Cubane-like tetranuclear Cu(ii) complexes bearing a Cu4O4 core: crystal structure, magnetic properties, DFT calculations and phenoxazinone synthase like activityElectronic supplementary information (ESI) available: Crystal refinement parameters (Table S1), selected bond lengths and angles (Table S2), change in the spectral pattern (Fig. S1), rate vs. substrate concentration and Lineweaver-Burk plots (Fig. S2), χT vs. T dependence (Fig. S5), and Cartesian coordinates of the theoretical calculated

In the present work, two new copper complexes 3a and 3b with a Cu 4 O 4 cubane core are reported. Both complexes are obtained by means of the in situ conversion of the imine functionality of Schiff's base ligands 1a [( E )-4-chloro-2-((thiazol-2-ylimino)methyl)phenol] and 1b [( E )-4-bromo-2-((thiazol-2-ylimino)methyl)phenol] into amino alcohols 2a (4-chloro-2-(hydroxy(thiazol-2-ylamino)methyl)phenol) and 2b (4-bromo-2-(hydroxy(thiazol-2-ylamino)methyl)phenol), respectively. The ligand transformation may be metal assisted and the generated ligands show an interesting mode of coordination in which the alkoxo-O atom binds in a μ 3 -manner connecting simultaneously three copper centers and forming a Cu 4 O 4 cubane core. The first analysis of single crystal X-ray diffraction studies reveals that both molecules possess a [4 + 2] cubane-type core, and low temperature magnetic measurements show antiferromagnetic behaviour, in agreement with DFT calculations. However, the best fit and DFT calculations point out three pairs of coupling constants, more coherent with a [2 + 2 + 2] situation, in accordance with the fine analysis of structural data. Finally, phenoxazinone synthase activity has been measured for both molecules, finding k cat = 86.3 h −1 for the chloride derivative copper( ii ) complex in methanol, whereas the bromide derivative copper( ii ) complex displays k cat = 3.4026 × 10 2 h −1 and 10.289 × 10 2 h −1 in methanol and DMSO, respectively. Two tetranuclear copper complexes with a Cu 4 O 4 cubane core exhibiting phenoxazinone synthase like activity are reported.