Thiodiacetato-copper(II) chelates with or without N-heterocyclic donor ligands: molecular and/or crystal structures of [Cu(tda)]n, [Cu(tda)(Him)2(H2O)] and [Cu(tda)(5Mphen)] · 2H2O (Him = imidazole, 5Mphen = 5-methyl-1,10-phenanthroline)

Three new thiodiacetato-Cu(II) chelates have been synthesized and studied by X-ray crystallography and by thermal, spectral and magnetic methods. [Cu(tda)]n (1) is a 3D-polymer with a pentadentate tda, which acts with a fac-O2 + S(apical)-tridentate chelating conformation and as a twofold anti, syn-μ–η1:η1 carboxylate bridge. In its square pyramidal Cu(II) coordination (type 4 + 1) four O(carboxylate) donors define a close regular square base, but the Cu–S(apical) bond deviates 27.4° from the perpendicular to the mean basal plane. Each anti,syn-bridging carboxylate group exhibits two C–O (average 1.26(1) Å) and two Cu–O bonds (average 1.958(7) Å), which are very similar in length to each other. In contrast, the mixed-ligand complexes of [Cu(tda)(Him)2(H2O)] (compound 2, distorted octahedral, type 4 + 1 + 1) and [Cu(tda)(5Mphen)] · 2H2O (compound 3, distorted square pyramidal, type 4 + 1) have molecular structures and the tda ligand displays only a fac-O2 + S(apical)-tridentate conformation. The Cu–S(apical) bond lengths (2.570(1), 2.623(1) or 2.573(1) Å for 1, 2 or 3, respectively) are shorter than those previously reported for closely related Cu(II)–tda derivatives. The different tda ligand roles in their Cu(II) derivatives are rationalized on the basis of crystal packing forces driving in the absence or presence of auxiliary ligands (with two or three N-donor atoms).

Graphical abstractThree new thiodiacetato-Cu(II) chelates are reported. In [Cu(tda)]n a pentadentate tda is found, with fac-O2 + S(apical) tridentate chelating conformation and twofold anti syn-μ–η1:η1 carboxylate bridging ligand role. Both bridges represent pairs of very similar C–O and Cu–O bonds. In contrast, [Cu(tda)(Him)2(H2O)] and [Cu(tda)(5Mphen)] · 2H2O only have tda in fac-O2 + S(apical) tridentate chelating conformation.Figure optionsDownload full-size imageDownload as PowerPoint slide