A novel pyrazine-2,3-dicarboxylic acid bridged Co(II) phen complex 2 ∞ [Co- ...A novel pyrazine-2,3-dicarboxylic acid bridged Co(II) phen complex 2 ∞ [Co- (phen)(μ-L)3/3]?H2O (H2L = pyrazine-2,3-dicarboxylic acid) has been hydrothermally synthesized, and X-ray single-crystal diffraction analysis shows that it crystallizes in the monoclinic system, space group P21/n with a = 11.480(2), b = 11.885(2), c = 12.939(3) ?, β = 110.55(3)°, V = 1653.1(6) ?3, Mr = 423.25, Dc = 0.425 g/cm3, Z = 4, R = 0.0361 and wR = 0.1011. The title complex consists of 2D 2 ∞ [Co(phen)(μ-L)3/3] layers and crystal water molecules. Each Co atom is octahedrally coordinated by three N atoms and three O atoms to form 2D 2 ∞ [Co(phen)(μ-L)3/3] polymeric layers. Furthermore, such 2D layers are stacked into 3D supramolecular frameworks via Van der Waals’ intermolecular forces, strong and weak hydrogen-bond interactions. The coordination phen and crystal water molecules are resided into cavities of the frameworks.展开更多
The title nickel complex I and cobalt complex II were obtained separately from the direct reaction of D-（＋）-leucinol with Ni（II） chloride and L-（-）-leucinol with Co（II） acetate tetra- hydrate in anhydrous met...The title nickel complex I and cobalt complex II were obtained separately from the direct reaction of D-（＋）-leucinol with Ni（II） chloride and L-（-）-leucinol with Co（II） acetate tetra- hydrate in anhydrous methanol. The crystal structures of I and II were determined by single-crystal X-ray diffraction and further characterized by elemental analysis and IR. For I： [Ni（C18H45N3O3）]Cl2, orthorhombic, P212121, a = 11.2807（9）, b = 14.7115（11）, c = 16.3580（13） A, V = 2714.7（4） A3, Z = 4, Pcalcd = 1.177 Mg/m3, the final R = 0.0407, and 16539 reflections observed with I 〉 2σ（/）; For II： [Co（C45HI08N6015）], trigonal, R3：H, a = 23.981（3）, b =23.981（3）, c = 10.8925（15） A, γ = 120°, V = 5425.1（14） A3, Z = 3, Pcalcd = 1.002 Mg/m3, the final R = 0.0625 for 16556 observed reflections with I 〉 2σ（I）. The complexes were then used to catalyze the Henry reaction and obtained good catalytic results. The catalytic activity of the complexes was determined by IH NMR. And research is going towards the application to other organic reactions such as cyanosilylation reaction.展开更多
The taxonomic status of Papilio maackii and P.syfanius has long been disputed.We conducted a molecular phylogenetic study to evaluate the taxonomic status of P.maackii and P.syfanius.A total of twenty-four P.maackii i...The taxonomic status of Papilio maackii and P.syfanius has long been disputed.We conducted a molecular phylogenetic study to evaluate the taxonomic status of P.maackii and P.syfanius.A total of twenty-four P.maackii individuals from six localities and sixteen P.syfanius individuals from two localities were analyzed.We sequenced the partial region of the CO-I gene（about 579 bp） and partial CO-II gene sequence（about 655bp） of the two species.The Kimura-2-Parameter distances among P.maackii and P.syfanius ranged from 0 to 0.6%.Fifteen haplotypes were obtained based on the combined data set.The results strongly supported that all P.maackii individuals and all P.syfanius individuals formed a large clade,and could not be divided into separated clades.This research indicated that the two species have only very recently undergone speciation.展开更多
