Copper(II)-Assisted Ligand Fragmentation Leading to Three Families of Metallamacrocycle.

ABSTRACT

We present an unprecedented copper(II)-assisted organic ligand fragmentation process under basic conditions leading to several ligands within three families of metallamacrocycle, Cu6, Cu8, and Cu16. The sequential multistep reaction include (i) the deprotonation of the starting alcohol, 1,2-bis(3,5-dimethyl-pyrazol-1-yl)ethane-1,2-diol (H2bdped) to its diolate bdped followed by complexation through six bonds (µ6) to three copper atoms in a ring, (ii) the breaking of the ethane-pyrazole C-N bonds by the different solvent alcohols to form 1-(3,5-dimethyl-pyrazol-1-yl)-2-methoxyethane-1,2-diolate (dpmed) or 2-(3,5-dimethyl-pyrazol-1-yl)-2-hydroxyacetate (dpet), while retaining coordination to the copper centers and (iii) the final step to ethane-1,1,2,2-tetraolate, C2H2O44- (et). Importantly, the latter product, only observed on two previous occasions, occupies the core of Cu6 and Cu16 through exceptionally eight coordination bonds (µ8). Its alkyl esters, 2-alkoxyethane-1,1,2-triolate (met, eet, and pet), also occupy the central parts of Cu8 but forming six bonds (µ6) instead. The other product, 3,5-dimethylpyrazolate (dp), acts as peripheral bridges (µ2) but it is not involved in coordination if the starting salt is copper acetate, this may be a consequence of acetate being a better µ2-chelating ligand. In the presence of an oxidizing agent, K2Cr2O7, C2H2O44- (et) is oxidized to oxalate, C2O42- (ox). Thus, an additional µ3-hydroxide and µ4-oxalate in Cu16 widen the complexity of the structures, not to mention the range of coordination geometries of the copper centers, though in the present cases they can be classed in only two types distorted square-planar and square-pyramid. In addition to single-crystal crystallography, the results from different techniques such as IR, ESI-MS, optical UV-vis, and SQUID magnetometry help in the characterization of these rare metallamacrocycles made from unexpected and in situ generated ligands. We believe the results of the organic transformations are highly relevant to von Liebig's benzil-benzilic acid rearrangement.