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CRYSTAL STRUCTURE OF [Ni((C6H11O)2PS2).(C4H9NH2)3]—(C6H11O)2PS2 总被引:5,自引:1,他引:5
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用光谱法研究了Ni[(C_6H_(11)O)_2PS_2]_2与吡啶的加合反应,测定了平衡常数,用单晶X射线衍射方法测定了的晶体结构.晶体空间群P_T,晶胞参数为. 相似文献
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二烃基二硫代磷酸酯及其过渡金属配合物能阻止烃类自动氧化 ,是一种很重要的抗氧剂、抗磨剂。也被广泛用作石油的添加剂 ,高分子材料的稳定剂和人造橡胶的硫化促进剂[1~ 4 ] 。近年来的研究发现 ,该类配合物与胺类物质形成稳定的 1∶1五配位或 1∶2六配位加合物时 ,将改变原有配合物的特性 ,并能更有效地抑制氧化作用[5] 。本文合成了Ni[(C4 H9O) 2 PS2 ]2 ,考察其与乙胺、二乙胺和三乙胺的加合反应 ,测定了反应的平衡常数、热力学参数和加合物的组成比。1 实验部分无水乙醇、乙胺、二乙胺、三乙胺为A R级或C P级 ,使用前按文… 相似文献
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合成了一个新的三维超分子化合物[Ni(DMF)6]2[SiMo12O40]·H2O,通过红外光谱、X射线单晶衍射和热重分析等手段对其结构进行了表征.单晶结构解析结果表明,标题化合物属于三方晶系,船空间群,晶胞参数为:a=1.5902(4)nm,b=1.5902(4)nm,c=3.2281(17)nm,V=7.069(4)nm^3,Z=3,Dc=1.994g/cm^3,μ=2.032mm^-1.F(000):4146,R1=0.0516,ωR2=0.1453.配合物中镍离子采用6配位的八面体配位构型,晶体堆积中通过多种分子间氢键作用形成三维网状结构. 相似文献
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Katsuyuki Aoki 《高等学校化学研究》2005,21(4):396-400
Fe(Ⅱ) complex Fe[HB(pz)3]2(compound 1, pz=pyrazole) and Ni(Ⅱ) complex Ni[HB(pz)3]2(compound 2) have been obtained by the reaction of MCI2(M=Fe and Ni) with NaHB(pz)3 in MeOH. The two complexes(compounds 1 and 2) were characterized by IR, NMR, elemental analysis and X-ray diffraction. Compound 1 crystallizes in space group P21/c with a=1.224(3) nm, b=1.161(2) nm, c=1.648(3) nm, β=107.62(15)°, V=2.233(8) nm3, Z=2. Compound 2 crystallizes in space group P21/c with a=0.97926(18) nm, b=1.7423(3) nm, c=1.3156(2) nm, β=97.055(16)°, V=2.2277(7) nm3, Z=4. The results of X-ray structural analyses show that both compounds 1 and 2 are monomeric neutral, possessing a similar coordination mode and a similar structure around the metal centers. The related spectral characterizations, steric effects and binding properties are discussed. 相似文献
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LIAN Zhao-Xun ;LIU Ping ;ZHANG Jia-Min ;LOU Tian-Jun ;WANG Tian-Xi ;LI Hao-Hong 《结构化学》2008,27(6):639-644
The title compounds, Cu(L1)(C4H8NHO) and Ni(L2)(C4H8NHO) (H2L1 = 5-bromosalicylaldehyde-p-nitrobenzoylhydrazone, H2L2 = 5-bromosalicylaldehyde-p-hydroxybenzoylhydrazone), have been obtained and characterized by single-crystal X-ray diffraction. Complex 1 belongs to the triclinic system, space group P1 with a = 8.6960(2), b = 9.957(2), c = 11.878(2)A, α = 73.36(3), β = 78.25(3), γ = 82.64(3)°, V = 962.1(3) A^3, Mr= 512.81, Z = 2, F(000) = 514, Dc = 1.770 g/cm^3,μ(MoKα) = 3.251, R = 0.0337 and wR = 0.0846. Complex 2 is of monoclinic, space group P21/c with a = 13.313(2), b = 8.2096(1), c = 21.890(3) A,β = 125.737(3)°, V = 1941.9(4) A^3, Mr= 478.97, Z = 4, F(000) = 968, Dc = 1.638 g/cm^3,μ(MoKα) = 3.085, R = 0.0356 and wR = 0.0817. The ligands form a satisfactory N2O2 square plane around the metal centers in two compounds. Different patterns of hydrogen bonds are observed owing to the presence of different substituents on aromatic ring of the acylhydrazone Schiff bases. In complex 1, square-planar copper(Ⅱ) complexes are linked by intermolecular hydrogen bonds leading to zigzag infinite chains. In complex 2, the metal complexes are linked via hydrogen bonds to form corrugated sheets in a staggered fashion; 3D channels along the b axis are constructed through other non-covalent interactions between the neighboring layers. 相似文献
