Crystals of bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)bis-pyrimidinecop
per(II) (1), bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)bis(4-methylpyri
midine)copper(II) (2), bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)bis(qu
inazoline)- copper(II) (3) showed ferromagnetic interactions at extremely l
ow temperature. Crystal structure analyses revealed that these complexes we
re catena-bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)[mu -pyrimidine-N-1
:N-3]copper(II), [Cu(hfac)(2)-(pm)(2)](n), catena-bis(1,1,1,5,5,5-hexafluo
ropentane-2,4-dionato)[mu -4-methylpyrimidine-N-1:N-3]copper(II), [Cu(hfac)
(2)(4-Me-pm)](n), and catena-bis(1,1,1,5,5,5-hexafluoropentane-2,4-dionato)
[mu -pyrimidine-N-1 :N-3]copper(II), [Cu(hfac)(2)-(qz)](n), for (1), (2) an
d (3), respectively. In (1) and (2) the pyrimidines bridge the Cu atoms wit
h 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-methylpyri
midine complex (4), showing paramagnetic properties, was revealed to be a t
rinuclei complex bridged by two 4-methylpyrimidines, tris[bis(1,1,1,5,5,5-h
exafluoropentane-2,4-dionato)copper(II)][bis-mu -4-methyl-pyrimidine-N-1:N-
3]. The chain structures with an axial-equatorial coordination mode of the
bridging organic moieties should play an important role in the appearance o
f the ferromagnetic interactions.