Antitumor Metallothiosemicarbazonate： Synthesis,Crystal Structure,Spectra and Antitumor Studies of Co（Ⅲ） Complex with Thiosemicarbazone Derivative of 2-Benzoylpyridine

The title complex [Co（L）2]Cl·4H2O I has been achieved via self-assembly by incorporating cobalt into 2-benzoylpyridine thiosemicarbazonate ligand, and characterized by elemental analysis, infrared spectra, mass spectra and single-crystal X-ray diffraction study. The crystal crystallizes in monoclinic, space group P2 1/n, with a = 10.227（3）, b = 17.363（4）, c = 17.459（4） A, β= 100.408（4）°, V= 3049.2（13） A^3, Z = 4, Mr = 677.08, Dc = 1.475 g/cm^3, μ（MoKα） = 0.834 mm^-1, F（000） = 1400, the final R = 0.0747 and wR = 0.0896 for 1663 observed reflections with I 〉 2σ（I）. The complex contains one six-coordinated cobalt ion connected by two thiosemicarbazone ligands which act as a tridentate ligand to coordinate with the center metal atoms via two pyridyl nitrogen atoms, two imine nitrogen atoms and two sulfur atoms giving rise to a mononuclear structure. Hydrogen bonds existing in the complex link the different components to stabilize the crystal structure. The antiturnor activity of the title complex was tested against A549 lung cancer cell line. Complex ! exhibits antitumor activity.     

Synthesis and Crystal Structure of a Mn(Ⅱ) Complex with Thiosemicarbazone Derivative of Pyridine-3-carbaldehyde Showing Unusual Coordination Mode of Tridentate Thiosemicarbazone

The title complex Mn(HL)4(NCS)2(CH3CH2OH)2 has been achieved via selfassembly by incorporating manganese(Ⅱ) into pyridine-3-carbaldehyde thiosemicarbazonate ligand,and characterized by elemental analysis and single-crystal X-ray diffraction study. The crystal crystallizes in triclinic, space group P1 with a = 8.896(2), b = 9.530(2), c = 14.520(4) (A), α =87.035(4), β= 88.112(4), γ= 69.434(4)°, V= 1150.9(5) (A)3, Z = 1, Mr = 984.17, Dc = 1.420 g/cm3,μ(MoKα) = 0.612 mm-1, F(000) = 511, the final R = 0.0574 and wR = 0.1547 for 2855 observed reflections with I ＞ 2σ(I). The complex contains one six-coordinated manganese ion connected by two thiosemicarbazide ligands, in which the thiosemicarbazone ligand acts as a monodentate ligand and coordinates to the center metal atoms via the pyridyl nitrogen atoms, two ethanol molecules and two isothiocyanic anions to give rise to a mononuclear structure. The coordination of a potentially tridentate thiosemicarbazone in manganese(Ⅱ) complex without using its sulfur and imine nitrogen sites is unusual. Hydrogen bonds existing in the complex link the different components to stabilize the crystal structure.     

Synthesis and Crystal Structure of a Mn(II) Complex with Thiosemicarbazone Derivative of Pyridine-3-carbaldehyde Showing Unusual Coordination Mode of Tridentate Thiosemicarbazone

1 INTRODUCTION Heterocyclic thiosemicarbazones as well as their metal complexes have been attracting considerable interest due to their biological activities, such as antiviral, antibacterial, antimalarial, antifungal, and antitumoral activities[1～5]. This prompted us to carry out structural studies of these complexes to provide a basis for understanding their behaviors in living systems. Although quite a number of investigations on the 2-heterocyclic thiosemicarbazones have ap- peared[6…     

Synthesis, Crystal Structure, and Spectral Properties of a Novel Co(Ⅱ) Complex Containing Imidazole Derivative

A novel imidazole derivative with functional group and π-conjugated system, 1- [trans-4-(4-diethylaminostyryl)phenyl]imidazole (abbreviated as L), and its CoII complex (CoCl2L4)2 (Co2C168H184N24Cl4, Mr = 2799.05 ) have been synthesized and the crystal structure of the latter was determined by X-ray diffraction. The crystal is of triclinic, space group P with a = 8.823(3), b = 18.799(7), c = 23.065(9) (A), α = 77.349(6), β = 83.128(7), γ = 80.942(3)°,V = 3671.5(12)(A)3, Z = 1, Dc = 1.266 g/cm3, μ = 0.361 mm-1, F(000) = 1482, the final R = 0.0587 and Wr = 0.1284 for 6562 observed reflections with Ⅰ ＞ 2б(Ⅰ). In the molecular structure of (CoCl2L4)2, there are two crystallographically unique units. The CoII atoms are six-coordinated by four N atoms from four imidazole ligands (L) and two Cl atoms to form a distorted octahedral geometry. The optical properties of complex (CoCl2L4)2 have been experimentally studied.     

