The Interaction of Cobalt (Ⅲ) Mixed-Ligand Coordination Compound Containing Dipyrido[3,2-a:2′,3′-c] phenazine With Calf Thymus DNA -

The binding of Co (phen)2dppz3+ to calf thymus DNA,as investigated using absorption spectroscopy. viscosity and electrophoresis measurements,here dppz is dipyrido[3, 2-a: 2'3'-c]phenazine. The compound shows absorption hypochromicity and the specific viscosity increased upon binding to calf thymus DNA The complex is also shown to be more efficient photosensitisers for single strand breaks in plasmid DNA

Recent advances in cobalt-, nickel-, and iron-based chalcogen compounds as counter electrodes in dye-sensitized solar cells

The electroactive materials used in the counter electrode(CE)are of great concern as they influence the photovoltaic performances of dye-sensitized solar cells.The main functions of CE materials are collecting electrons from the external circuit and transferring them to the electrolyte and realizing the catalytic reduction of the redox species(I3^– or Co^3+)present in the electrolyte.The research hotspot of CE materials is seeking functional materials that display high efficiency,low cost,and good electrochemical stability and can substitute the benchmark platinum electrode.Chalcogen compounds of cobalt,nickel,and iron have been widely applied as CE materials and exhibit excellent electrocatalytic performances owing to their unique electrical properties,similar energies of adsorption of I atoms as platinum,excellent catalytic activities,and good chemical stabilities.In this review,we trace the developments and performances of chalcogen compounds of iron,cobalt,and nickel as CE materials and present the latest research directions for improving the electrocatalytic performances.We then highlight the optimization strategies for further improving their performances,such as fabrication of architectures,regulation of the components,synthesis of composites containing carbon materials,and elemental doping.

Synthesis,Crystal Structure and Electrochemical Properties of a Cobalt Compound Based on N-(4-pyridylmethyl)imidazole Ligand

One compound with N-（4-pyridylmethyl）imidazole liand, [Co（pyim）2（N3）2]n 1 （pyim = N-（4-pyridylmethyl）imidazolv）, was synthesized and structurally characterized. Compound 1 crystallizes in triclinic, space group P21/c with a = 8.090（3）, b = 16.109（3）, c = 8.590（3）, β = 117.800（12）°, V= 990.3（5） A3, Z= 2, Mr = 46137, Dc = 1.547 g/cm3, F（000） = 474, μ= 0.901 mml, the final R = 0.0381 and wR = 0.0950 for 1581 observed reflections with I〉 2o（I）. In this compound, the unique Co（II） resides at a crystallographic inversion center and exhibits an octahedral coordination geometry. The adjacent Co（II） ions are connected by the pyim ligands to form a 2D layer structure. The layers are stacked in an ABAB mode and reinforced by the weak interlayer C-H.-.N hydrogen bonds and π-π stacking to give a 3D architecture. The thermal properly and electrochemical property of compound 1 have also been studied.

Synthesis, structural and spectroscopic characterization of the bis(nitrito-<i>N</i>) octaethylporphyrin cobalt(III) complex

The bis(nitrito-N) cobalt(III) octaethylporphyrin derivative with the formula [K(18-C-6)(NO2)0.5(H2O)0.5]2 [CoIII(OEP)(NO2)2] (1) (OEP = octaethylporphyrin and 18-C-6 is the crown ether18-crown-6) has been synthesized and characterized by UV-vis, IR and proton NMR spectroscopy which indicate, inter alia, that the cobalt ion presents the oxidation state III. The synthesis utilizes 18-crown-6 to solubilize potassium nitrite in the synthetic procedure. This compound crystallizes in the triclinic system, with the centric space group P-1 and the following unit cell parameters: 11.6724(2) ?, b = 12.5715(2) ?, c = 13.4722(3) ?, α = 101.1290(6)°, β = 106.6498(6)°, γ= 109.1507(6)°, Z = 1 and V = 1696.74(5) ?3. The crystal structure has been solved and refined to R = 0.0499 and R(w) = 0.1319. The X-rays molecular structure of 1 shows that there is a relatively close interaction of both two NO2- axial ligands of the ion complex [CoIII(OEP)(NO2)2]- with the potassium atoms of the two counterions [K(18-C-6) (NO2)0.5(H2O)0.5]0.5+. The title compound exhibits one-dimension polymer-like structure where “monomers” are linked together through strong O(H2O)—H…O(nitrito-O) hydrogen bonds.

