Copper(II) complexes with (2-hydroxybenzyl-2-pyridylmethyl)amine-Hbpa: syntheses, characterization and crystal structures of the ligand and [Cu(II)(Hbpa)(2)](ClO4)(2)center dot 2H(2)O
A. Neves et al., Copper(II) complexes with (2-hydroxybenzyl-2-pyridylmethyl)amine-Hbpa: syntheses, characterization and crystal structures of the ligand and [Cu(II)(Hbpa)(2)](ClO4)(2)center dot 2H(2)O, INORG CHIM, 290(2), 1999, pp. 207-212
Copper(II) complexes were synthesized and characterized by means of element
al analysis, IR and visible spectroscopies, EPR and electrochemistry, as we
ll as X-ray structure crystallography. The group consists of discrete monon
uclear units with the general formula [Cu(II)(Hbpa)(2)](A)(2). nH(2)O, wher
e Hbpa = (2-hydroxybenzyl-2-pyridylmethyl)amine and A = ClO4- n = 2 (1), CH
3COO-, n = 3 (2), NO3-, n = 2 (3) and SO42-, n = 3 (4). The structures of t
he ligand Hbpa and complex 1 have been determined by X-ray crystallography.
Complexes 1-4 have had their UV-Vis spectra measured in both MeCN and DMF.
It was observed that the compounds interact with basic solvents, such that
molecules coordinate to the metal in axial positions in which phenol oxyge
n atoms are coordinated in the protonated forms. The epsilon values were al
l less than 1000 M-1 cm(-1). EPR measurements on powdered samples of 1-3 ga
ve g(parallel to)/A(parallel to) values between 105 and 135 cm(-1), typical
for square planar coordination environments. Complex 4 . 3H(2)O exhibits a
behaviour typical for tetrahedral coordination. The electrochemical behavi
our for complexes 1 and 2 was studied showing irreversible redox waves for
both compounds. (C) 1999 Elsevier Science S.A. All rights reserved.