Synthesis,Crystal Structure,and Spectral Properties of a Novel Co(II) Complex Containing Imidazole Derivative

1 INTRODUCTION The metal-organic frameworks constructed from metals and π-conjugated ligands might have poten- tial applications in various fields, such as electronic, optical or magnetic materials[1～3]. Therefore, this kind of complex has attracted the increasing atten- tion of chemists, and considerable efforts have been devoted to the rational design and synthesis of new materials[4, 5]. Moreover, the organic-inorganic hybri- dized coordination complexes with imidazole deri- vatives …     

Synthesis, Crystal Structure and DNA-binding Property of Bismuth(Ⅲ) Complex with p-Hydroxy-phenylacetic Acid

A bismuth(Ⅲ) complex 1 (H2-4,4'-bipy)Bi(HPPA)5(H2PPA)·4H2O (H2PPA = p-hydroxy-phenylacetic acid, 4,4'-bipy = 4,4 -bipyridyl) was hydrothermally synthesized from p-hydroxy-phenylacetic acid (H 2 PPA), Bi(NO 3) 3 ·6H 2 O and 4,4 -bipyridyl, and characterized by elemental analysis, IR, molar conductivity and TG. The single-crystal X-ray diffraction studies demonstrated that the complex is of monoclinic system, space group P21 with a = 10.928(7), b = 22.558(7), c = 11.313(7), β = 91.864(4)°, V = 2787.7(4)3 , Z = 2, C58H61BiN2O22 , Mr = 1347.07, F(000) = 1364, Dc = 1.605 g/cm-3 , μ(MoKα) = 3.247 mm-1 , the final R = 0.0269 and wR = 0.0540 for 9776 observed reflections with Ⅰ > 2σ(Ⅰ). The bismuth(Ⅲ) is seven-coordinated with O atoms, forming a monocapped octahedral geometry. Complex 1 further forms a 3D supramolecular architecture by hydrogen bonds and π-π stacking interactions. Moreover, the interaction between the complex and DNA was studied by EtBr fluoescent probe.     

Synthesis and Crystal Structure of Cobalt(Ⅲ) Tris(diethyldithiocarbamato) Complex

1INTR0DUCTI0NRecently,thedesignandsynthesisofdinuclearcomplexeshavebeenafascinat-ingareaofresearchowingt0theirimportanceinbasicandappliedchemistry"'.Par-ticularintersthasdevelopedindinuclearcomplexesasmodelsformeta1loproteins"'.Inanattempttosynthesizethetypeof[Ln(S,CN(C2H,)2)3j[Co(S2CN(C2H5)2)2jdinuc1earcomplex,thepurefinecrystalsofCo[S2CN(C2H5)2)2)3were0btained.2EXPERIMENTAL2'1Preparation0fC0[S,CN(C,H,),j,TotheclearsolutionoftheanhydrousSmCl3(0.5mmol)in5mLanhydrousethanolw…     

Synthesis and Crystal Structure of Copper(Ⅱ)Complex with N-Acetoxyl-picolinamide

Using Cu(Ⅱ) as the template, a complex {[Cu2L2(H2O)2] 4H2O}n (L = N-acetoxyl- picolinamide) has been successfully synthesized and characterized by single-crystal X-ray diffrac tion. The crystal is of monoclinic, space group C2/c, with a = 24.144(5), b = 7.1622(14), c = 17.283(4) (A), C16H24Cu2N4O12, Mr = 591.47, β = 131.73(3)°, V = 2230.3(8) (A)3, Z = 4, Dc= 1.761 g/cm3, F(000) = 1208,μ = 1.978 mm-1, R = 0.0400 and wR = 0.1099. The copper (Ⅱ) ion is five coordinated with a distorted square pyramidal geometry. The complex can be viewed as a one dimensional chain structure by carboxylic bridges among copper atoms. In the complex there exist hydrogen bonding interactions to stabilize the structure.     

