The copper(II) complexes formed by the imidazolinone herbicide Imazapy
r or propyl-4-methyl-5-oxo-2-imidazolin-2-yl)-nicotinic acid (H(2)imz)
are described. The compounds isolated in the solid state confirm that
Imazapyr is a versatile bipy-like ligand able to chelate the metal io
n through two different donor sets. The pair of pyridine and imidazole
nitrogen atoms is bound to copper in [Cu(Himz)(2)] and [Cu(Himz)(2)(H
2O)]. In these, a five-coordination at the metal ion and a geometry cl
ose to the trigonal bipyramid are favoured. The weak carboxylate group
does not play a primary role in the complex formation properties of I
mazapyr. However, its involvement yields the polymetallic compounds [C
u(Himz)(2)] and [Cu-3(Himz)(4)(H2O)(4)](NO3)(2). The deprotonation of
the lactam group provides Imazapyr with a stronger donor set, the lact
am and the pyridine nitrogens, yielding 1:1 polymeric complexes [Cu(im
z)(H2O)] and [Cu(imz)(H2O)(3)]. H2O. With the methyl ester of Imazapyr
(HimzOMe), the different charge of the ligand deprotonated at the lac
tam group allows a bis-chelated complex [Cu(imzOMe)(2)(H2O)]. H2O in w
hich the metal ion adopts a five-coordination. Analogies have been est
ablished between the complexes of H(2)imz, HimzOMe and 2,2'-bipyridine
.