A new mixed complex [Zn(tren) (H-SSA)] was synthesized based on the reaction of ZnO,5-sulfosalicylic acid and tren in water-methanol mixed solvents where tren was tris(2-aminoethyl)amine for the first time. The structure of the mixed complex was characterized by elemental analysis, IR, 1H NMR and thermal analysis. The crystal structure of the complex was also determined by X-ray single crystal diffraction. Its crystal belongs to trigonal system with space group P31, a=1.109 67(18) nm, b=1.109 67(18) nm, c=1.236 8(4) nm, V=1.318 9(5) nm3; Dc=1.616 g·cm-3; Z=3; F(000)=666; μ=1.553 mm-1. CCDC: 253908.
The complex [Zn(acac)2(C5H4NOH)] was synthesized based on the reaction of zinc(Ⅱ)acetate,acetylaceton and 3-hydroxypyridine(C5H4NOH)in methanol medium.The structure of the complex was confirmed by IR,1H NMR,elemental analysis,thermal analysis and X-ray single crystal diffraction.The crystal belongs to monoclinic system with space group P21/n,and a=0.743 7(3)nm,b=0.829 5(3)nm,c=2.612 5(9)nm,β=95.026(6)°,V=1.605 4(9)nm3;Dc=1.484 g·cm-3;Z=4;F(000)=744;μ=1.551 mm-1.Zinc(Ⅱ)atom lies at the center of an coordination of the distorted square pyramidal formed by four O atoms which come from two different acetylaceton ions and one N atom from the 3-hydroxypyridine molecule.CCDC:600232.
A mixed complex [Zn(CF3COO)2(C7H6NS)2] was synthesized based on the reaction of Zn(CF3COO)2 and 2-aminobenzothiazol (C7H6NS) in methanol. The structure of the complex was characterized by elemental analysis, IR, 1H NMR and thermal analysis. The crystal structure of the complex was determined by X-ray single crystal diffraction. The crystal belongs to monoclinic system with space group C2/c, a=3.174 3(9) nm, b=1.010 0(3) nm, c=1.723 1(5) nm, β=118.841(4)°, V=4.839(2) nm3; Dc=1.625 g·cm-3; Z=8; F(000)=2 368; μ=1.266 mm-1. CCDC: 600233.
