Acta Crystallographica Section B

Structural Science

Volume 57, Part 6 (December 2001)


research papers



Acta Cryst. (2001). B57, 772-779    [ doi:10.1107/S0108768101013568 ]

Bis(hfac)-copper(II) complexes bridged by pyrimidines showing magnetic interactions

M. Yasui, Y. Ishikawa, T. Ishida, T. Nogami and F. Iwasaki

Abstract: Crystals of bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)bispyrimidinecopper(II) (1), bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)bis(4-methylpyrimidine)copper(II) (2), bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)bis(quinazoline)copper(II) (3) showed ferromagnetic interactions at extremely low temperature. Crystal structure analyses revealed that these complexes were catena-bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)[[mu]-pyrimidine-N1:N3]copper(II), [Cu(hfac)2(pm)2]n, catena-bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)[[mu]-4-methylpyrimidine-N1:N3]copper(II), [Cu(hfac)2(4-Me-pm)]n, and catena-bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)[[mu]-pyrimidine-N1:N3]copper(II), [Cu(hfac)2(qz)]n, for (1), (2) and (3), respectively. In (1) and (2) the pyrimidines bridge the Cu atoms with an axial-equatorial mode to form one-dimensional spiral chains. Complex (3) also forms a one-dimensional chain structure. The coordination mode of (3) is axial-axial at room temperature, while axial-equatorial at 120 K. On the other hand, the structure of the other modification of the 4-methylpyrimidine complex (4), showing paramagnetic properties, was revealed to be a trinuclei complex bridged by two 4-methylpyrimidines, tris[bis-(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)copper(II)][bis-[mu]-4-methyl-pyrimidine-N1:N3]. The chain structures with an axial-equatorial coordination mode of the bridging organic moieties should play an important role in the appearance of the ferromagnetic interactions.

Keywords: bridging pyrimidine; magnetic interactions; coordination polymer.

 bibliographic record in  format

  Find reference:   Volume   Page   
  Search:     From   to      Advanced search

Copyright © International Union of Crystallography
IUCr Webmaster