作者:Jonathan D. Crane、David E. Fenton、Jean Marc Latour、Arnold J. Smith
DOI:10.1039/dt9910002979
日期:——
Dicopper(II) complexes of unsymmetrical dinucleating Schiff-base ligands bearing chemically distinct co-ordination sites have been prepared and their properties studied. The ligands were derived from the condensation of 4-bromo-2-formyl-6-(4-methylpiperazin-1-ylmethyl)phenol and 4-bromo-2-[(2-diethylaminoethyl)ethylaminomethyl]-6-formylphenol with 2-(aminomethyl)pyridine, 2-(2-aminoethyl)pyridine,
Copper coordination to the aldehyde and hemiacetal form of 4-bromo-2-[(2-diethylaminoethyl)ethylaminomethyl]-6-formylphenol: Synthesis and structure of [Cu(H2L)2(X)2] X2·nH2O () and [Cu(L′)]2·2CH3OH
作者:Andrea Erxleben
DOI:10.1016/j.ica.2008.02.016
日期:2009.2
The coordination behaviour of Cu2+ towards 4-bromo-2-[(2-diethylaminoethyl)ethyl-aminomethyl]-6-formylphenol(HL) having phenolate, amine and aldehyde donor sites has been studied. In aqueous, weakly acidic solution Cu2+ coordinates to the phenolate and aldehyde oxygen giving rise to the complexes [Cu(H2L)(2)X-2]X-2 (X = NO3- (1a) and CIO4- (1b)), while in alkaline solution a complex of composition [CuL2] (2) is formed. In methanol, the aldehyde groups in 1 and 2 suffer nucleophilic attack from the solvent resulting in the formation of the hemiacetal form of the ligand and in the isolation of [Cu(L')](2) center dot 2CH(3)OH (3). X-ray structures of 1a, 1b and 3 are reported, the latter featuring a rare example of a coordinated methyl-hemiacetal. (C) 2008 Elsevier B. V. All rights reserved.