Synthesis, properties, and structure of the complexes of divalent metals with 1-hydroxyethane-1,1-diphosphonic acid (H4L), [(HOCH2CH2)(3)NH][M-II(H2.5L)(2)(H2O)(2)]center dot 5H(2)O. Crystal structure of triethanolammonium Bis(1-hydroxyethane-1,1-diphosphonato)diaquacuprate(II) pentahydrate
Vs. Sergienko et al., Synthesis, properties, and structure of the complexes of divalent metals with 1-hydroxyethane-1,1-diphosphonic acid (H4L), [(HOCH2CH2)(3)NH][M-II(H2.5L)(2)(H2O)(2)]center dot 5H(2)O. Crystal structure of triethanolammonium Bis(1-hydroxyethane-1,1-diphosphonato)diaquacuprate(II) pentahydrate, RUSS J C CH, 25(2), 1999, pp. 123-131
The synthesis of a series of the [(HOCH2CH2)(3)NH] [M-II(H2.5L)(2)(H2O)(2)]
. 5H(2)O (M-II = Cu, Zn, Mg, Mn, Co, and Ni) compounds is reported. All cr
ystals are isostructural. X-ray structural analysis is carried out for the
copper(II) complex. The complexed anion has the cis structure. The coordina
tion polyhedron of the metal atom is a prolate tetragonal bipyramid (4 + 2)
, with one of the four O(L) atoms and one of the two O(w) atoms of the H2O
molecules occupying axial positions. The bond lengths are Cu-O(eq) 1.982-1.
996 Angstrom (L) and 1.986 Angstrom (H2O) and Cu-O(ax) 2.428 Angstrom (L) a
nd 2.311 Angstrom (H2O). The anionic complexes, the triethanolammonium cati
ons, and H2O molecules of crystallization are joined together by the branch
ed network of hydrogen bonds. The influence of cation nature and compositio
n of hydrate shell on the "choice" of geometrical isomer (trans or cis) is
discussed for the 3d complexes [M-II(H4-nL)(2)(H2O)(2)](-2n+2).