2-Methyl­benzimidazolium thio­cyanate–2-methyl­benzimidazole (1/1)

In the crystal structure of the title compound, C8H9N2 +·SCN−·C8H8N2, the three components are linked by inter­molecular N—H⋯N and N—H⋯S hydrogen bonds into infinite chains along the c axis

2-Methyl­benzimidazolium thio­cyanate

In the crystal structure of the title compound, C8H9N2 +·SCN−, the nearly planar 2-methyl­benzimidazolium cation [r.m.s. deviation = 0.0123 (4) Å] is perpendicular to a mirror plane and the methyl H atoms are disordered about the mirror plane with equal occupancies. The thio­cyanate anion also lies on a mirror plane. N—H⋯N hydrogen bonds link the components into an infinite chain along the b axis

DNA Fingerprinting of the Local Pathogenic Bacteria Which Treated with Copper

Copper (Cu) is an essential trace element for all aerobic organisms. It functions as a cofactor in enzymes that catalyze a wide variety of redox reactions due to its ability to cycle between two oxidation states, Cu(I) and Cu(II). This same redox property of copper has the potential to cause toxicity if copper homeostasis is not maintained. Studies suggest that the toxic properties of copper are harnessed by the innate immune system of the host to kill bacteria. The aim of this research is show the DNA fingerprinting of two local pathogenic bacteria(Staphlococcus aureus isolated from body fluid and  E.coli isolated from urine) which treated with Copper  to clarify the role of copper's antibacterial activity against bacterial species could be utilized in health care facilities and in food processing plants. Keywords: Staphlococcus aureus, E.coli, Copper, copper's antibacterial

Synthesis and Study of Mixed Ligand-Metal Complexes of 1, 3, 7-Trimethylxanthine and 1, 3-Dimethyl-7H-purine-2, 6-dione with Some Other Ligands

This work presents synthesis and study of a new mixed ligand metal complexes of 1,3,7-trimethylxanthine and 1,3-dimethyl-7H-purine-2,6-dione with some other ligands like SCN and OCN ions to give the general formula [M(Tx)2(Tp) )2XY] where M=Co(II), Ni(II), Cu(II), Zn(II) and Cd(II), Tx=1,3,7-trimethylxanthine, Tp= 1,3-dimethyl-7H-purine-2,6-dione, X= SCN and Y= OCN. The resulting products were found to be solid which have been characterized using UV-Visible and infrared spectroscopy. Elemental analyses were performed using C, H, N analysis and atomic absorption techniques. The magnetic susceptibility and the conductivity were also measured. The present results suggest that the 1,3,7-trimethylxanthine and 1,3-dimethyl-7H-purine-2,6-dione were coordinated with metal ions through the nitrogen atom. Thiocyanate ion was coordinated with metal ions through the sulfur atom and the cyanate ion was coordinated with metal ions through the oxygen atom

Preparation and Spectral Properties of Mixed-Ligand Complexes of VO(IV), Ni(II), Zn(II), Pd(II), Cd(II) and Pb(II) with Dimethylglyoxime and N-Acetylglycine

Abstract: A number of mixed-ligand complexes of the general formula [M(D)(G)] where D=dimethylglyoximato monoanion, G=N-acetylglycinato and M=VO(IV), Ni(II), Zn(II), Pd(II), Cd(II) and Pb(II) were prepared. Each complex was characterized by elemental analysis, determination of metal, infrared spectra, electronic spectra, ( 1 H and 13 C) NMR spectra, conductivity and magnetic moments. All these complexes were not soluble in some of the organic solvent but highly soluble in dimethylformamide. The conductivity data showed the non-electrolytic nature of the complexes. The electronic spectra exhibited absorption bands in the visible region caused by the d-d electronic transition such as VO(IV), Ni(II) and Pd(II). The IR and ( 1 H, 13 C) NMR spectra which have indicate that the dimethylglyoxime was coordinated with the metal ions through the N and O atoms of the oxime group and Nacetylglycine was coordinated with metal ions through the N atom and terminal carboxyl oxygen atom

Preparation and Spectral Properties of Mixed-Ligand Complexes of VO(IV), Ni(II), Zn(II), Pd(II), Cd(II) and Pb(II) with Dimethylglyoxime and N-acetylglycine

