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Structural versatility driven by the flexible di(4-pyridyl) sulfide ligand: from mononuclear cobalt(II) species to sheet-like copper(II) architectures

  • Natalia V. Reis
  • , Maria Vanda Marinho
  • , Tatiana Renata G. Simões
  • , Karina C. Metz
  • , Raphael C. Vaz
  • , Willian X. C. Oliveira
  • , Cynthia L. M. Pereira
  • , Wdeson P. Barros
  • , Carlos B. Pinheiro
  • , Siddhartha O. K. Giese
  • , David L. Hughes
  • , Kleber R. Pirota
  • , Wallace C. Nunes
  • , Humberto O. Stumpf

    Research output: Contribution to journalArticlepeer-review

    6 Citations (Scopus)
    10 Downloads (Pure)

    Abstract

    The reaction between the ligand di(4-pyridyl)sulfide(dps) and two salts of divalent first row transition metals (M= Co2+, and Cu2+) resulted in three new compounds with formula: [Co(dps)4(H2O)2](ClO4)2⋅H2O (1), [Cu(dps)2(dmso)2]n(ClO4)2n (2) and [{Cu(dps)2(dmso)2}{Cu(dps)2(dmso)(H2O)}]n(ClO4)4n2nH2O⋅n(dmso) (3). Crystal structures of 1-3 were determined using single-crystal X-ray diffraction. Crystal structures of 1 consists of mononuclear complexes, in which the dps ligand acts in a monodentate mode through one of the pyridyl nitrogen atoms. Compounds 2 and 3 present the dps ligand bridging metal centers leading to bidimensional coordination polymers. Magnetic properties in the polycrystalline samples of 1-3 in the 300 to 2K temperature range were investigated. Complex 1 exhibits a field-induced slow magnetization behavior and behaves as a single-ion magnet with an effective energy barrier for the reversal of magnetization of 22.9 (1.1) K andτ0= 5.3(1.2)x10−7 s.
    Original languageEnglish
    Pages (from-to)203-211
    JournalPolyhedron
    Volume171
    Early online date17 Jul 2019
    DOIs
    Publication statusPublished - Oct 2019

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