Ps. Mansingh et al., DIOXOURANIUM(VI) AND THORIUM(IV) COMPLEXES OF 1-METHYL-2,2'-BISIMIDAZOLE, Indian journal of chemistry. Sect. A: Inorganic, physical, theoretical & analytical, 34(8), 1995, pp. 639-642
The biheterocyclic nitrogen donor ligand 1-methyl-2,2'-bisimidazole (M
BIM) reacts with UO(2)X(2) and ThX(4) to form mononuclear complexes of
the types UO2 (MBIM)X(2) (X = Cl, I, NCS, NO3, CH3COO, 0.5 SO4) and T
h(MBIM)(2)X(4) (X = NO3, I). The complexes are characterised by elemen
tal analyses, conductivity, thermogravimetry and IR, NMR as well as ma
ss spectra The IR spectra of uranyl complexes exhibit nu(U = 0) in the
regions 900-925 and 825-860 cm(-1) in addition to the vibrational ban
ds of the ligand and those of the polyatomic anions. The H-1 NMR spect
ra of the ligand and the complexes are identical, with the -CH3 group
resonating at 3.5 ppm and the NH proton at 3.9 ppm region. The ring pr
otons are observed as multiplets in the region of 7.0 to 8.0 ppm. The
mass spectra of the ligand gives molecular ion peak at m/z 148 and oth
er fragmentation products, which are appropriately assigned. However,
for the complexes neither the molecular ion peak nor the metallated fr
agmentation patterns are observed. Thermogravimetry shows the loss of
ligands in stages, finally forming the stable metal oxides as the end
product.