Synthesis and Crystal Structure of N-(2-Pyridylmethyl)-L-Alanine) Isothiocyanate Cobalt(III)

The title compound, [N-(2-pyridylmethyl)-(L)-alanine]Co(III) thiocyanate (1) was obtained from the reaction of Co(OOCH3)2·H2O with the tridentate reduced Schiff base ligand, N-(2-pyridylmethyl)-(L)-alanine (L) and NH4SCN and characterized by elemental analysis, IR, UV-visible, TGA and single- crystal X-ray diffraction. Structural and spectroscopic analyses reveal [Co(L)2)]SCN to be monomeric with Cobalt(III) adopting a pseudo-octahedral geometry, coordinating to two reduce Schiff base ligands. In the crystal lattice, the thiocyanate anion forms an intermolecular SCN···HNamine hydrogen bond, while adjacent monomers are linked by intermolecular Ocarboxyl···HNamine···H-bonds to form a supramolecular network. This work is therefore undertaken in an attempt to construct coordination framework structures of varying properties using the mixed-ligand strategy involving reduced Schiff bases and the thiocyanate ion.

Catalytic performance of cobalt oxide-supported gold-palladium nanocatalysts for the removal of toluene and o-xylene

Using the molten salt and polyvinyl alcohol-protected reduction method,we fabricated Co3O4 octahedron-supported Au-Pd（x（AuPdy）/Co3O4;x =（0.18,0.47,and 0.96） wt%;y（Pd/Au molar ratio） =1.85-1.97） nanocatalysts.The molten salt-derived Co3O4 sample possessed well-defined octahedral morphology,with an edge length of 300 nm.The Au-Pd nanoparticles,with sizes of 2.7-3.2 nm,were uniformly dispersed on the surface of Co3O4.The 0.96（AuPd1.92）/Co3O4 sample showed the highest catalytic activity for toluene and o-xylene oxidation,and the temperature required for achieving 90%conversion of toluene and o-xylene was 180 and 187 ℃,respectively,at a space velocity of 40000 mL/（g·h）.The high catalytic performance of Co3O4 octahedron-supported Au-Pd nanocatalysts was associated with the interaction between Au-Pd nanoparticles and Co3O4 and high concentration of adsorbed oxygen species.

基于四唑乙酸的二维Ce(III)配合物的合成、结构和光学性能研究

以四唑乙酸(Htza)与Ce(NO3)3·6H2O在少量三乙胺存在的CH3OH溶剂中,室温挥发的方法培养出无色配合物[Ce(tza)(3CH3OH)(H2O)]n.晶体结构分析表明,配合物属于单斜晶系P2(1)/n空间群.Ce(III)中心采取十配位的畸变双加冠四方反棱柱构型.四唑乙酸配体存在双齿桥联和双齿螯合桥联两种配位模式,通过羧酸上氧原子与铈配位形成一维的配位聚合物.链与链通过氮原子和配位水分子间氢键作用形成最终的二维网状结构.对配合物的红外和紫外可见光谱性质也进行了研究.

Cobalt-catalyzed redox-neutral synthesis of isoquinolines: C–H activation assisted by an oxidizing N–S bond

A redox‐neutral avenue to access isoquinolines has been realized by a Co（III）‐catalyzed C–H activa‐tion process. Starting from readily available N‐sulfinyl imine substrates and alkynes, the reaction occurred via N–S cleavage with broad substrate scope and functional group compatibility in the presence of cost‐effective cobalt catalysts.