Synthesis and Crystal Structure of Copper(II) Complex with N-Acetoxyl-picolinamide

1 INTRODUCTION The picoloylhydrazide compounds are close to thebiologic environment and can react with microele-ments in organism so as to have antitubercular andantineoplastic activities. However, owing to the exis-tence of amino group, this kind of compounds aretoxic to some extent[1]. In order to decrease theirtoxicity, hydrazone or hydrazide compounds synthe-sized by the condensation reaction of amino and car-bonyl groups have been well studied in recentyears[1～7]. Herein we report t…     

Synthesis and Crystal Structure of Zn(Ⅱ) Complex with 2-Aminopyridine and Acetylacetone

A mixed complex [Zn(C5H6N2)(HL)2] (C5H6N2 = 2-aminopyridine, H2L = acetyl- acetone) has been synthesized and characterized by IR, elemental analysis and X-ray single-crystal diffraction analysis. The crystal belongs to monoclinic, space group P21/c with a = 7.4490(15), b = 8.2650(17), c = 27.615(6)(A),β = 101.69(3)°, V = 1664.9(6)(A)3, Z = 4, Mr = 357.70, Dc = 1.427 g/cm3, F(000) = 744, μ = 1.493 mm-1, R = 0.0309 and wR = 0.0771. The Zn(II) is coordinated by one nitrogen atom from 2-aminopyridine and four oxygen atoms from two acetylacetone anions to furnish a distorted square pyramid geometry. The complex forms a three-dimensional network through intermolecular hydrogen bonds.     

Synthesis,Crystal Structure and Antitumor Activity of a Novel Zn(Ⅱ) Complex with 2-(Nicotinoyloxy)acetic Acid Ligand

A novel Zn(Ⅱ) complex, [ZnL_2(H_2O)_4]·H_2O(1, HL = 2-(nicotinoyloxy)acetic acid), was synthesized using Zn(OAc)_2·2H_2O and 2-(nicotinoyloxy)acetic acid as raw materials. Its structure has been elucidated by elemental analysis, IR and single-crystal X-ray diffraction. The structural analysis revealed that complex 1 crystallizes in triclinic, space group P1 and the Zn(Ⅱ) atom is six-coordinated with two N atoms from two different 2-(nicotinoyloxy)acetate anion ligands and four O atoms from coordinated water molecules. Complex 1 forms a 3D network structure by O–H···O hydrogen bonds. The antitumor activities of 2-(nicotinoyloxy)acetic acid ligand and its Zn(Ⅱ) complex were evaluated against human lung adenocarcinoma A549 cells, human hepatoma SMMC-7721 cells and human colon carcinoma Wi Dr cells.     

Synthesis and Crystal Structure of Ni(Ⅱ) Complex with N-Salicylaldehyde-N''''-phenoxyacetylhydrazine Ligand

1INTRODUCTIONHydrazoneshavebeenattractingmuchatten-tionfromchemistsinrecentyearsbecauseoftheirbiologicalactivities,chemicalandindustrialversa-tility,andstrongtendencytochelatetotransitionmetals[1,2],lanthanidemetals[3]andmaingroupmetals[4,5].Inthehydrazonecomplexes,thehydra-zoneligandcanactasaneutralormononegativebidentateligand,orevenasadianionictridentateliganddependingonthedonoratomsoftheligandsandthereactionconditions.Ontheotherhand,variouscompoundsderivedfromphenoxyaceticacidareveryus…     

Synthesis,Crystal Structure,and Studies on Mechanism of D-π-A Ferrocene Derivative

Russian Journal of Coordination Chemistry - Microwave-assisted solvent-free synthesis of new (D-π-A) chromogenes, 2-ferrocenyl-1,1-dicyanobuta-1,3-diene derivatives (II), have been...     

Synthesis, Characterization and Crystal Structure of Chlorodibenzyltin(IV) Complex with Dithiomorpholinocarba-mate Ligand

ＩｎｔｒｏｄｕｃｔｉｏｎＯｒｇａｎｏｔｉｎ(ＩＶ)ｃｏｍｐｌｅｘｅｓｗｅｒｅｗｉｄｅｌｙｕｓｅｄａｓｂｉｏ ｃｉｄｅｓ,ｆｕｎｇｉｃｉｄｅｓａｎｄｉｎｉｎｄｕｓｔｒｙａｓｈｏｍｏｇｅｎｅｏｕｓｃａｔａ ｌｙｓｔｓ.1 6 Ｍｏｒｅｒｅｃｅｎｔｌｙ ,ｐｈａｒｍａｃｅｕｔｉｃａｌｐｒｏｐｅｒｔｉｅｓｏｆａｌｋｙｌｔｉｎ(ＩＶ)ｃｏｍｐｌｅｘｅｓｗｉｔｈＮ ,Ｎ ｄｉａｌｋｙｌｄｉｔｈｉｏｃａｒｂａ ｍａｔｅｌｉｇａｎｄｓｈａｖｅｂｅｅｎｉｎｖｅｓｔｉｇａｔｅｄｆｏｒｔｈｅｉｒａｎｔｉｔｕｍｏｕｒａｃｔｉｖｉｔｙ.7,8…     