A novel surface ion implinted adsorbent [Co（II）-IIP] using polyethyleneimine （PEI） as function monomer and ordered mesoporous silica SBA-15 as support matrix was prepared for Co（II） analysis with high selectivit...A novel surface ion implinted adsorbent [Co（II）-IIP] using polyethyleneimine （PEI） as function monomer and ordered mesoporous silica SBA-15 as support matrix was prepared for Co（II） analysis with high selectivity. The prepared polymer was characterized by Fourier transmission infrared spectrometry, scanning electron microscopy, X-ray diffraction and nitrogen adsorption-desorption isotherm. Bath experiments of Co（II） adsorption onto Co（II）-IIP were performed under the optimum conditions. The experimental data were analyzed by pseudo-first-order and pseudo-second-order kinetic models. It was found that the pseudo-second-order model best correlated the kinetic data. The intraparticle diffusion and liquid film diffusion were applied to discuss the adsorption mechanism. The results showed that Co（II） adsorption onto IIP was controlled by the intraparticle diffusion mechanism, along with a considerable film diffusion contribution. Langmuir, Freundlich and Dubinin-Radushkevich adsorption models were applied to determine the isotherm parameters. Langmuir model fitted the experiment data well and the maximum calculated capacity of Co（II） reached 39.26 mg/g under room temperature. The thermodynamic data were indicative of the spontaneousness of the endothermic sorption process of Co（II） onto Co（II）-IIP. Co（II）-IIP showed high affinity and selectivity for template ion compared with non imprinted polymer （NIP）.展开更多
A new 1D coordination polymer [Co（bpp）3Cl2（H2O）2]n 1 （bpp = 1,3-bis（4-pyridyl）-propane） was synthesized and characterized by elemental analysis,IR spectrum and single-crystal X-ray diffraction. The crystal bel...A new 1D coordination polymer [Co（bpp）3Cl2（H2O）2]n 1 （bpp = 1,3-bis（4-pyridyl）-propane） was synthesized and characterized by elemental analysis,IR spectrum and single-crystal X-ray diffraction. The crystal belongs to the orthorhombic system,space group Ibca with a = 16.569（9）,b = 17.240（10）,c = 27.087（16） ,V = 7738（8） 3,Z = 8,Dc = 1.306 g/cm3,Mr = 760.65,λ（MoKa） = 0.71073 ,μ = 0.623 mm1,F（000） = 3192,the final R = 0.0678 and wR = 0.2011. The Co（II） atom is coordinated in a slightly distorted octahedral CoN4Cl2 geometry by two Cl atoms in the axial positions,four N atoms from the two bridging bpp ligands and two pendant bpp ligands. The CoN4Cl2 octahedra are connected by the bridging bpp ligands to form a 1D neutral coordination polymer chain. The chains are linked by face-to-face π-π interactions between adjacent pendant bpp ligands to give rise to a 3D supramolecular architecture. The photoluminescent investigation indicates that the emission of 1 is attributed to ligand-centered emission. The variable-temperature magnetic susceptibility measurement shows weak antiferromagnetic behavior in the coπmplex.展开更多
The Co（II） complex I and ammonium salt II were synthesized from the direct reaction of 1,2-ethylenediamine and cobaltous acetate tetrahydrate and manganese acetate tetrahydrate in anhydrous ethanol. Treatment of N,N...The Co（II） complex I and ammonium salt II were synthesized from the direct reaction of 1,2-ethylenediamine and cobaltous acetate tetrahydrate and manganese acetate tetrahydrate in anhydrous ethanol. Treatment of N,N＇-bis（salicylidene）ethylenediamine with Cu（OAc）2·H2O results in the formation of Cu（II） complex III. C14H37CoNaO8 （I）： triclinic, space group P1, a = 8.6296（12）, b = 12.0291（17）, c = 12.1108（17） A, α = 75.335（2）, β = 69.991（2）, γ = 72.248（2）°, V= 1109.4（3） A3, Z = 2, ρcaloa = 1.342 g/cm3, the final R= 0.0342 for 4817 observed reflections with I 〉 2σ（I） and Rw = 0.1263 for all data. C6H16N204 （II）： space group P1, a = 5.5513（10）, b = 5.5589（11）, c = 7.4437（14） A, α = 94.332（4）, β = 104.497（4）, γ = 103.487（4）°,V= 214.06（7） A3, Z = 1, ρcalcd = 1.398 g/cm3, the final R = 0.0431 for 829 observed reflections with I〉 2σ（I） and Rw = 0.1263 for all data. C14H37CuN40 （III）, space group P21/n, a = 9.050（9）, b = 18.434（17）, c = 11.659（11） A, β = 107.134（19）°, V= 1859（3） A3, Z = 4, ρcalcd =1.443 g/cm3, the final R = 0.0616 for 3308 observed reflections （O 〉 2σ（I）） and Rw = 0.1229 for all data. Their structures were all determined by X-ray diffraction, elemental analysis and IR.展开更多
