Peroxocopper complexes are of interest in metal ion mediated oxidative
processes and as potential models for the active-site chemistry of co
pper metalloproteins involved in dioxygen (O-2) processing. Having bee
n implicated in certain copper monooxygenases, mononuclear Cu(II)-OOR
species are of particular interest. Here, the generation, spectroscopi
c characterization, and reactivity with triphenylphosphine of three mo
nonuclear acylperoxo-copper(II) complexes are described. [Cu(TMPA)(m-C
lC6H4C(O)OO-)](+) (1; TMPA = tris(2-pyridylmethyl)-amine) was formed b
y low-temperature reaction of the peroxo-dicopper(II) species [{Cu-II(
TMPA)}(2)(O-2(2-))](2+) (5) with m-chloroperoxybenzoic acid (m-CPBA);
hydrogen peroxide is a byproduct in this acid-base reaction. A trigona
l-bipyramidal mononuclear coordination in 1 is supported by W-vis and
EPR evidence, while a 1740 cm(-1) carbonyl infrared absorption suggest
s the percarboxylato ligand binds as a unidentate oxygen donor ligand.
Reaction of 1 with PPh(3) at -80 degrees C gives O=PPh(3) and the car
boxylato complex [Cu(TMPA)(m-ClC6H4C(O)-O-)](+) (6) (nu(c=0) = 1620 cm
(-1)). [Cu(Me(2)im)(3)(m-ClC6H4C(O)OO-)](+) (2; Me(2)im = 1,2-dimethyl
imidazole) is formed by reaction of m-CPBA with the peroxo-dicopper(II
) species [Cu-2(Me(2)im)(6)(O-2)](2+) (8) in CH2Cl2 at -90 degrees C.
Solution and solid-state spectroscopic data are consistent with a mono
nuclear formulation while nu(c=0) = 1745 cm(-1) also suggests terminal
percarboxylato coordination. While 1 and 2 are stable at room tempera
ture as solids, [Cu-II(CPY2-O-)(m-ClC6H4C(O)OO-)] (3; CPY2-OH = -(2-py
ridyl)ethyl][(2-hydroxyphenyl)methyl]-amine) is not. Is was generated
by reaction of [Cu(CPY2-O-)(Cl)] . 2H(2)O (9) with m-CPBA at -75 degre
es C. At this temperature, a 1750 cm(-1) IR absorption is ascribable t
o a coordinated perbenzoato ligand. Species 3 is the most reactive of
the three Cu((II)-percarboxylato complexes. Addition of PPh(3) (-80 de
grees C) causes a rapid change, giving O=PPh(3) and the carboxylato co
mplex [Cu(CPY2-O-)(m-ClC6H4C(OO-)] (10), which was independently synth
esized. Percarboxylato complexes 1 and 2 possess enhanced reactivity r
elative to peroxo-copper(II) complexes with the same ligands, a furthe
r example illustrating how electrophilic activation (e.g. by protonati
on or, here, by acylation) of peroxo groups leads to oxygen atom trans
fer functionality.