In the crystal structure of the title compound, [Cu(2)(C(2)H(3)O(2))(4)(C(12)H(12)N(2))(2)], the binuclear mol-ecule lies about a center of inversion; the four acetate groups each bridge a pair of Cu(II) atoms. The coordination of the metal atom is distorted square-pyramidal, with the bonding O atoms comprising a square basal plane and the coordinating N atom of the N-heterocycle occupying the apical position. The pyridine ring is twisted with respect to the benzene ring at a dihedral angle of 45.68 (16)°. Intra-molecular N-H⋯O hydrogen bonding is present between the imino and carb-oxy groups.
In the centrosymmetric title mol-ecule, [Cu(2)(CH(3)COO)(4)(C(6)H(9)N(3))(2)], each of the four acetate groups bridges a pair of Cu(II) atoms [Cu-Cu = 2.6540 (4) Å]. The distorted octa-hedral geometry of the metal atom is completed by an N-donor atom of the N-ethyl-pyrimidin-2-amine ligand: an intra-molecular N-H⋯O hydrogen links its N-H group to an acetate carboxyl-ate O atom. In the crystal, C-H⋯O inter-actions link the mol-ecules into a supra-molecular chain along the b axis.
The central Cd(II) atom in the trinuclear title compound, [Cd(3)(C(14)H(19)N(2)O(3))(2)(CH(3)COO)(4)], lies on a center of inversion and is bonded to the O atoms of four acetate groups as well as to the phenolate O atoms of the mono-deprotonated Schiff base ligands in a distorted all-trans octa-hedral geometry. Two of the acetate groups function in a μ(2)-bridging mode, while the other two each chelate to the terminal Cd(II) atom and simultaneously bind to the central metal atom in a κ(3)-bonding mode. The Schiff base anions N,O-chelate to the terminal metal atoms. The morpholine ring assumes a chair conformation.
The structure of the dinuclear title complex, [Cu(2)(C(5)H(9)O(2))(4)(C(5)H(5)N)(2)], represents a monoclinic polymorph of the previously reported triclinic form [Blewett et al. (2006 ▶). Acta Cryst. E62, m420-m422]. Each carboxyl-ate group is bidentate bridging and the distorted octa-hedral geometry about each Cu(II) atom is completed by a pyridine N atom and the other Cu atom [Cu⋯Cu = 2.6139 (7) Å]. In the crystal, mol-ecules are connected into supra-molecular chains via π-π inter-actions formed by the pyridine rings [centroid-centroid distance = 3.552 (3) Å] and these are connected into a two-dimensional array in the ac plane by C-H⋯π contacts. One of the tert-butyl groups is disordered over two orientations in a 0.734 (6):0.266 (6) ratio.
In the title solvated salt, [Ag(C18H15P)4](CF3CO2)·C2H5OH, the Ag(I) atom is coordinated by four P atoms from triphenyl-phosphane ligands in a distorted tetra-hedral geometry. The anion and solvent are engaged in weak O-H⋯O hydrogen bonds. Of the four triphenyl-phosphane ligands, two each have an equally disordered phenyl ring while the Ag(I) atom is disordered over two positions in a 0.9595 (15):0.0405 (15) ratio and the trifluoro-acetate anion is equally disordered over two positions with respect to the lattice ethanol mol-ecule.
The Ag(I) atom in the title hydrated solvated salt, [Ag(C18H15As)4](CF3CO2)·0.5CH3OH·0.5H2O, is coordinated by four As atoms from triphenyl-arsane ligands in a distorted tetra-hedral geometry. In the crystal, O-H⋯O hydrogen bonding occurs between carboxyl-ate groups of anions and lattice solvent mol-ecules. Of the four triphenyl-arsane ligands in the Ag complex cation, two each have an equally disordered phenyl ring while the trifluoro-acetate anion is disordered over two positions with respect to the lattice methanol and water mol-ecules which both show half-occupyncy. The crystal studied was a non-merohedral twin with a 13.6 (1)% contribution of the minor twin component.
The mol-ecule of the title compound, [Sn(C(5)H(5)S)(4)], lies on a special position of site symmetry. The Sn(IV) atom shows a slightly distorted tetra-hedral coordination.
The six-coordinate Sn(IV) atom in the title compound, [SnCl(4)(C(14)H(14)OS)(2)], exists in a cis-SnCl(4)O(2) octa-hedral geometry. Of the four Cl atoms, two are close to adjacent S atoms [Cl⋯S = 3.320 (1) and 3.376 (1) Å]; the Sn-Cl bonds involving these two Cl atoms are longer than the other two Sn-Cl bonds.
In the title salt, C(7)H(11)N(2) (+)·Br(3) (-), the essentially planar cation (r.m.s. deviation = 0.006 Å) forms an N-H⋯Br hydrogen bond to one of the Br atoms of the almost linear anion [Br-Br-Br = 179.31 (2)°]. The crystal studied was found to be a racemic twin. The whole-mol-ecule disorder of the cation and anion about a twofold rotation axis described earlier [Ng (2009). Acta Cryst. E65, o1276] is an artifact of halving one of the axes of the ortho-rhom-bic unit cell.
