Complexation of trivalent lanthanide cations by D-ribose in the solid state. The crystal structure and FT-IR study of PrCl3 center dot alpha-D-ribopyranose center dot 5 H2O
Lm. Yang et al., Complexation of trivalent lanthanide cations by D-ribose in the solid state. The crystal structure and FT-IR study of PrCl3 center dot alpha-D-ribopyranose center dot 5 H2O, CARBOHY RES, 334(2), 2001, pp. 91-95
The crystal structure of praseodymium chloride-alpha -D-ribopyranose pentah
ydrate, PrCl3.C5H(1)O5.5 H2O, M-r = 487.47, a = 9.1989(8), b = 8.8214(7), c
= 9.8233(9) Angstrom, beta = 94.060(3)degrees, V= 795.2(1) Angstrom (3), Z
= 2, mu = 0.71073 Angstrom and R = 0.0418 for 1923 observed reflections an
d 172 parameters has been determined. The sugar provides three hydroxyl gro
ups, ax-eq-ax for coordination. The Pr3+ ion is nine-coordinated with five
Pr-O bonds from water molecules, three from hydroxyl groups and one from ch
loride. The OH, CO stretching vibrations and COH bending vibrations are shi
fted in the complex IR spectrum and the hydroxyl groups, water molecules, c
hloride ions form an extensive hydrogen-bond network. (C) 2001 Published by
Elsevier Science Ltd.