Adsorption of Cu(II) and Co(II) from aqueous solutions on synthetic nano Fe3O4 has been studied. The effect of experimental parameters such as initial concentration of the metal ions, adsorbent dosage, contact time an...Adsorption of Cu(II) and Co(II) from aqueous solutions on synthetic nano Fe3O4 has been studied. The effect of experimental parameters such as initial concentration of the metal ions, adsorbent dosage, contact time and pH has been investigated. Optimum removal efficiency of Cu(II) ion was found to be 97.8% with the dose rate of 1.07 g/L in 60 minutes at pH = 5.5 and for Co(II) ion, it was found to be 99.2% with the dose rate of2.57 g/L in 10 minutes at pH = 5.4. The removal of Co(II) ions require only 10 minutes with the efficient removal of 99.2%, whereas Cu(II) ions require 60 minutes with the maximum removal of 97.8%. In order to understand the effective removal of Cu(II) and Co(II) ions on Fe3O4, room temperature magnetic measurement was carried out using Vibrational Spectrum Magnetometer (VSM), before and after adsorption with a maximum applied magnetic field of 20,000 G.展开更多
Cobalt and copper recovery from aqueous Co （II） and Cu（II） is one critical step for cobalt and copper wastewaters treatment. Previous tests have primarily examined Cu（II） and Co（II） removal in microbial electr...Cobalt and copper recovery from aqueous Co （II） and Cu（II） is one critical step for cobalt and copper wastewaters treatment. Previous tests have primarily examined Cu（II） and Co（II） removal in microbial electro- lysis cells （MECs） with abiotic cathodes and driven by microbial fuel cell （MFCs）. However, Cu（II） and Co（II） removal rates were still slow. Here we report MECs with biocathodes and driven by MFCs where enhanced removal rates of 6.0＋0.2mg·L^-1·h^-1 for Cu（II） at an initial concentration of 50 mg·L^-1 and 5.3~0.4mg·L^-1·h^-1 for Co（II） at an initial 40 mg· L^-1 were achieved, 1.7 times and 3.3 times as high as those in MECs with abiotic cathodes and driven by MFCs. Species of Cu（II） was reduced to pure copper on the cathodes of MFCs whereas Co（II） was removed associated with microorganisms on the cathodes of the connected MECs. Higher Cu（II） concentrations and smaller working volumes in the cathode chambers of MFCs further improved removal rates of Cu（II） （115.7 mg·L^-1·h^-1） and Co（II） （6.4 mg·L^-1·h^-1） with concomi- tantly achieving hydrogen generation （0.054-0.00 mol·mol^-1 COD）. Phylogenetic analysis on the bio- cathodes indicates Proteobacteria dominantly accounted for 67.9% of the total reads, followed by Firmicutes （14.0%）, Bacteroidetes （6.1%）, Tenericutes （2.5%）, Lentisphaerae （1.4%）, and Synergistetes （1.0%）. This study provides a beneficial attempt to achieve simultaneous enhanced Cu（II） and Co（II） removal, and efficient Cu（II） and Co（II） wastewaters treatment without any external energy consumption.展开更多
Two three-dimensional supramolecular water architectures,[Zn(phen)3]2 ·[Zn(C10H16O4)·(H2O)3]·(C10H16O4)2·20H2O(1) and [Co(phen)3]2 ·[Co(H2O)6]·(C10H16O4)3·30H2O(2)[phen=1,10-Phenanth...Two three-dimensional supramolecular water architectures,[Zn(phen)3]2 ·[Zn(C10H16O4)·(H2O)3]·(C10H16O4)2·20H2O(1) and [Co(phen)3]2 ·[Co(H2O)6]·(C10H16O4)3·30H2O(2)[phen=1,10-Phenanthroline,C10H16O4=sebacic dianion],have been synthesized and characterized by IR,elemental analysis,thermogravimetric analysis,and single-crystal X-ray diffractions.The two structures both contain extensive hydrogen bonding between water molecules as well as between water molecules and sebacic anions.The water molecules and sebacic acid O atoms assembled 2D supramolecular corrugated sheets with different morphology in the two complexes.展开更多
