Abstract

Reaction of acetylacetone (Hacac) with aldehyde (RCHO; R =p-MeOC6H4, p-ClC6H4 or Ph) in 2 : 1 mol ratio resulted in the formation of new triketones (HL2), which were previously characterized as bis(β-diketones) of the type [(MeCO)2CHCHRCH(COMe)2](H2L1). Mixed-ligand copper(II) complexes with N,N,N′,N′-tetramethylethane-1,2-diamine (tmen) and the β-diketonate moiety of these triketones, [CuCl(L2)(tmen)], were synthesized and their solvatochromic properties in organic solvents (due to the acceptor properties of the solvent) investigated. The colour of these five-co-ordinated complexes in the solid state gradually changes from green in [CuCl(L2)(tmen)] through bluish green, [CuCl(L2)(tmen)]·CH2Cl2, to blue, [CuCl(L2)(tmen)]·MeOH·CH2Cl2. Crystallographic studies showed that this phenomenon arises from an intermolecular hydrogen bond between the co-ordinated chloride of one complex and the OH group of a triketonate ligand of an adjacent complex and/or cocrystallized MeOH molecule.

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