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.     

K_(10)[H_2W_(12)O_(42)]·11H_2O的合成及晶体结构分析

在水溶液中反应制得无色透明的标题化合物单晶 ,单晶X -射线结构分析表明 ,属单斜晶系 ,空间群P2 1,晶胞参数 :a=1.15 47(2 )nm ,b =1.430 9(3)nm ,c =1.5 495 (3)nm ,β =10 5 .41(3)° ,V =2 .46 81(9)nm3,Z =2 ,Dc=4.6 39Mg/m3,对 5 45 4个独立衍射点 (I>2δ(I) )进行全矩阵最小二乘法修正后 ,可靠性因子R =0 .0 487     

Hydrothermal Synthesis and Structure Characterization of a Novel 4,4′-Bipyridine Bridging Dumbbell-like Dimeric Pentamolybdate

1 INTRODUCTION Polyoxometalates (POMs) have been attracting extensive interest of many chemists in solid-state materials chemistry owning to the various structures and great potential applications in catalysis, medi- cine, photo-electricity and magnetism[1～9]. Over the past decades, lots of novel POMs have been pre- pared by hydrothermal synthesis, such as discrete structure[10], one-dimensional chain-like structure[11, 12] and higher dimensional architecture[13～18]. However, in these…     

超分子化合物[C6H11NH3]6[P2Mo18O62]·4H2O的水热法合成及结构

超分子化合物[C6H11NH3]6[P2Mo18O62]·4H2O的水热法合成及结构;Wells-Dawson结构;杂多化合物     

多钼酸盐[4,4''-H2 bipy]2[β-Mo8O26]的水热合成和晶体结构

利用水热合成方法制备了化合物[4,4'-H2bipy]2[β-Mo8O26],用元素分析、X射线单晶衍射和电子顺磁共振对其结构进行了表征.结构解析表明标题化合物是由β型[Mo8O26]4-多阴离子与质子化的4,4'-联吡啶通过氢键作用形成的三维结构超分子化合物.     

多钼酸盐[4,4-′H_2bipy]_2 [β-Mo_8O_(26)]的水热合成和晶体结构

利用水热合成方法制备了化合物[4,4′-H2b ipy]2[-βMo8O26],用元素分析、X射线单晶衍射和电子顺磁共振对其结构进行了表征.结构解析表明标题化合物是由β型[Mo8O26]4-多阴离子与质子化的4,4′-联吡啶通过氢键作用形成的三维结构超分子化合物.     

一维锯齿状化合物[(en)_2(Mo_6O_(20)H_4)]_n的水热合成及晶体结构

利用Na2MoO4·2H2O,MoO3,乙二胺,和H2O通过水热合成法合成了一维锯齿状化合物[(en)2(Mo6O20H4)]n.晶体解析表明,该化合物属于单斜晶系,P21/n空间群,a=0.80680(16)nm,b=1.4371(3)nm,c=0.88874(18)nm,β=97.89(3)°,V=1.0207(4)nm3,Z=2,Dc=3.305Mg·m-3,μ=3.681mm-1,F(000)=960.该化合物结构单元由二个游离的乙二胺分子和一个阴离子Mo6O4-20阴离子中,六20构成.在Mo6O4-个钼原子和八个相邻的氧原子构成两个八员环,在每个八员环的两侧分别存在着一个与三个钼原子相连的桥氧.     

多钼酸盐[4，4′-H2bipy]2[β-Mo8O26]的水热合成和晶体结构

利用水热合成方法制备了化合物[4，4′-H2bipy]2[β-Mo8O26]，用元素分析、X射线单晶衍射和电子顺磁共振对其结构进行了表征．结构解析表明标题化合物是由／3型[Mo8O26]^4-多阴离子与质子化的4，4’-联吡啶通过氢键作用形成的三维结构超分子化合物．     

Synthesis and Structure of a Novel 3-Fold Interpenetrating Three-dimensional Coordination Polymer：[Ni（Hbyip~（2-））（bix）_（0.5）（H_2O）]_n

A three-dimensional coordination polymer,[Ni(Hbyip2-)(bix)0.5(H2O)]n,has been hydrothermally synthesized.Each Ni2+ ion is five-coordinated by three carboxylate O atoms from three different 5-(benzoic acid-4-yldiazenyl)isophthalate(Hbyip2-) anions,one N atom from one 1,4-bis(imidazol-1-ylmethyl)benzene(bix) ligand and one O atom from an aqua ligand displaying a distorted square-pyramid.Each Ni atom is defined by three Hbyip2-anions and each Hbyip2-anion adopts a tris(mono-dentate) ligand coordinating to three Ni2+ ions affording a 36-membered inorganic ring.These rings are further arranged into an undulated two-dimensional layer parallel to the(101) plane.Adjacent two-dimensional networks are linked by bix ligands into a three-dimensional {63,83}{63} framework with a large channel(ca.26.3 × 13.6) along the [100] direction.Each individual {63,83}{63} network interpenetrates with two others in a parallel fashion to generate a 3-fold interpenetrating network.     

Synthesis and Crystal Structure of a Novel 2-Fold Interpenetrating Three-dimensional Coordination Polymer,{[Co_3（byip）_2（bix）_3（H_2O）_2]·H_2O}_n

The title coordination polymer including two crystallographically independent Co2+ ions is hydrothermally synthesized, in which the Co(1) 2+ ion is four-coordinated by two carboxylate oxygen atoms from two different 5-(benzoic acid-4-yldiazenyl)isophthalate (byip3-) anions and two nitrogen atoms from two distinct 1,4-bis(imidazol-1-ylmethyl) benzene (bix) ligands displaying a tetrahedral geometry. The Co(2) 2+ ion is six-coordinated by two water molecules at the apical positions, and two carboxylate oxygen atoms and two nitrogen atoms at the equatorial positions, affording a slightly distorted octahedron. Two Co(1)2+ and two Co(2)2+ ions are linked together by four byip3- anions forming a 44-membered motif and these motifs are further arranged into a three-dimensional framework through bix ligands along the a axis with a larger channel (ca. 22.70×11.01). Each individual network interpenetrates with the other identical network in a parallel fashion to generate a 2-fold interpenetrating array with the {62.84}{63}2{64.82}2 topology.