Two new one-dimensional chain-like coordination polymers,[Cu（H2O）（dpa）- MoO4]·H2O 1 and [Co（H2O）（dpa）MoO4] 2,have been synthesized under hydrothermal reactions. Their structures were determined by single-...Two new one-dimensional chain-like coordination polymers,[Cu（H2O）（dpa）- MoO4]·H2O 1 and [Co（H2O）（dpa）MoO4] 2,have been synthesized under hydrothermal reactions. Their structures were determined by single-crystal X-ray diffraction analysis. Crystal data for 1： [Cu（H2O）（dpa）MoO4]·H2O,Mr = 430.71,monoclinic,space group P21/c,a = 9.5469（10）,b = 16.6874（17）,c = 9.0799（10）A,β = 104.9100（10）°,V = 1397.8（3）A^3,Z = 4,Dc = 2.047 g/cm^3,F（000） = 852,μ = 2.449 mm-1,the final R = 0.0293 and wR = 0.0638 for 2472 independent reflections （Rint = 0.0338） and 2034 observed reflections with I 〉 2σ（I）. Crystal data for 2： [Co- （H2O）（dpa）MoO4],Mr = 408.09,monoclinic,space group P21/c,a = 10.204（2）,b = 18.933（4）,c = 6.8875（16）A,β = 102.195（3）o,Z = 4,V = 1300.5（5）A^3,Z = 4,Dc = 2.084 g/cm3,F（000） = 804,μ = 2.262 mm-1,the final R = 0.0357 and wR = 0.0693 for 3022 independent reflections （Rint = 0.0436） and 2286 observed reflections （I 〉 2σ（I））. Polymer 1 is based on a one-dimensional zigzag chain built up from {Cu（H2O）（dpa）}2＋ units bridged through the bidentate {MoO4}2- ligands. The chains extending along the c-axis are arranged alternately with two opposite orientations along the b-axis. The adjacent chains are stably packed together through π-π interactions and exhibit an interesting three-dimensional supramolecular architecture via hydrogen bonding interactions. Polymer 2 based on a one-dimensional zonal chain is built up from {Co（H2O）（dpa）}2＋ units linked by the tridentate {MoO4}2- ligands. The ribbons extend along the c-axis. In the bc layers,there are significant interactions of N-H…O-Mo hydrogen bonds and π-π overlaps of dpa ligands between adjacent ribbons.展开更多
The reaction of bis-[2-amino-4-pheny1-5-thiazolyl] disulfide with 5-nitro-salicylaldehyde in absolute ethanol resulted in the formation of a new Schiff base ligand H<sub>2</sub>L (1). Characterization of t...The reaction of bis-[2-amino-4-pheny1-5-thiazolyl] disulfide with 5-nitro-salicylaldehyde in absolute ethanol resulted in the formation of a new Schiff base ligand H<sub>2</sub>L (1). Characterization of the ligand was performed by FT-IR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, UV-Vis, elemental analysis and single crystal X-ray diffraction. The ligand, (1), possesses a disulfide –S–S– bridge of 2.1121 (3) ? length, and the molecule adopts a cis-conformation around this bond. In the crystal structure of (1), an intramolecular O–H···N hydrogen bond with D… A distance of 2.69 (3) ? was present. The reaction of (1) with Co(NO<sub>3</sub>)<sub>2</sub>·6H<sub>2</sub>O and CuCl<sub>2</sub>·2H<sub>2</sub>O in methanol afforded the corresponding metal complexes. The obtained solids were further investigated by elemental analysis and UV-Vis titration that confirmed the formation of [CoL] and [ClCuHL] complexes. However, recrystallizaion of the Co(II) complex in dimethylsulfoxide caused the complete hydrolysis of the imine bond and afforded a Co(II) complex in which two 5-nitro-salicylaldehyde and two DMSO molecules were coordinated to the central metal in an octahedral fashion. This structure (2) was also confirmed by single crystal X-ray analysis.展开更多
