Substitution reactions of anhydrous copper(II) acetate with some higher car
boxylic acids and hydroxycarboxylic acids were carried out in toluene under
reflux. The isolated products; Cu(OOCR)(OOCR'), Cu(OOCR)(OOOCR ") and Cu(O
OCR)(OOCR''') [where R = C13H27, C17H35 or C21H43 and R' = C6H4OH, R " = C6
H5CH(OH) and R''' = (C6H5)(2)C(OH)] were characterized by elemental analyse
s, spectral (infrared and electronic) analyses and conductivity measurement
s. IR spectra suggest the presence of bidentate-bridging coordination of ca
rboxylate anions in the complexes. Magnetic moment measurement and electron
spin resonance spectral data suggest antiferromagnetic coupling between tw
o copper atoms. The dinuclear nature of the complexes was confirmed by mole
cular weight determinations.