The crystal structures of four
[dicyanoargentato(I)]cadmium(II) complexes with the
mixed ligation of imidazole
(imH: C3H4N2) or
N-methyl- or 2-methylimidazole (N-Meim or
2-MeimH: C3H6N2) on the
cadmium(II), [Cd(imH)4{Ag(CN)2}2]
(1a),
[Cd(imH)5{Ag(CN)2}][Ag(CN)2]
(1b),
[Cd(N-Meim)4{Ag(CN)2}][Ag(CN)2]
(2), and
[Cd(2-MeimH)4{Ag(CN)2}][Ag(CN)2]·H2O
(3), have been determined by single-crystal X-ray
diffraction methods.
Complex 1a crystallizes in the orthorhombic
Pbmn space group with a = 22.206(2) Å,
b = 10.306(1) Å, c =
10.318(1) Å, Z = 4. 1b: monoclinic
P21/n, a = 9.028(4)
Å, b = 13.988(6) Å, c = 22.079(4)
Å, β = 101.02(2)°,
Z = 4. 2: monoclinic
C2/m, a = 11.1292(8) Å,
b = 11.435(3) Å, c = 11.266(1) Å,
β = 94.252(8)°, Z = 2.
3:
orthorhombic Pnnm, a = 11.212(2) Å,
b = 11.156(5) Å, c = 23.646(5) Å,
Z = 4. Complex 1a has the shape
of
a four-blade propeller consisting of
[Cd(imH)4]2+ with the shaft being the
monodentate [−NCAgCN]- anions.
1b comprises the discrete
[Ag(CN)2]- and the umbrella-shaped
[Cd(imH)5NCAgCN]+ in which the
monodentate
[Ag(CN)2]- behaves as the shank;
hydrogen-bond networks among the umbrellas build up a
three-dimensional
lattice. In 2 and 3 the four-blade
propellers of
[Cd(N-Meim)4]2+ and
[Cd(2-MeimH)4]2+ are successively
linked
at every Cd by the ambidentate −NCAgCN− rods to form an infinite
chain, respectively; the discrete
[Ag(CN)2]-
anions and the H2O in 3 are accommodated in the
interchain space. The varieties in coordination behavior
of
[Ag(CN)2]- can be interpreted in terms
of the hydrogen-bond formation between a pyrrole H of the
imidazole
ligand and an unbridged N-end of
[Ag(CN)2]-.