A number of mixed-ligand complexes of the general formula [M(D)(G)] where D=dimethylglyoximato monoanion, G=N-acetylglycinato and M=VO(IV), Ni(II), Zn(II), Pd(II), Cd(II) and Pb(II) were prepared. Each complex was characterized by elemental analysis, determination of metal, infrared spectra, electronic spectra, (1H and 13C) NMR spectra, conductivity and magnetic moments. All these complexes were not soluble in some of the organic solvent but highly soluble in dimethylformamide. The conductivity data showed the non-electrolytic nature of the complexes. The electronic spectra exhibited absorption bands in the visible region caused by the d-d electronic transition such as VO(IV), Ni(II) and Pd(II). The IR and (1H, 13C) NMR spectra which have indicate that the dimethylglyoxime was coordinated with the metal ions through the N and O atoms of the oxime group and N-acetylglycine was coordinated with metal ions through the N atom and terminal carboxyl oxygen atom

Preparation and study of some Mn(II), Co(II), Ni(II), Cu(II), Cd(II) and Pb(II) complexes containing heterocyclic nitrogen donor ligands, E-Journal of Chemistry

Abstract: This paper presents a new mixed-ligand complexes with the general formula [M(BT)(BI) 2 X 2 ] where BT=benzotriazole, BI=benzimidazole, X=SCN and M=Mn(II), Co(II), Ni(II), Cu(II), Cd(II) and Pb(II). The reaction was carried out by using the appropriate molar ratios of metal:ligand (1:1:2:2) (M:BT:BI:X) as required. The resulting products were found to be solids, not soluble in water and in ordinary organic solvents but highly soluble in DMSO. These complexes have been studied by UV-Visible, IR and ( 1 H, 13 C) NMR spectra, molar conductivity, elemental analysis of C, H, N, determination of metal and magnetic susceptibility. The result suggests that the benzimidazoleas as a monodentate was coordinated with the metal ions through the N atom. Nevertheless, the benzotriazole as bidentate was coordinated with the metal ions through the N2 and N3 atoms. SCN was coordinated with the metal ions through the nitogen atom

Synthesis, Spectral and Magnetic Studies of Newly Mixed-Ligand Complexes of 4-Formyl-Acetanilide Thiosemicarbazone and 3,4-Dihydrocinnamic Acid with Some Metal Ions

New complexes with thiosemicarbazone derivative and 3, 4-dihydrocinnamic acid were prepared and characterized by elemental analysis, determination of metal, IR, 1H NMR, electronic spectroscopy and magnetic measurements. The thiosemicarbazone derivative forms bidentate ligand complexes of the general formula, [M(Thz)(Caf)] where Thz = 4-formyl- acetanilide thiosemicarbazone, Caf = 3,4-dihydrocinnamic acid and M=Mn2+, Fe2+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+ and Pb2+. The IR and 1H NMR spectra indicates that the (Thz) was coordinated with the metal ions through the N and S atoms and the (Caf) was negatively charged bidentat ligand and was coordinated with the metal ions through the two O atoms. Electronic spectra and magnetic susceptibility measurements of the solid complexes indicates the tetrahedral geometry around the Mn2+, Fe2+, Co2+, Ni2+, Zn2+, Cd2+ and irregular tetrahedral geometry around Pb2+ ion while the Cu2+ complex has squar planer geometry

Synthesis and characterization of mixed ligand complexes of caffeine, adenine and thiocyanate with some transition metal ions

An ethanolic solution of caffeine was added to an aqueous solution of metal salts and followed by adding ethanolic solution of adenine and an aqueous solution of potassium thiocyanate to give complexes with general formula [M(CA)2(Ad)X2] where CA is caffeine, Ad is adenine, X is thiocyanate ion and M is Co(II), Ni(II), Cu(II), Zn(II) and Cd(II). The resulting products were characterized using UV-visible and infrared spectroscopies. Elemental analyses were performed using C, H, N analysis and atomic absorption techniques. The magnetic susceptibility and the conductivity were also measured. The results suggested that the complexes have octahedral geometry

Di-μ-thiocyanato-κ2N:S;κ2S:N-bis[bis(2-methyl-1H-benzimidazole-κN3)(thiocyanato-κN)cadmium(II)]

The title compound, [Cd2(NCS)4(C8H8N2)4], is a centrosymmetric dinuclear cadmium(II) complex in which each two metal ions are linked by a pair of thiocyanate N:S-bridges. Two 2-methylbenzimidazole N-atom donors and one terminal thiocyanate N atom complete a highly distorted square-pyramidal geometry around the Cd atom. In the crystal structure, two N—H...S hydrogen-bonding interactions occur, resulting in a three-dimensional polymeric structure. The apical 2-methylbenzimidazole ring and its symmetry-related counterpart are arranged in an antiparallel manner with a centroid–centroid separation of 3.6050 (14) Å, indicative of a π–π interaction