DINUCLEAR COPPER(II) AND COBALT(II) COMPLEXES OF THE TETRADENTATE LIGAND 1,2,4,5-TETRAKIS(BENZIMIDAZOL-2-YL)BENZENE (BTBI) - METALLACYCLIC AND NONMETALLACYCLIC DERIVATIVES - X-RAY CRYSTAL-STRUCTURES OF CL-2][CU-2(BTBI)CL-2(DMF)(4)]CL-4-CENTER-DOT-12DMF AND [CO-2(BTBI)BR-4]-4DMF
Ss. Tandon et al., DINUCLEAR COPPER(II) AND COBALT(II) COMPLEXES OF THE TETRADENTATE LIGAND 1,2,4,5-TETRAKIS(BENZIMIDAZOL-2-YL)BENZENE (BTBI) - METALLACYCLIC AND NONMETALLACYCLIC DERIVATIVES - X-RAY CRYSTAL-STRUCTURES OF CL-2][CU-2(BTBI)CL-2(DMF)(4)]CL-4-CENTER-DOT-12DMF AND [CO-2(BTBI)BR-4]-4DMF, Inorganic chemistry, 33(1), 1994, pp. 54-61
BTBI(1,2,4,5-tetrakis(benzimidazol-2-yl) benzene) acts as a tetradenta
te, dinucleating ligand, and on reaction with copper(II) salts forms b
oth 2:1 (metal:ligand) and 2:2 derivatives, depending on reaction cond
itions. Initial reactions between BTBI and a large excess of copper sa
lts produce ''open'' 2:1 derivatives, which rearrange on recrystalliza
tion and disproportionate to form 2:2 ''closed'' metallacyclic complex
es or, with copper halides, species containing both types of cations.
For example, the complex [Cu-2(BTBI)Cl-4(DMF)(2).DMF.H2O (I) produces
[Cu-2(BTBI)(2)Cl-2][Cu-2(BTBI)Cl-2(DMF)Cl-4.12DMF (II) on recrystalliz
ation from DMF/EtOH. With cobalt salts (CoX(2); X = Cl, Br, NCS) ''ope
n'' 2:1 species are formed as the major products: [Co-2(BTBI)X(4)].2DM
F nH(2)O (X = Cl, n = 0.5 (x); x = Br, n = 0 (XI); X = NCS, n = 3 (XII
)). The crystal and molecular structures of compounds II and XI are re
ported. II crystallized in the triclinic system, space group P $$($) o
ver bar 1, with a = 15.538(4) Angstrom, b = 17.044(2) Angstrom, c = 15
.186(4) Angstrom, alpha = 92.11(2)degrees, beta = 98.13(2)degrees, gam
ma = 92.06(2)degrees, V = 3975(2) Angstrom 3, and Z = 2. Refinement by
full-matrix least-squares procedures gave final residuals of R = 0.06
6 and Rw( )= 0.063. Two square-pyramidal copper(II) centers are separa
ted by 8.082(3) Angstrom in the 2:2 centrosymmetric ''closed'' metalla
cyclic cation and by 8.805(3) Angstrom in the 2:1 centrosymmetric ''op
en'' cation, which involves two coordinated DMF molecules per metal ce
nter. XI crystallized in the monoclinic system, space group P2(1)/n, w
ith a = 10.021(2) Angstrom, b = 25.569(4) Angstrom, c = 11.518(2) Angs
trom, beta = 111.78(1)degrees, V = 2700.4(9) Angstrom 3, and Z = 2. Re
finement by full-matrix least-squares techniques gave final residuals
of R = 0.066 and R(w) = 0.072. Compound XI is centrosymmetric with the
two tetrahedral cobalt(II) centers separated by 8.652(3) Angstrom and
the DMF molecules hydrogen-bonded to the NH- benzimidazole moieties.
The spectral and magnetic properties of these complexes are also discu
ssed. Very weak antiferromagnetic exchange exists in most of these com
plexes.