Synthesis and Crystal Structure of Trans-diaquabis(hexamethylenetetramine-N)bis(isothiocyanato)cobalt(Ⅱ) trans-tetraaquabis(isothiocyanato)cobalt(Ⅱ) dihydrate

The synthesis and crystal structure of [Co(NCS)2(hmt)2(H2- O)2]穂Co(NCS)2(H2O)4]?H2O (hmt = hexamethylenetetramine) are reported. The crystal belongs to triclinic, space group P with unit cell parameters: a = 7.917(1), b = 9.023(1), c = 12.877(1) ? ?= 94.21(1), = 96.68(1), ?= 115.42(1)? C16H40Co2N12O8S4, Mr = 774.7, V = 817.33 3, Z = 1, Dc = 1.574 g/cm3, F(000) = 402 and (MoK? = 1.328mm-1. The final values of R and wR are 0.0251 and 0.0598, respectively, for 2545 observed reflections with I > 2(I). Each Co atom is in an octahedral coordination environment, and the independent uncharged components [Co(NCS)2(hmt)2(H2O)2], [Co(NCS)2(H2O)4] and H2O are linked together by three kinds of hydrogen bonds (O(2)H贩種(3) and O(3)H贩種(2), O(1)H贩稯(4) and O(3)H贩稯(4), O(2)H贩稴(2) and O(4)H贩稴(1)) to form a three-dimensional supramolecular architecture.

Crystal Structure and Magnetic Properties of a Two-dimensional Compound{(Me2NH2)4[Co(SIP)2]·2(DMF)·3(H2O)}n

-

HPLC法测定复方盐酸普鲁卡因溶液III中盐酸普鲁卡因的含量

目的 建立以高效液相色谱法测定复方盐酸普鲁卡因溶液III中盐酸普鲁卡因含量的方法.方法 采用高效液相色谱法,用Ultimate LP-C18色谱柱（4.6 mm×0 mm,5 μm）,以0.1%庚烷磺酸钠的0.05 mol·L-1磷酸二氢钾溶液（用磷酸调pH至3.0）-甲醇（68∶ 32）为流动相,流速为1.0 mL·min-1,检测波长为290 nm.结果 盐酸普鲁卡因线性范围为10.66～106.6 μg·mL-1（r=0.999 7）,平均加样回收率为99.2%（RSD=0.8%）.结论 该方法快速、方便,操作简单,其他成分无干扰,适用于测定复方盐酸普鲁卡因溶液III中盐酸普鲁卡因的含量.

Optical properties of cobalt xanthate films on different substrates

Cobalt isopropyl xanthate thin films （CXTFs） were deposited via chemical bath deposition onto different substrates：commercial glass （CG）, indium tin oxide （ITO）, and poly（methyl methacrylate） （PMM）. Isopropyl xanthate was synthesized according to a method described in the literature. The cobalt nitrate and isopropyl xanthate were mixed in a beaker, which allowed the thin films to be deposited via a simple ion-ion mechanism. The transmission, reflectivity, refractive index, dielectric constant, and optical conductivity were investigated for various thin films coated onto different substrates. An ultraviolet-visible spectrophotometer was used to measure the optical properties of the thin films. The lowest value of the transmission and the highest value of the refractive index were observed for the thin films deposited onto PMM. The structure of the cobalt xanthate was characterized by Fourier transform infrared （FTIR） spectroscopy, which was measured using a Perkin-Elmer Spectrum 400 spectrometer. The stretching vibration of the Co-S bonds was observed at 359 cm^-1 in the FTIR spectrum of the CXTFs.

A PRELIMINARY STUDY ON THE STABILITY OF TERNARY CoCl_2-FeCi_3 GRAPHITE INTERCALATION COMPOUNDS

The ternary CoCl2-FeCl3 graphite intercalation compounds (CoCl2-FeCl3 G/C) have been subjected to different treatments in various media. It is found that the CoCl2-FeCl3 GIC is stable 'when it is stored under conditions of opening to at-mosphere,whereas,acids,NaOH,boiling water,and heat treat-ments have different effects on the stability of the CoCl2-FeCl3 G/C.

