provides a roadmap for understanding the manipulation of SCO behavior in general.
Cooperative interactions are responsible for the useful properties of spin crossover (SCO) materials-large hysteresis windows, critical temperatures near room temperature, and abrupt transitions-with hybrid framework materials exhibiting the greatest cooperativity and hysteresis of all SCO systems. However, little is known about the chemical origin of cooperativity in frameworks. Here, we present a combined experimental-computational approach for identifying the origin of cooperativity in the metal-organic framework (MOF) Fe(1,2,3-triazolate)(2) (Fe(TA)(2)), which exhibits the largest known hysteresis window of all SCO materials and unusually high transition temperatures, as a roadmap for understanding the manipulation of SCO behavior in general. Variable-temperature vibrational spectroscopy provides evidence that soft modes associated with dynamic metal-linker bonding trigger the cooperative SCO transition. Thermodynamic analysis also confirms a cooperativity magnitude much larger than those of other SCO systems, while electron density calculations of Fe(TA)(2) support previous theoretical predictions that large cooperativity arises in materials where SCO produces considerable differences in metal-ligand bond polarities between different spin states. Taken together, this combined experimental-computational study provides a microscopic basis for understanding cooperative magnetism and highlights the important role of dynamic bonding in the functional behavior of framework materials.

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