Ho. Stumpf et al., CHEMISTRY AND PHYSICS OF A MOLECULAR-BASED MAGNET CONTAINING 3 SPIN CARRIERS, WITH A FULLY INTERLOCKED STRUCTURE, Journal of the American Chemical Society, 116(9), 1994, pp. 3866-3874
The compound of formula (rad)(2)Mn-2[Cu(opba)](3)(DMSO)(2).2H(2)O (her
eafter abbreviated as (rad)(2)Mn2Cu3) has been synthesized; rad(+) sta
nds for the radical cation dinium-4-yl)-4,4,5,5-tetramethylimidazoline
-1-oxyl 3-oxide, and opba stands for o-phenylenebis(oxamato). The crys
tal structure has been solved (space group, Cc; lattice parameters, a
= 25.379(3) Angstrom, b = 25.146(3) Angstrom, c = 18.845(6) Angstrom,
beta = 131.52(4)degrees, Z = 4) and has revealed quite an unusual arch
itecture. The structure consists of two nearly perpendicular graphite-
like networks with edge-sharing hexagons. The corners of each hexagon
are occupied by Mn(II) ions, and the middles of the edges by Cu(II) io
ns. The two networks are interlocked, the center of each hexagon being
occupied by a Cu(II) ion belonging to a perpendicular hexagon. (rad)(
2)Mn2Cu3 contains three kinds of spin carriers: Mn(II) and Cu(II) ions
, antiferromagnetically coupled through oxamato bridges, and rad(+) ra
dical cations, bridging the Cu(II) ions through the nitronyl nitroxide
groups and forming rad(+)-Cu(II) chains. The magnetic and EPR propert
ies of (rad)(2)Mn2CU3 have been studied in some detail. The temperatur
e dependence of chi(M) T (chi(M) being the molar magnetic susceptibili
ty and T the temperature) shows a minimum around 115 K characteristic
of a ferrimagnetic behavior and then a divergence as T approaches the
very low temperatures. The temperature dependence of the magnetization
has confirmed that a long-range magnetic ordering occurs at T-c = 22.
5 K. The field dependence of the magnetization, M = f(H), has been mea
sured at 4.2 K up to 200 kOe. The compound behaves as a soft magnet, w
ith a very weak coercive field. The M = f(H) curve shows an extremely
high zero-field susceptibility, as expected for a magnet and then a sm
ooth increase of M as H increases. This behavior has been attributed t
o the progressive alignment of the rad(+) spins along the field direct
ion. In zero field, the radical cations are antiferromagnetically coup
led with the Mn2Cu3 metal core, a situation which probably results fro
m ferromagnetic interactions between nearest neighbor spin carriers al
ong the rad(+)-Cu(II) chains. The average value of the rad(+)-Cu(II) i
nteraction parameter has been estimated from the high-field range of t
he M = f(H) curve and found as J(radCu) = 11.5 cm(-1) (H=-J(radCu)S(ra
d).S-Cu) The X-band powder EPR spectra have also been investigated. Ab
ove T-c the spectra show a single resonance centered at g = 1.995 at 2
90 K and at g = 1.955 at 23 K. At T-c new features appear, which are s
trongly temperature dependent. A qualitative picture of the ferromagne
tic resonance in (rad)(2)Mn2Cu3 has been proposed. All the structural
and physical data have been discussed, and some perspectives of our fi
ndings have been presented.