Synthesis and Crystal Structure of a Cobalt(Ⅱ)Complex Based on 2,2-Bibenzimidazole and N,N-bis(phosphonomethyl)aminoacetic Acid

The title complex, [Co2（bibzim）（H2bibzim）4]·Co2（H2bibzim）2（Hbibzim）（HL）]2- 2H2O （1） （HEbibzim = 2,2＇-bibenzimidazole, H5L = N,N-bis（phosphonomethyl）aminoacetic acid （HO2CCH2N（CH2PO3H2）2））, was synthesized with hydrothermal reactions. The compound crystallizes in triclinic, space group P1 with a = 13.71020（10）, b = 14.9165（5）, c = 20.9924（5） A, a = 86.344（9）, β = 71.214（8）, γ = 73.757（7）°, C162HI24Co6N46O18P4, Mr = 3478.52, V = 3900.55（16） A3, Z = 2, Dc = 1.482 g/cm3,μ（MoKa） = 0.747 mm^-1, F（000） = 1784, the final R = 0.0777 and wR = 0.2091 for 13598 observed reflections （I 〉 2σ（I））. X-ray diffraction analysis reveals that there are three crystallographically independent Co（II） atoms in the complex. The complex consists of binuclear coordination cation, binuclear coordination anion, as well as lattice water molecules, which further aggregate into a 3D framework via hydrogen bonding as well as π-π interactions.

Synthesis and Crystal Structure of a Novel Compound:[Nd_3(OH)_7(O_2CC_6H_4SO_3)(H_2O)]_n·nH_2O with a Pillar-layered Structure

A novel Nd（Ⅲ） compound,[Nd3（OH）7（O2CC6H4SO3）（H2O）]n·nH2O 1,has been synthesized by the hydrothermal reaction of Nd2O3 and 3-sulfobenzoic acid monosodium salt. It was characterized by IR spectroscopy,elemental analysis,thermogravimetric analysis and single-crystal X-ray diffraction. It crystallizes in monoclinic,space group P21/c with a = 13.024（3）,b = 10.961（2）,c = 12.792（3） ,β = 91.271（3）°,V = 1825.6（7） 3,Z = 4,Mr = 787.97,Dc = 2.867 g/cm3,μ = 8.584 mm-1,F（000） = 1460,S = 1.035,R = 0.0442 and wR = 0.1166 （I 〉 2σ（I））. In this compound,the cross-linkage of Nd atoms by bridging hydroxy groups results in a Nd-O inorganic 〈200〉 layer,and such layers are linked by the 3-O3S-C6H4-CO2 dianions into a pillar-layered structure. The lattice water molecules are located in the cavity.

A Chiral Three Dimensional Potassium(I)/Strontium(II)/Chromium(III) Oxalato-Bridged Coordination Polymer: Synthesis, Characterization and Thermal Analysis

A new compound of general formula {[(H2O)2K(μ-H2O)Sr]@[Cr(C2O4)3]}n (1) has been synthesized in water and characterized by elemental and thermal analyses, EDX, IR and UV-Vis spectroscopies and by single crystal X-ray structure determination. Compound 1 crystallizes in the chiral space group Fdd2 of orthorhombic system with a = 14.110 (4) ?, b = 36.074 (11)?, c =11.034 (3)? and Z = 16. Compound 1 is a coordination polymer in which the three-dimensional lattice framework is realized by the interconnectivity between K+ cations, Sr2+ cations, aqua ligands and [Cr(C2O4)3]3– complex anions. The asymmetric unit of 1 consists of one cationic motif formally written [(H2O)2K(μ-H2O)Sr]3+ and one anionic entity, [Cr(C2O4)3]3–. The K+ and Sr2+ ions in the cationic motif are both eight-coordinate while the Cr3+ ions in the anionic complex are six-coordinate in a distorted octahedral geometry. Coulombic interactions between the ionic motifs and the three-dimensional H-bonding involving aqua ligands help to consolidate the bulk structure. Thermogra-vimetric analysis (TGA) shows that compound 1 is stable to heat up to ca. 80℃.

