4.7 Article

Open-Framework Iron Fluoride Phosphates Based on Chain, Trinuclear, and Tetranuclear Chain FeIII Building Units: Crystal Structures and Magnetic Properties

Journal

INORGANIC CHEMISTRY
Volume 61, Issue 24, Pages 9257-9268

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.2c00997

Keywords

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Funding

  1. National Natural Science Foundation of China [21671185]
  2. FCT [UID/Multi/04349/2013]
  3. National Research Foundation (NRF) of Korea [2020R1A5A1016518]

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The synthesis and characterization of a series of new open-framework iron fluoride-fluorophosphates with different molecular structures and magnetic properties are reported.
We report the synthesis and characterization of a series of new openframework iron fluoride-fluorophosphates based on linear, trinuclear, and tetranuclear chain Fe-III building units. KFe2(PO3F)(2)F-3 (I) consists of {Fe-2(O3F)(2)F-2}(10-) zigzag chains interconnected by P(O/F)(4) tetrahedra forming a three-dimensional (3D) open framework. K2Fe(PO2.5F1.5)(2)F-2 (II) is built up by {Fe(PO2.5F1.5)(2)F-2}(2-) chains separated by K+ cation layers. The framework for K3Fe3(PO4)(PO3F)(2)F-5 (III) contains two-dimensional {Fe3O4F4(PO3F)(2)}(2-) sheets, which are built from trimeric Fe-octahedra insulated by PO3F tetrahedra. The macroanionic framework of K3Fe4(PO4)(2)F-9 (IV) comprises linear {Fe4O8F9}(10-) chains consisting of tetranuclear magnetic clusters of [Fe4O8F9]10- formed via corner-sharing fluorine atoms decorated with PO4 groups. The magnetic characterization of three iron fluorophosphates reveals diversified magnetism: S = 5/2 spin chains for I, antiferromagnetically coupled triangular Fe units for III, and coupled tetrahedral S = 5/2 spin chains for IV. IV shows strong geometric frustration thanks to its spin motifs of corner-shared tetrahedral clusters.

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