Complexation of copper(II) by calixarene-based ligands bearing either two or three N-benzylimidazole coordinating arms under basic conditions has been studied. Whereas the tris(imidazole) derivative stabilizes dicationic 5-coordinate aqua complexes in a mononuclear state with an intracavity bound guest, in the presence of hydroxide ions, the latter undergo dimerization. An X-ray structure revealed decoordination of one imidazole arm and formation of a bis(hydroxo) bridged Cu(II) core with a square-planar geometry for both metal centers sandwiched by two empty calixarene cavities. Upon methanolysis, the dinuclear complex underwent an unexpected rearrangement leading to the clean formation of a trinuclear complex. X-ray diffraction analyses of this novel species revealed a trinuclear core constructed around a central Cu(II) ion that is doubly bridged through either methoxide or hydroxide anions to two Cu(II) ions hold by two calixarene units. The same complex could be directly synthesized by reacting the ligand with copper(II) perchlorate in a 2:3 ratio in the presence of base. In solution, the tetrahydroxo Cu-3 complex was characterized by UV-vis and H-1 NMR spectroscopies and displayed an electron paramagnetic resonance (EPR) signal only below 100 K that accounts for a S = 1/2 fundamental state. Formation of the same di- and trinuclear species was observed with a calixarene-based bis(imidazole) ligand, which demonstrates the generality of the reaction schemes. All these results emphasize the versatility of the calixarene scaffold for the stabilization of metal complexes with various nuclearities.