Synthesis, Characterization and Crystal Structure of Cobalt(II) Complex of a Schiff Base Derived from Isoniazid and Pyridine-4-Carboxaldehyde

A new hydrogen bonded Cobalt(II) Schiff base complex,?N’-(pyridine-4-carboxaldehyde) isonicotinoylhydrazone Cobalt(II), has been synthesized from isoniazid and pyridine-4-carboxaldehyde and characterized by IR spectroscopy, 1H-NMR, elemental analysis, TGA and single crystal X-ray structure determination. X-ray crystal structure analysis shows an octahedral complex with a metal centre coordinated to two ligand molecules through the pyridine nitrogen atoms and four water molecules and containing two nitrate groups as counter ions. The complex crystallizes in the monoclinic crystal system and P2(1)/n space group. The unit cell dimensions are: a = 7.2108(4) &Aring;, b = 16.6020(9) &Aring;, c = 13.0389(6) &Aring;,α = 90°, β = 103.972(4)°, γ = 90°. The molecule is symmetrical about the cobalt centre as observed from the 1H-NMR and 13C-NMR and confirmed by the single crystal X-ray structure of the complex. Thermogravimetric analysis shows two steps decomposition of the complex to leave a metal oxide residue. The title compound is expected to be biologically active as one of the precursors (isoniazid) is a therapeutic agent with well-established clinical applications.

Co-MOFs衍生的钴基化合物催化氧化典型VOCs研究进展

基于催化氧化技术在挥发性有机化合物(VOCs)末端治理方面有极高的效率,以及近年来金属有机骨架(MOFs)衍生的钴基化合物在催化氧化VOCs中的优异表现,文章总结了4种典型的钴基MOFs(ZIF-67,ZSA-1,Co-MOF-71和Co-MOF-74)及其衍生的钴基催化剂的组成与制备方法,并综述了其衍生物催化氧化几种典型VOCs(甲苯、邻二甲苯、甲醛和丙酮)的研究进展。最后归纳了反应过程中空速和湿度等因素对钴基化合物催化氧化VOCs的影响,探讨了MOFs衍生的钴基催化剂的反应机理,并对MOFs衍生的钴基催化剂在VOCs氧化中的研究进行了展望。

NiCo-LDH材料的形貌分析与电化学性能研究

采用一步水热法在泡沫镍上合成镍钴层状双金属氢氧化物(NiCo-LDH)电极材料,用扫描电镜分析电极材料的微观形貌,X射线衍射仪分析电极材料的物相,并在不同扫描速率以及不同电流密度下NiCo-LDH纳米材料进行了电化学性能测试。结果表明:随着尿素含量的增加,NiCo-LDH的形貌由六角片状、草丛状,最后形成片层上带有针状形貌。扫描速率为10 mV·s^(-1)时,在CV曲线中可以清晰地看到氧化还原峰。电极在0.30~0.35V之间的充放电曲线出现对称的充放电平台,说明其充放电容量和充放电时间均较优,该复合材料的电容性能良好。

湿法炼锌钴镍渣综合回收的试验研究

针对传统硫酸浸出湿法炼锌钴镍渣回收率低的情况,采用“酸洗-焙烧-选择性浸出”工艺进行处理。通过试验得到工艺的最佳条件:酸洗,L/S=3~4∶1、温度60~65℃、pH为1.5~2.0、反应时间0.5 h;焙烧,焙烧时间0.5 h;浸出,温度60~65℃、pH为4.5~5.0、L/S=3~4∶1、反应时间4 h。用该工艺对某钴镍3#渣进行处理,结果表明94%的锌可溶出,94%的钴、镍被富集在渣中,富集比为7。