Two helical centrosymmetric homotetranuclear Cu (II) complexes, [Cu 4 (L) 2 (EtOH) 2 ](ClO 4 ) 2 Á2EtOHÁ2CHCl 3 (1) and [{Cu 4 (L) 2 (EtOH) 2 }{Cu 4 (L) 2 (HNO 3 ) 2 }] (NO 3 ) 4 Á3EtOHÁ3MeOH (2), were synthesized by the reactions of a symmetric bis (salamo)-based ligand H 3 L with Cu(ClO) 2 Á6H 2 O and Cu(NO) 3 Á3H 2 O, respectively, and certified by elemental analyses, UV-Visible absorption spectra, infrared spectra and single-crystal X-ray analysis techniques. X-ray crystal structure analyses reveal that four Cu (II) atoms of complex 1 are attached to two deprotonated ligand (L) 3À units with the help of two coordinated ethanol molecules, and then forming a helical centrosymmetric complex by H-bonding and πÁ Á Áπ interactions. While complex 2 unit cell contains two crystallographically independent but chemically identical homotetranuclear complexes (molecules A and B), eight Cu (II) atoms are coordinated by four deprotonated ligand (L) 3À units. The coordination mode of four Cu (II) atoms from molecule A is the same as complex 1; at the same time, oxygen atoms on nitrates are involved in the coordination of another four Cu (II) atoms from molecule B. The short-range interactions in complexes 1 and 2 were calculated by Hirshfeld surfaces analyses. The molecular orbital energy levels, molecular stabilities of complexes 1 and 2 were analyzed by DFT calculations. In addition, antibacterial assays were also investigated in detail.