Synthesis and Crystal Structure of a Chiral Manganese(Ⅲ) Schiff Base Complex

A chiral salency complex,[Mn(Salency)(H2O)2](PF6)·2H2O 1(Salency =(R,R)-N,N'-bis(salicylidene)-1,2-cyclohexanediamine),has been prepared by the reaction of Mn(CH3COO)3·2H2O with Salency and NH4PF6,and was established by X-ray diffraction techniques.The complex crystallizes in triclinic,space group P1 with a=9.299(8),b=10.012(8),c=13.461(11),α=92.037(15),β=92.974(12),γ=93.530(18)°,V=1248.3(18)3,C20H28F6MnN2O6P,Mr = 592.35,Z=2,Dc=1.038 g/cm3,F(000)=608,μ=0.676 mm-1,the final R=0.0651 and wR=0.1880 for 5260 observed reflections with I 2σ(I).     

Synthesis and Crystal Structure of a New Lanthanum(Ⅲ) 4-Cyanobenzoate Complex

A new dinuclear La(Ⅲ) complex [La2(4-cba)4[H(4-cba)2]2(phen)2(H2O)4] (4-Hcba = 4-cyanobenzoic acid and phen = 1,10-phenanthroline) 1 has been synthesized by solvothermal reaction in an ethanol/water mixed solution at 100 ℃ and structurally characterized by single- crystal X-ray diffraction. Crystallographic data: C88H58La2N12O20, Mr = 1881.28, triclinic P(1), a = 7.518(3), b = 17.033(6), c = 17.551(6)(A), α = 115.333(4), β = 92.9910(10), γ = 99.366(5)°, V = 1985.3(12) (A)3, Z = 1, Dc = 1.574 g/cm3, F(000) = 944 μ = 1.145 mm-1, the final R = 0.0281 and wR = 0.0686 for 6708 reflections with Ⅰ ＞2σ(Ⅰ). In 1, two nine-coordinated La(Ⅲ) ions are connected by two 4-cba ligands in a syn-syn bidentate coordination mode, and the other six 4-cba ligands terminate the La(Ⅲ) ions, resulting in an isolated dinuclear structure. Two different types of intramolecular hydrogen bonds, asymmetrical O-H…O and symmetrical O…H…O, exist in the crystal. The title complex molecules are connected through hydrogen bonds and weak π-πstacking interactions to generate a 2-D layered network. The thermogravimetric analysis of 1 has also been discussed.     

Synthesis and Crystal Structure of a Novel Fe(Ⅲ) Schiff Base Complex

A novel Fe(Ⅲ) Schiff base complex,FeⅢ(HL) {H4L = 1,1,1,1-tetrakis[(salicylaldimino)methyl]methane},has been prepared and characterized by elemental analyses,IR spectrum,and single-crystal X-ray diffraction analysis.The crystal belongs to the monoclinic system,space group P21/n with a = 12.569(3),b = 12.955(3),c = 17.647(4) ,β = 91.896(9)°,V = 2871.9(1) 3,Z = 4,Dc = 1.391 g/cm3,F(000) = 1252.0,Mr = 601.45,R = 0.0383 and wR = 0.1025.The structural analysis reveals that the Fe(Ⅲ) ions are six-coordinated by imine nitrogen atoms and phenolic oxygen atoms form three pendant arms of Schiff base ligands,and one of the salicylaldimine chelating units remains uncoordinated.Discrete complex molecules were further assembled into 1D supramolecular aggregations by C-H…O hydrogen bonding and C-H…π interactions.     

Synthesis,Crystal Structure and in vitro Anticancer Studies of 1,2-Bis-benzimidazole-phenyl Copper(Ⅱ) Complex

One new benzimidazole derivative copper(II) complex 1(C10H6Cu N2, Mr = 217.71) has been synthesized and characterized by FT-IR and X-ray single-crystal diffraction. It crystallizes in orthorhombic, space group Pbcn with a = 17.417(2), b = 8.9963(8), c = 11.3432(9) ?, V = 1777.3(3) ?3, Z = 8, μ(Mo Kα) = 2.403, F(000) = 872, Dc = 1.627 g/cm3. The final R = 0.0598 for 1153 observed reflections with I 2σ(I) and w R = 0.17 for all data. The in vitro anti-cancer activities of 1, Cu Cl2 and the benzimidazole ligand L were investigated using human cervical(Hela) and hepatocellular carcinoma(Hep-G2) cancer cell lines. The copper(II) complex can greatly inhibit the cell proliferation and show stronger cytotoxic activities against the tested cancer cell lines than both the ligand and copper(II) salt.