A novel chemiluminescence (CL) sensor for H2O2 combined with flow injection analysis is described in this paper. H2O2 is sensed by the CL reaction with luminol and Co2+ bleeding from the ion exchange column with immob...A novel chemiluminescence (CL) sensor for H2O2 combined with flow injection analysis is described in this paper. H2O2 is sensed by the CL reaction with luminol and Co2+ bleeding from the ion exchange column with immobilized reagents by hydrolysis. The calibration graph is linear and falls between the range of 4x10(-8) to 1x10(-5) mol/L. A complete analysis could be performed in 1 min. The system was reused for over 50 hours.展开更多
The cobalt（II） complex with （quinolin-8-yloxy）acetate, [CoCl（C11H8NO3）]n （1）, has been prepared via the solvothermal method and characterized by IR, elemental analysis, UV- Vis diffuse-reflection spectra and s...The cobalt（II） complex with （quinolin-8-yloxy）acetate, [CoCl（C11H8NO3）]n （1）, has been prepared via the solvothermal method and characterized by IR, elemental analysis, UV- Vis diffuse-reflection spectra and single-crystal X-ray diffraction analysis. Complex 1 is a novel carboxylate-bridged one-dimensional helical cobalt（II） polymer, and the Co（II） centre exhibits an approximately square pyramidal CoClNO3 coordination geometry. It crystallizes in monoclinic, space group P21/n, with a = 9.1594（10）, b = 6.8864（7）, c = 17.290（2） , β = 102.629（3）o, C11H8ClCoNO3, Mr = 296.56, V = 1064.2（2） 3, Z = 4, Dc = 1.851 g/cm3, F（000） = 596, μ = 1.856 mm-1, the final R = 0.0308 and wR = 0.0807. Interestingly, the chain complexes are assembled to form two-dimensional networks through intermolecular face-to-face π-π stacking interactions with the centroid-to-centroid distance of 3.559（1） and the dihedral angle of 8.4（1）° between the aromatic rings.展开更多
A study on the removal of Co（Ⅱ） from aqueous solutions by water treatment residuals（WTR） was conducted in batch conditions. The sorption process of Co（Ⅱ） followed pseudosecondorder kinetics, with 30 hr require...A study on the removal of Co（Ⅱ） from aqueous solutions by water treatment residuals（WTR） was conducted in batch conditions. The sorption process of Co（Ⅱ） followed pseudosecondorder kinetics, with 30 hr required to reach equilibrium. Using the Langmuir adsorption isotherm model, a relatively high maximum sorption capacity of 17.31 mg/g Co（Ⅱ） was determined. The adsorption of Co（Ⅱ） was dependent on pH values and was affected by the ionic strength. Results show that Co（Ⅱ） adsorption was a spontaneous endothermic process and was favorable at high temperature. Most of the adsorbed Co（Ⅱ） stayed on the WTR permanently, whereas only small amounts of adsorbed Co（Ⅱ） were desorbed. The shifting of peaks in FT-IR spectra indicated that Co（Ⅱ） interacted with the WTR surface through strong covalent bond formation with Fe（Al）–O functional groups. It was concluded that WTR can be a suitable material from which to develop an efficient adsorbent for the removal of Co（Ⅱ） from wastewater.展开更多
基金This work was supported by the Science and Technology Bureau of Jinhua City (No 2003-01-179)
文摘A novel pyrazine-2,3-dicarboxylic acid bridged Co(II) phen complex 2 ∞ [Co- (phen)(μ-L)3/3]?H2O (H2L = pyrazine-2,3-dicarboxylic acid) has been hydrothermally synthesized, and X-ray single-crystal diffraction analysis shows that it crystallizes in the monoclinic system, space group P21/n with a = 11.480(2), b = 11.885(2), c = 12.939(3) ?, β = 110.55(3)°, V = 1653.1(6) ?3, Mr = 423.25, Dc = 0.425 g/cm3, Z = 4, R = 0.0361 and wR = 0.1011. The title complex consists of 2D 2 ∞ [Co(phen)(μ-L)3/3] layers and crystal water molecules. Each Co atom is octahedrally coordinated by three N atoms and three O atoms to form 2D 2 ∞ [Co(phen)(μ-L)3/3] polymeric layers. Furthermore, such 2D layers are stacked into 3D supramolecular frameworks via Van der Waals’ intermolecular forces, strong and weak hydrogen-bond interactions. The coordination phen and crystal water molecules are resided into cavities of the frameworks.