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合成了一个新的三维超分子化合物[Ni(DMF)6]2[SiMo12O40]·H2O,通过红外光谱、X射线单晶衍射和热重分析等手段对其结构进行了表征.单晶结构解析结果表明,标题化合物属于三方晶系,船空间群,晶胞参数为:a=1.5902(4)nm,b=1.5902(4)nm,c=3.2281(17)nm,V=7.069(4)nm^3,Z=3,Dc=1.994g/cm^3,μ=2.032mm^-1.F(000):4146,R1=0.0516,ωR2=0.1453.配合物中镍离子采用6配位的八面体配位构型,晶体堆积中通过多种分子间氢键作用形成三维网状结构. 相似文献
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Co[(C6H11O)2PS2]2·2Py的合成和晶体结构 总被引:2,自引:0,他引:2
Oxidation process of Co[(C6H11O)2PS2]2 and substitute-reduction reaction of Co[(C6H11O)2PS2]3 with pyridine have been studied by spectrophotometric methods, respectively. The equilibrium constant was found to be K=0.63±0.02(mol·dm-3)-3. The crystal structure of Co[(C6H11O)2PS2]2·2Py has been determined by X-ray diff- raction method. The crystal belongs to triclinic system, space group P1, with cell parameters: a=6.944(2)?,b=9.277(3)?,c=15.981(6)?,α=91.79(3)°,β=99.55(3)°,γ=94.44(3)°,V=1011.2(6)?3,Z=2,Mr=803.94,Dc=1.320Mg·m-3,F(000)=425,μ=0.747mm-1,final R=0.0700 and wR=0.1988 for 3626 re-flections with I≥2σ(I). The cobalt atom in the title complex has a octahedral geometry with four Co-S bonds and two Co-N bonds. The central atom P is tetrahedrally surrounded by two sulphur atoms and two oxygen atoms in the dicyclohexyldithiophosphate ligand. The six carbon atoms of cyclohexyl take the chair conformation. 相似文献
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Ni[S_2P(OCH_2CH_2Ph)_2]_2与4-甲基吡啶加合反应及加合物的结构表征 总被引:2,自引:0,他引:2
采用紫外光谱法研究了Ni[S_2P(OCH_2CH_2Ph)_2]_2与4-甲基吡啶的加合反应,测定了反应的平衡常数:β_1=39.5(R_1=1)和β_2=2.20×10_4(R_2=0.9981).用元素分析、红外光谱、单晶X-射线衍射法对合成的加合物Ni[S_2P(OCH_2CH_2Ph)_2]_2·(4-MePy)_2进行了结构表征.加合物为单斜晶系,空间群P2_1/c,晶胞参数:a=1.2920(4)mn,b=1.7498(4)nm,c=1.0979(3)nm,α=90.00°,β=113.05(3)β,γ=90.00°. 相似文献
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1 INTRODUCTIONRareEarth (RE)elementsareappliedinagricultureandmedicine .Therfore,betterunderstandingofthebondingofREionsinthecomplexeswithaminoacidsisnecessary .ThecrystalstructureofREcomplexeswiththesimplestaminoacidglycinewerestudiedbefore[1- 4].Toresearch… 相似文献
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以牛磺酸、邻香草醛为原料,合成了配体牛磺酸缩邻香草醛席夫碱,再用所得配体与醋酸镍、邻菲啰啉作用,合成了配合物[Ni(phen)2(tovsb)]·4H2O(phen=邻菲啰啉,tovsb=牛磺酸缩邻香草醛席夫碱),其结构通过IR,元素分析和x-射线单晶衍射法测定。标题配合物属三斜晶系,PI空间群;α=1.04661(16),b=1.2303(2),c=1.4063(2)nm,α=83.714(4),β=88.539(3),γ=69.398(3)°,V=1.6947(5)nm^3,Z=2。结构分析表明,两个邻菲哕啉共提供四个配位原子,牛磺酸缩邻香草醛席夫碱提供两个配位原子,中心Ni(Ⅱ)离子是一个六配位的畸变八面体结构。该聚合物中含有四个结晶水分子,水分子通过氢键作用,形成了一个六聚水簇。配合物分子通过氢键和π-π堆积作用形成三维超分子结构。 相似文献