3,6,11-trihy-droxy-1,1-dimethyl-2,3-di-hydro-chromeno[2,3-f]chromen-7-one monohydrate), known as pruniflorone N, crystallized as a monohydrate, C18H16O6·H2O. The three ring systems of the xanthone skeleton are approximately coplanar, with an r.m.s. deviation of 0.0270 (1) Å from the plane through the 14 non-H atoms. The O atoms of the two hy-droxy substituents on the benzene rings also lie close to this plane, with deviations of 0.019 (1) and 0.070 (1) Å. The 2'-hy-droxy-4',4'-di-methyl-pyran ring is disordered over two positions with a 0.798 (3):0.202 (3) site-occupancy ratio. An intra-molecular O-H⋯O hydrogen bond generates an S(6) ring motif. In the crystal, the xanthone and water mol-ecules are linked into a three-dimensional network by O-H⋯O hydrogen bonds and weak C-H⋯O inter-actions. π-π inter-actions, with centroid-centroid distances of 3.5982 (7), 3.6081 (7) and 3.6456 (7) Å, are also observed.
The dihedral angle between the two aromatic ring systems in the title compound, C(15)H(12)N(2)O, is 42.6 (1)°. The angle at the O atom is widened to 117.7 (1)°.
The dihedral angle between the two aromatic ring systems in the title compound, C(15)H(12)N(2)O, is 85.9 (1)°; The angle at the O atom is widened to 118.2 (2)°. The quinoxalin-yloxy part of the mol-ecule lies on a mirror plane and the tolyl group is disordered over two positions about the mirror plane.
The dihedral angle between the two aromatic ring systems in the title compound, C(15)H(12)N(2)O, is 79.4 (1)°. The angle at the O atom is widened to 116.93 (9)°.
The asymmetric unit of the title compound, C(10)H(6)N(2)·0.5C(4)H(4)O(4), consists of one quinoline-2-carbonitrile mol-ecule and a half-mol-ecule of fumaric acid, which lies on an inversion center. The quinoline-2-carbonitrile mol-ecule is almost planar, with an r.m.s. deviation of 0.008 (1) Å. The acid and base are linked together via pairs of inter-molecular C-H⋯O and O-H⋯N hydrogen bonds, forming R(2) (2)(8) ring motifs. In the crystal, the carbonitrile mol-ecules are further linked by inter-molecular C-H⋯N hydrogen bonds, generating R(2) (2)(10) ring motifs, resulting in zigzag chains running along the c axis.
In the title compound, C(10)H(6)N(2), the mol-ecule is almost planar, with an r.m.s. deviation of 0.014 Å. The dihedral angle between the aromatic rings is 1.28 (16)°. In the crystal, mol-ecules are stacked along the a axis by way of weak aromatic π-π stacking inter-actions between the benzene and pyridine rings of adjacent mol-ecules [centroid-centroid separation = 3.7943 (19) Å].
The title compound, C(13)H(16)N(2)O(3)S, is a thio-urea derivative with benzoyl and propoxycarbonyl-methyl groups attached to the two terminal N atoms. These groups adopt trans and cis configurations, respectively, with respect to the S atom across the thio-urea C-N bonds. The compound crystallizes in the P2(1)/c space group with Z = 8, resulting in two unique molecules in the asymmetric unit linked by C-H⋯S and C-H⋯O hydrogen bonds, forming a one-dimensional zigzag chain along the c axis.
The V(V) atom in the polymeric title compound, [NaV(C(15)H(13)N(3)O(3))O(2)(H(2)O)(2)](n), is O,N,O'-chelated by the Schiff base dianion and is five-coordinated in a trigonal-bipramidal coordination geometry. The oxide O atoms occupy the equatorial sites and one oxide O atom is connected to the Na(I) atom. The ligand simultaneously O,O'-chelates to the water-coordinated Na(I) atom; its coordination number is seven owing to an Na⋯N(pyrid-yl) bond. The two independent formula units, which are disposed about a false center of inversion, are connected into a layer. Adjacent layers are consolidated into a three-dimensional network by O-H⋯O and O-H⋯N hydrogen bonds.
The title complex, [Cu{μ3-O2CC6H3(NO2)2-3,5}(μ-OH)] n , features zigzag chains in which successive pairs of Cu(II) atoms are connected by OH bridges and bidentate carboxyl-ate ligands, leading to six-membered Cu(O)(OCO)Cu rings. The zigzag chains are connected into a three-dimensional architecture by Cu-O(nitro) bonds. The coordination geometry of the Cu(II) atom is square-pyramidal, with the axial position occupied by the nitro O atom, which forms the longer Cu-O bond. Bifurcated hy-droxy-nitro O-H⋯O hydrogen bonds contribute to the stability of the crystal structure.
In the crystal structure of the title compound, [Fe(C(6)H(4)NO(2))(2)](n), one nicotinate group O,O'-chelates one Fe atom and binds through the N atom to the other Fe atom; the second nicotinate group bridges three Fe atoms through the N and two O atoms. The μ(2)- and μ(3)-bridging modes of the two nicotinate groups result in a polymeric three-dimensional network structure. The Fe atom shows octa-hedral coordination geometry but one of the Fe-O bonds is somewhat long [2.522 (2) Å].
The cyclo-hexane-1,3-dicarboxyl-ate dianion in the title three-dimensional coordination polymer, [Zn(2)(C(8)H(10)O(4))(2)(C(10)H(8)N(2))](n), has one carboxyl-ate group in an equatorial position and the other in an axial position of the cyclo-hexane ring, which adopts a chair conformation. The carboxyl-ate groups function as bridges to two adjacent Zn(II) atoms, generating a layer motif. Adjacent layers are linked through the 4,4'-bipyridine N-heterocycle, forming a three-dimensional network; the geometry of Zn(II) is square-pyramidal with the N atom of the N-heterocycle occupying the apical position. The N-heterocycle lies about a center of inversion and is disordered in a 1:1 ratio with respect to the C atoms bearing H atoms.