文摘The title nickel complex I and cobalt complex II were obtained separately from the direct reaction of D-（＋）-leucinol with Ni（II） chloride and L-（-）-leucinol with Co（II） acetate tetra- hydrate in anhydrous methanol. The crystal structures of I and II were determined by single-crystal X-ray diffraction and further characterized by elemental analysis and IR. For I： [Ni（C18H45N3O3）]Cl2, orthorhombic, P212121, a = 11.2807（9）, b = 14.7115（11）, c = 16.3580（13） A, V = 2714.7（4） A3, Z = 4, Pcalcd = 1.177 Mg/m3, the final R = 0.0407, and 16539 reflections observed with I 〉 2σ（/）; For II： [Co（C45HI08N6015）], trigonal, R3：H, a = 23.981（3）, b =23.981（3）, c = 10.8925（15） A, γ = 120°, V = 5425.1（14） A3, Z = 3, Pcalcd = 1.002 Mg/m3, the final R = 0.0625 for 16556 observed reflections with I 〉 2σ（I）. The complexes were then used to catalyze the Henry reaction and obtained good catalytic results. The catalytic activity of the complexes was determined by IH NMR. And research is going towards the application to other organic reactions such as cyanosilylation reaction.
基金National Natural Science Foundation of China (30870359)Anhui Scholar Special Fund in Science and Technology (KJ2009B015)
文摘The taxonomic status of Papilio maackii and P.syfanius has long been disputed.We conducted a molecular phylogenetic study to evaluate the taxonomic status of P.maackii and P.syfanius.A total of twenty-four P.maackii individuals from six localities and sixteen P.syfanius individuals from two localities were analyzed.We sequenced the partial region of the CO-I gene（about 579 bp） and partial CO-II gene sequence（about 655bp） of the two species.The Kimura-2-Parameter distances among P.maackii and P.syfanius ranged from 0 to 0.6%.Fifteen haplotypes were obtained based on the combined data set.The results strongly supported that all P.maackii individuals and all P.syfanius individuals formed a large clade,and could not be divided into separated clades.This research indicated that the two species have only very recently undergone speciation.
基金Project supported by the National Natural Science Foundation of China （No. 21077046）, Ph. D. Programs Foundation of Ministry of Education of China （No. 20093227110015）, Ph.D. Innovation Programs Foundation of Jiangsu University （No. CX09B 12XZ）.
文摘A novel surface ion implinted adsorbent [Co（II）-IIP] using polyethyleneimine （PEI） as function monomer and ordered mesoporous silica SBA-15 as support matrix was prepared for Co（II） analysis with high selectivity. The prepared polymer was characterized by Fourier transmission infrared spectrometry, scanning electron microscopy, X-ray diffraction and nitrogen adsorption-desorption isotherm. Bath experiments of Co（II） adsorption onto Co（II）-IIP were performed under the optimum conditions. The experimental data were analyzed by pseudo-first-order and pseudo-second-order kinetic models. It was found that the pseudo-second-order model best correlated the kinetic data. The intraparticle diffusion and liquid film diffusion were applied to discuss the adsorption mechanism. The results showed that Co（II） adsorption onto IIP was controlled by the intraparticle diffusion mechanism, along with a considerable film diffusion contribution. Langmuir, Freundlich and Dubinin-Radushkevich adsorption models were applied to determine the isotherm parameters. Langmuir model fitted the experiment data well and the maximum calculated capacity of Co（II） reached 39.26 mg/g under room temperature. The thermodynamic data were indicative of the spontaneousness of the endothermic sorption process of Co（II） onto Co（II）-IIP. Co（II）-IIP showed high affinity and selectivity for template ion compared with non imprinted polymer （NIP）.
基金supported by the National High Technology Research and Development Program of China (863 Program) (No. SQ2008AA03Z2470974)the National Natural Science Foundation of China (Nos. 50572030 and 50372022)the Young Talent Program of Fujian Province (No. 2007F3060)
文摘A new 1D coordination polymer [Co（bpp）3Cl2（H2O）2]n 1 （bpp = 1,3-bis（4-pyridyl）-propane） was synthesized and characterized by elemental analysis,IR spectrum and single-crystal X-ray diffraction. The crystal belongs to the orthorhombic system,space group Ibca with a = 16.569（9）,b = 17.240（10）,c = 27.087（16） ,V = 7738（8） 3,Z = 8,Dc = 1.306 g/cm3,Mr = 760.65,λ（MoKa） = 0.71073 ,μ = 0.623 mm1,F（000） = 3192,the final R = 0.0678 and wR = 0.2011. The Co（II） atom is coordinated in a slightly distorted octahedral CoN4Cl2 geometry by two Cl atoms in the axial positions,four N atoms from the two bridging bpp ligands and two pendant bpp ligands. The CoN4Cl2 octahedra are connected by the bridging bpp ligands to form a 1D neutral coordination polymer chain. The chains are linked by face-to-face π-π interactions between adjacent pendant bpp ligands to give rise to a 3D supramolecular architecture. The photoluminescent investigation indicates that the emission of 1 is attributed to ligand-centered emission. The variable-temperature magnetic susceptibility measurement shows weak antiferromagnetic behavior in the coπmplex.
