Xf. He et al., Solid and solution studies of ternary copper(II) complexes formed by heteroaromatic N bases and the anion of N,N-bis(2-hydroxyethyl)glycine (bicine), INORG CHIM, 285(2), 1999, pp. 326-331
The crystal structures of [Cu(Bic)(Bz)]ClO4 and [Cu(Bic)(Iq)]ClO4 (Bic(-) =
N,N-bis(2-hydroxyethyl)glycinate, Bz = benzimidazole and Iq = isoquinoline
) were determined by single-crystal X-ray diffraction techniques. [Cu(Bic)(
Bz)]ClO4: monoclinic system, space group P2(1)/n, a = 7.2212(9), b = 20.824
(4), c = 11.376(2) Angstrom, beta = 93.841(17)degrees, Z = 4. [Cu(Bic)(Iq)]
ClO4: triclinic system. space group P-1, a = 7.490(3), b = 8.268(3), c = 15
.752(6) Angstrom, alpha = 98.620(10), beta = 96.420(10), gamma = 111.470(10
)degrees, Z = 2. In both complexes, the copper atom is five-ligated by an o
xygen atom of the carboxylato group, two hydroxyl oxygen atoms, a nitrogen
atom of bicinate and a nitrogen atom of benzimidazole or isoquinoline. Howe
ver, the stereochemistry is trigonal-bipyramidal and square-pyramidal for C
u(Bic)(Bz)(+) and Cu(Bic)(Iq)(+), respectively. The molecular structures of
these two complexes in aqueous solution are different from those in the cr
ystalline state. ESR and electronic spectra show that the structures of the
se complexes are octahedral in aqueous solution. The stability constants of
these two ternary complexes were determined by pH titration. (C) 1999 Else
vier Science S.A. All rights reserved.