Jairo Bordinhao

1,3-Bis(4-nitrophenyl)triazene

The structure of the title compound, C(12)H(9)N(5)O(4), reveals an almost planar molecule (r.m.s. deviation = 0.061 A), in which the interplanar angle between the phenyl rings is 5.7 (1) degrees and the largest interplanar angle is that between the phenyl ring and the nitro group of one of the 4-nitrophenyl substituents [8.8 (3) degrees ]. The observed molecular conformation suggests a delocalization of pi-electrons extended over the diazoamine group and the terminal aryl substituents. Intermolecular N-H.O interactions between the twofold screw-related molecules give rise to helical chains along the [010] direction. Intermolecular C-H.O interactions then generate sheets of molecules in the (10-1) plane, and these sheets are held together by N.C and O.O pi-pi interactions.

1,3-Bis(2,4-dibromophenyl)triazene.

The crystal structure of the title compound, C(12)H(7)Br(4)N(3), shows that the stereochemistry about the N[double bond]N double bond of the N[double bond]N-N(H) moiety is trans. The whole molecule deviates slightly from planarity (r.m.s. deviation 0.164 A). While one of the aryl substituents is almost coplanar with the triazene chain, weak intermolecular Br...C contacts cause the second aryl substituent to deviate by an angle of 9.1 (8) from the plane defined by the N[double bond]N-N group. Weak intermolecular N-H...Br interactions between molecules related by the diagonal glide plane give rise to chains, which are stacked along the [100] crystallographic direction. An unequal distribution of double-bond character between the N atoms suggests a delocalization of pi electrons over the diazoamino group and the adjacent aryl groups.

cis-Bis­[1,3-bis(2-fluoro­phenyl)­triazenido-κ2N1,N3]­bis­(pyridine-κN)cadmium(II)

In the title compound, [Cd(C12H8F2N3)2(C5H5N)2], the Cd atom lies on a crystallographic twofold axis in space group Iba2. The coordination geometry about the Cd(II) ion corresponds to a rhombically distorted octahedron, with two deprotonated 1,3-bis(2-fluorophenyl)triazenide ions, viz. FC6H4NNNC6H4F-, acting as bidentate ligands (four-electron donors). Two neutral pyridine (py) molecules complete the coordination sphere in positions cis with respect to one another. The triazenide ligand is not planar (r.m.s. deviation = 0.204 A), the dihedral angle between the phenyl rings of the terminal 2-fluorophenyl substituents being 24.6 (1) degrees. The triazenide and pyridine Cd-N distances are 2.3757 (18)/2.3800 (19) and 2.3461 (19) A, respectively. Intermolecular C-H.F interactions generate sheets of molecules in the (010) plane.

3-(4-Acetylphenyl)-1-(4-nitrophenyl)triazene.

The crystal structure of the title compound, C(14)H(12)N(4)O(3), shows that the stereochemistry about the N=N double bond of the N=N-N(H) moiety is trans. The whole molecule is almost planar (r.m.s. deviation = 0.0654 A), the interplanar angle between the phenyl rings being 0.7 (1) degrees and the largest interplanar angle being that between the phenyl ring and the nitro group of the 4-nitrophenyl substituent [11.5 (2) degrees ]. Intermolecular N-H.O interactions between molecules related by translation give rise to chains along the [110] and [1-10] directions, and these chains are held together by N.O pi-pi interactions. An unequal distribution of the double-bond character among the N atoms suggests a delocalization of pi electrons over the diazoamine group and the adjacent aryl substituents.

1,2-Bis(2-tert-butylphenylimino)-1,2-dihydroacenaphthylene

The crystal structure of the title compound, C32H32N2, reveals a dimeric association of -diimine units into centrosymmetric dimers via intermolecular non-classical C—H N hydrogen bonds. There is also intramolecular non-classical C—H N bonding between the methyl groups and the N atoms of the diimine unit. In addition, the crystal packing indicates – interactions between acenaphthylene rings [3.888 (7) Å]. The deviation from a planar arrangement of the molecule can be attributed to both interand intramolecular non-classical hydrogen bonding.

Synthesis and Crystal Structure of [Bis(N-oxo-2-acetylpyridine 4N-Methylthiosemicarbazone)zinc(II)] Monohydrate

Abstract The reaction of zinc(II) acetate dihydrate and the tetra-dentate N-Oxo-2-acetylpyridine 4N-methylthiosemicarbazone (H4MLO) produces the novel complex [Zn(C9H11N4OS)2·H2O] (1). The complex crystallizesoin the orthorhombic space group Pbca with a = 15.871(3), b =16.890(3), c = 17.189(3) Å ,V - 4608(1) Å3, Z = 8 . The Zn(II) ion is tetra-coordinated via the thiolate sulfur atom and the azomethine nitrogen atom of two deprotonated ligands. In the solid state, 1 is polymerized via hydrogen bonds with a water molecule of crystallization.

Synthesis and Crystal Structure of a Novel Polymeric Lead(II) Complex with Thiosemicarbazonato and Thiocyanate Ligands

Abstract A novel heptacoordinated thiosemicarbazonato lead(II) complex [Pb(4ML)(SCN)] (4ML = 2-Acetylpyridine-4N-methylthiosemicarbazonato) was synthesized and characterized by conventional methods (IR and elemental analysis) and single-crystal X-ray diffraction. [Pb(4ML)(SCN)] shows an unusual polymeric structure in which the lead atom is hexa-coordinate, the deprotonated thiosemicarbazone both chelates and bridges, and the thiocyanate group acts as bridge between lead(II)-thiosemicarbazonate fragments. There is hydrogen-bonding between the polymeric chains. The complex crystallizes in the triclinic space group P 1̅̅ with a = 7.461(2), b = 9.572(2), c = 11.235(2) Å, α = 66.51(3), β = 84.01(3), γ = 68.75(3)°, V = 685.1(2) Å3, Z = 2.