Abstract: | Two novel one‐ and two‐dimensional network structure bismuth(III) complexes with N, N‐di(2‐hydroxylethyl)‐aminodithiocarboxylate, {BiS2CN(C2H4OH)2]21, 10‐Phen]2(NO3)}·3H2O (1) and (BiS2CN(C2H4OH)2]3)2 (2) were synthesized. Their crystal and molecular structures were determined by X‐ray single crystal diffraction analysis. The crystal 1 belongs to monoclinic system with space group C2/c, a=1.6431(7) nm, b=2.4323(10) nm, c= 1.2646(5) nm, β=126. 237(5), Z=4, V=4.076(3) nm3, Dc=1.757 Mg/m3, μ=4.598 mm?1, F(000)=2156, R= 0.0211, wR=0.0369. The structure shows a distorted square antiprism configuration with eight‐coordination for the central Bi atom. The one‐dimensional chain structure was formed by H‐bonding interaction between hydroxyl group of N, N‐di(2‐hydroxylethyl)aminodithiocarboxylate ligands and crystal water. The crystal 2 belongs to monoclinic system with space group p2(1)/c, a= 1.1149(4) nm, b=2.1274(8) nrn, c=2.2107(8) nm, β=98.325(8)°, 2=4, V=5. 188(3) nm3, Dc=1.920 Mg/m3, μ=7.315 mm?1, F(000)=2944, R=0.0565, wR=0.0772. The structure shows a distorted square antiprism configuration with eight‐coordination for the central Bi atoms. The two‐dimensional network structure was formed by H‐bonding interaction between adjacent molecules. |