A new CuII complex with a diazamesocyclic ligand based on 1,4-diazacycloheptane (DACH) and functionalized with two additional quinoline donor groups, namely N,N-bis(quinolin-8- ylmethyl)-1,4-diazacycloheptane L, has been synthesized and characterized. X-ray diffraction analysis at room temperature indicates that the title complex [CuLCl](ClO4) 1 (C25H26Cl2N4O4Cu, Mr = 580.94) crystallizes in triclinic, space group P1 with a = 9.589(3), b = 10.857(4), c = 12.724(5) ? a = 98.168(7), b = 106.945(7), g = 101.248(7), V = 1214.6(8) 3, Z = 2, Dc = 1.588 g/cm3, F(000) = 598 and m(MoKa) = 1.161 mm-1. The final R = 0.0479 and wR = 0.0985 with 4267 independent reflections. In the mononuclear CuII complex, the CuII center is pentacoordinated to four nitrogen donors of the ligand and one axial chloride anion, taking a coordination sphere in the midst of the ideal square- pyramid and trigonal bipyramid.
A mononuclear complex, cis-[meso-1, 3-bis(propylsulfinyl)propane]- dichloroplatinum(Ⅱ) (Pt(C9H20O2S2)Cl2) 1, has been prepared and structurally characterizated by single-crystal X-ray diffraction. The crystal belongs to orthorhombic system, space group Pna21 with a = 22.800(3), b = 11.7662(13), c = 5.8115(6) ? V = 1559.0(3) ?, Mr = 490.36, Dc = 2.089 g/cm3, Z = 4, F(000) = 936, m (MoKa) = 9.596 mm-1 and l = 0.71073 ? The structure was refined to R = 0.0204 and wR = 0.0473 for 2703 reflections with I > 2(I). It is revealed that the central Pt(Ⅱ) ion in the title complex is bonded to two Cl atoms in a cis-configuration and two S atoms of the ligand to form the coordination geometry deviating slightly from the square planar.
The complex Cu(phon)(NO3)2(CH3CN) (phon = 1,10-phenanthroline-5,6-dione) has been synthesized and characterized by elemental analysis, infrared and UV-Vis spectra. X-ray diffraction analysis at room temperature indicates that the complex crystallizes in orthorhombic system, space group P212121 with a = 8.353(1), b = 11.299(2), c = 17.764(2) A, V= 1676.5(4) A3, Z = 4, C14H9CuN5O8, Mr = 438.8, Dc = 1.739 g/cm3, F(000) = 884 and μ(MoKα) = 1.361 mm-1. The final R and wR factors for the observed reflections with I > 2σ(I) are 0.0353 and 0.0855, respectively. R = 0.0432 and wR = 0.0899 for all data. The structure of the title complex consists of a neutral mononuclear entity. The central Cu (II) atom is five-coordinated by two nitrogen donors of one ligand, two unidentate NO3- ions and one CH3CN molecule. The coordination geometry of Cu (II) can be considered as a distorted trigonal bipyramidal configuration. The complex ability of the NO3-ion has more effect than that of the ClO4- ion on the structure of the complex.
The title complex was prepared from the reaction of 1,2-bis(phenylthiomethyl)- benzene L with K2PtCl4 at room temperature and its structure has been determined by single-crystal X-ray diffraction. There exist two independent cis-[1,2-bis(phenylthiomethyl)benzene]dichloro- platinum(Ⅱ) [PtCl2L] molecules without significant structural difference and a molecule of acetonitrile in one crystallographic asymmetric unit. Crystallographic data: triclinic, space group Pī, a = 11.010(3), b = 12.080(3), c = 16.095(4) ? = 94.728(5), = 90.129(5), = 99.274(5)? C20H18Cl2NPtS20.5CH3CN, Mr = 608.98, V = 2105(1) ?, Z = 4, Dc = 1.921 g/cm3, (Mo-K) = 7.122 mm1, F(000) = 1172, R = 0.0503 and wR = 0.0848 for 3929 observed reflections with I > 2s(I). The title complex is a neutral molecule in which the central Pt(Ⅱ) ion is four-coordinated with two S-donors of the ligand and two Cl anions, forming a distorted square planar geometry. In the crystal, there exist two kinds of molecular packing patterns. One [PtCl2L] molecule is connected to the other one through the weak interactions of Pt…Pt, Pt…S and Pt…Cl, forming a supramolecular quasi-dimer. The other one complex molecule is connected with the CH3CN molecule by weak Cl…N interaction.
The diprotonated perchlorate salt of 2,3-di-2-pyridyl-5-nitroquinoxaline [C18H13N5O2](ClO4)2·(CH3OH)·(C2H5OH) has been synthesized and characterized by elemental analysis, IR and NMR spectra. X-ray diffraction analysis at room temperature indicates that the title compound (C21H23N5O12Cl2, Mr = 608.34) crystallizes in triclinic, space group P 1 with a = 7.992(8), b = 12.82(1), c = 13.42(1) A, α = 104.77(2),β = 97.84(2), r= 95.48(2)°, V= 1305(2) A3, Z = 2,DC= 1.549 g/cm3, F(000) = 628 and μ(MoKα) = 0.317 mm-1. The final R and wR factors are 0.0566 and 0.1016, respectively with 4325 independent reflections. The quinoxaline ring makes the dihedral angles of 44.2(2) and 33.9(5)° with two protonated pyridine rings whose dihedral angle is 48.1(6)°. The favored orientation of two protonated pyridine rings is that thek N atoms are opposite to each other. There exist intra- and inter-molecular N-H…O hydrogen bonds and π…π interactions which stabilize the structure further.
