Three water-soluble silver(I) complexes, i.e., {[Ag(S-othf)](2)}(n) 1, {[Ag(R-othf)](2)}(n) 2 and {[Ag-2(R-othf)(S-othf)]}(n) 3 (S- and R-Hothf = (S)-(+)- and (R)-(-)-5-oxo-2-tetrahydrofurancarboxylic acid, respectively), showing effective antibacterial and antifungal activities, have been synthesized and their crystal structures determined. Single-crystal X-ray analysis revealed that 1 and 2 in the solid state are a left- and a right-handed chiral helical polymer, respectively, formed by self-assembly of non-centrosymmetric, bis-carboxylato-bridged bis(carboxylato-O,O')disilver dimers (Ag-Ag distances 2.822(1) Angstrom for 1 and 2.823(2) Angstrom for 2; O-Ag-O angles 164.0(2), 155.2(2)degrees for 1 and 163.8(3), 154.5(3)degrees for 2). The helicity of 1 and 2 in the solid state is accomplished with a connection of one oxo group in one dimeric core to one of the silver(I) centers of the adjacent dimeric unit and also with simultaneous connection of one of the carboxylato oxygens to the silver(I) center of a different dimer. These bonding modes are quite different from those of the stair-like polymer 3 formed by self-assembly of the dimeric core (Ag-Ag 2.781(1) Angstrom; O-Ag-O angle 164.8(1)degrees). Crystals of 3 with achiral polymer structure were identical with those of 4 obtained from an aqueous solution containing equal amounts of 1 and 2, evidencing the presence of a ligand replacement between 1 and 2 in aqueous solution. The complexes 1-3 have also been characterized by elemental analysis, TG/DTA, FT-IR, and H-1 and C-13 NMR spectroscopies. The wide spectra of effective antibacterial and antifungal activities observed in 1-3 suggested that the weaker silver(I)-O bonding properties play a key role in the antimicrobial activities.