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Five new tetradentate unsymmetrical ligands, ethylene-N-(acetylacetoneimine)-N′-(ortho-hydroxyl arylaldimine) (aryl = 3,5-dibromophenyl, 3-methylphenyl, 3,6-dimethylphenyl, 3,5-dichlorophenyl, 3,5-dibromoacetophenone), have been prepared and characterized for studies of the general structure of their copper(II) complexes and assessment of the substituent effects on central metal ions. Upon reaction with copper(II) ions, the ligands derived from aryls, where aryls are 3,5-dibromophenyl, 3-methylphenyl, 3,6-dimethylphenyl and 3,5-dibromoacetophenone, give the corresponding copper(II) complexes while the ligand derived from 3,5dichlorophenyl undergoes partial hydrolysis leading to the cleavage of an acetylacetone moiety. The general coordination configuration has been revealed by an X-ray crystallographic study of one of the complexes, ethylene-N-(acetylacetoneiminato)-N′-(o-hydroxy-3,5-dibromoacetophenoneiminato)copper(II), which exhibits an approximately square-planar geometry with a slight tetrahedron distortion. An ESR study of the copper(II) complexes in solution indicates electronic effects from substituents influence the reactivity of central metal ions. In addition, a key step in preparation of the unsymmetrical ligands has been dramatically improved to ensure synthetic reproducibility and eliminate the decomposition of an intermediate, 7-amino-4-methyl-5azo-3-heptene-2-one, AMAHO. Thermal stability of the complexes has been also evaluated to assess the compatibility of the two donating moieties.

Eight new vanadyl complexes utilizing unsymmetrical bis-Schiff base ligands [VOL, H 2 L = o -HOArC(R)NCH 2 CH 2 NHC(CH) 3 )CHC(O)CH 3 ], prepared from ethylene-diamine, acetylacetone and a salicylaldehyde derivative have been synthesized and characterized. A 0 and g 0 values determined by ESR were found to be solvent-independent. Substituents on the phenyl ring of the ligand strongly effect A 0 , with strongly electron-withdrawing groups giving rise to higher A 0 values, however, g 0 was only slightly effected by ring substituents. VO[2-O-3,5-Br 2 C 6 H 2 C(CH 3 )NCH 2 CH 2 NC(CH 3 )CHC(O)CH 3 (VOL 8 ) was characterized by single-crystal X-ray crystallography and the vanadium was found to be displaced above the basal plane by 0.612 A. This large displacement of the vanadium from the basal plane may contribute to solvent-independence of A 0 and g 0 values determined by ESR.

A modified method for the synthesis of o-hydroxyaryl aldehydes in moderate yields has been developed by treating aryloxymagnesium bromides with formaldehyde using triethylamine in place of hexamethylphosphoric triamide (HMPA).

A modified method for the synthesis of o-hydroxyaryl aldehydes in moderate yields has been developed by treating aryloxymagnesium bromides with formaldehyde using triethylamine in place of hexamethylphosphoric triamide (HMPA).