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Lonothermal synthesis and magnetic studies of novel two-dimensional metal - Formate frameworks

  • Paul J. Calderone
  • , Paul M. Forster
  • , Lauren A. Borkowski
  • , Simon J. Teat
  • , Mikhail Feygenson
  • , Meigan C. Aronson
  • , John B. Parise
  • Stony Brook University
  • University of Nevada, Las Vegas
  • Lawrence Berkeley National Laboratory
  • Brookhaven National Laboratory Condensed Matter Physics and Materials Science Department

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Five novel two-dimensional frameworks containing formatebridged metal-centered octahedra are synthesized ionothermally from two ionic liquids previously unused as solvents in hybrid synthesis, 2-hydroxyethylammonium (HEA) formate, and 1-hydroxy-3-proplyammonium (HPA formate. Templating effects of the cation from each ionic liquid drive the formation of different structures. [NH3C2H4OH]2[M(CHO2) 4](l:M = Co, 2: M = Ni) exhibit the same stoichiometry and connectivity as their manganese analogue (3: M = Mn), but the manganese form exhibits a different topology from 1 and 2.[NH3C3H 6OH][M(CHO2)3(H2O)] (4:M = Co, 5:M = Mn) were synthesized using the HPA formate ionic liquid with a metal-formate connectivity related to those of 1-3. Canted antiferromagnetic ordering occurs at low temperatures (1: TN = 7.0 K, 2: TN = 4.6 K, 3: TN = 8.0 K, 4: TN = 7.0 K, 5: TN = 9.2 K), similar to the magnetic properties previously reported for other metal-formate hybrid materials.

Original languageEnglish
Pages (from-to)2159-2167
Number of pages9
JournalInorganic Chemistry
Volume50
Issue number6
DOIs
StatePublished - Mar 21 2011

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