NEW COPPER(I) HALIDE-COMPLEXES WITH 2,2'-DIPYRIDYLAMINE AND PRODUCTS OF THEIR AUTOXIDATION - X-RAY-DIFFRACTION STRUCTURE OF A TRIPLY-BRIDGED MU-CL-MU-(OME)(2)-DICOPPER(II) COMPLEX
N. Marsich et al., NEW COPPER(I) HALIDE-COMPLEXES WITH 2,2'-DIPYRIDYLAMINE AND PRODUCTS OF THEIR AUTOXIDATION - X-RAY-DIFFRACTION STRUCTURE OF A TRIPLY-BRIDGED MU-CL-MU-(OME)(2)-DICOPPER(II) COMPLEX, Inorganica Chimica Acta, 236(1-2), 1995, pp. 117-124
Some new complexes of Cu(I)X (X = Cl, Br, I) with 2,2'-dipyridylamine
(dipyam) have been prepared and their autoxidation in methanol has bee
n investigated. The products were characterized by elemental analysis
and IR spectroscopy. The X-ray diffraction structure of the [Cu-2(mu-O
Me)(2)(mu-Cl)dipyam(2)]Cl . MeOH (10) complex is reported. Crystals of
10 are orthorhombic, space group Cmc2(1), with a = 14.993(5), b = 8.1
91(4), c = 21.237(6) Angstrom, Z = 4, and R = 0.052 for 1482 observed
independent reflections. In the dinuclear monocations the triply-bridg
ed Cu(II) ions show a distorted square-pyramidal coordination with fou
r short in-plane bonds involving two N atoms from a terminal dipyam li
gand and two O atoms from two bridging methoxy groups. The fifth apica
l ligand is a longer bonded bridging chloride ion, which joins the bas
al CuN2O2 planes in a roof-top configuration.