Investigation of structural characteristics of bis(beta-diketonato)copper(II) complexes containing alkoxy or aryloxy side chains: X-ray structures of1,3-bis(4-butoxyphenyl)propane-1,3-dione, bis[1,3-bis(4-butoxyphenyl)propane-1,3-dionato-kappa O,kappa O ']copper(II) and bis[1,3-bis(4-phenoxyphenyl)propane-1,3-dionato-kappa O,kappa O ']copper(II)
Ja. Campo et al., Investigation of structural characteristics of bis(beta-diketonato)copper(II) complexes containing alkoxy or aryloxy side chains: X-ray structures of1,3-bis(4-butoxyphenyl)propane-1,3-dione, bis[1,3-bis(4-butoxyphenyl)propane-1,3-dionato-kappa O,kappa O ']copper(II) and bis[1,3-bis(4-phenoxyphenyl)propane-1,3-dionato-kappa O,kappa O ']copper(II), HELV CHIM A, 84(8), 2001, pp. 2316-2329
Copper(H) complexes containing beta -diketonato ligands of the general form
ula [Cu{(4-RO)C6H4COCHCOC6H4(4-OR))(2)] 3 (R = Bu) or 4 (R = Ph) were prepa
red and their structures solved by X-ray diffraction. The crystal structure
of the parent ligand (4-BuO)C6H4COCH2COC6H4(4-OBu) 1 was also solved, The
influence of the different side chains 4-RO-C6H4 (R = Bu or Ph) on potentia
l liquid-crystal properties was investigated for both the ligands and the c
opper derivatives. The presence of BuO substituents at the aromatic rings a
ppears to improve the molecular linearity with respect to 1,3-diphenylpropa
ne-1,3-dione (=dibenzoylmethane; DBM), this feature being of interest for r
od-like structures. On the other hand, the molecular structure of the coppe
r(II) complexes 3 and 4 showed a flat core almost unmodified by the differe
nt peripherical substituents, A columnar arrangement was observed for both
compounds 3 and 4, but, additionally, a layer-like disposition was also fou
nd in 3, which was proved to be a metallomesogen.