文摘The Co（II） complex I and ammonium salt II were synthesized from the direct reaction of 1,2-ethylenediamine and cobaltous acetate tetrahydrate and manganese acetate tetrahydrate in anhydrous ethanol. Treatment of N,N＇-bis（salicylidene）ethylenediamine with Cu（OAc）2·H2O results in the formation of Cu（II） complex III. C14H37CoNaO8 （I）： triclinic, space group P1, a = 8.6296（12）, b = 12.0291（17）, c = 12.1108（17） A, α = 75.335（2）, β = 69.991（2）, γ = 72.248（2）°, V= 1109.4（3） A3, Z = 2, ρcaloa = 1.342 g/cm3, the final R= 0.0342 for 4817 observed reflections with I 〉 2σ（I） and Rw = 0.1263 for all data. C6H16N204 （II）： space group P1, a = 5.5513（10）, b = 5.5589（11）, c = 7.4437（14） A, α = 94.332（4）, β = 104.497（4）, γ = 103.487（4）°,V= 214.06（7） A3, Z = 1, ρcalcd = 1.398 g/cm3, the final R = 0.0431 for 829 observed reflections with I〉 2σ（I） and Rw = 0.1263 for all data. C14H37CuN40 （III）, space group P21/n, a = 9.050（9）, b = 18.434（17）, c = 11.659（11） A, β = 107.134（19）°, V= 1859（3） A3, Z = 4, ρcalcd =1.443 g/cm3, the final R = 0.0616 for 3308 observed reflections （O 〉 2σ（I）） and Rw = 0.1229 for all data. Their structures were all determined by X-ray diffraction, elemental analysis and IR.
文摘Adsorption of Cu(II) and Co(II) from aqueous solutions on synthetic nano Fe3O4 has been studied. The effect of experimental parameters such as initial concentration of the metal ions, adsorbent dosage, contact time and pH has been investigated. Optimum removal efficiency of Cu(II) ion was found to be 97.8% with the dose rate of 1.07 g/L in 60 minutes at pH = 5.5 and for Co(II) ion, it was found to be 99.2% with the dose rate of2.57 g/L in 10 minutes at pH = 5.4. The removal of Co(II) ions require only 10 minutes with the efficient removal of 99.2%, whereas Cu(II) ions require 60 minutes with the maximum removal of 97.8%. In order to understand the effective removal of Cu(II) and Co(II) ions on Fe3O4, room temperature magnetic measurement was carried out using Vibrational Spectrum Magnetometer (VSM), before and after adsorption with a maximum applied magnetic field of 20,000 G.
文摘Cobalt and copper recovery from aqueous Co （II） and Cu（II） is one critical step for cobalt and copper wastewaters treatment. Previous tests have primarily examined Cu（II） and Co（II） removal in microbial electro- lysis cells （MECs） with abiotic cathodes and driven by microbial fuel cell （MFCs）. However, Cu（II） and Co（II） removal rates were still slow. Here we report MECs with biocathodes and driven by MFCs where enhanced removal rates of 6.0＋0.2mg·L^-1·h^-1 for Cu（II） at an initial concentration of 50 mg·L^-1 and 5.3~0.4mg·L^-1·h^-1 for Co（II） at an initial 40 mg· L^-1 were achieved, 1.7 times and 3.3 times as high as those in MECs with abiotic cathodes and driven by MFCs. Species of Cu（II） was reduced to pure copper on the cathodes of MFCs whereas Co（II） was removed associated with microorganisms on the cathodes of the connected MECs. Higher Cu（II） concentrations and smaller working volumes in the cathode chambers of MFCs further improved removal rates of Cu（II） （115.7 mg·L^-1·h^-1） and Co（II） （6.4 mg·L^-1·h^-1） with concomi- tantly achieving hydrogen generation （0.054-0.00 mol·mol^-1 COD）. Phylogenetic analysis on the bio- cathodes indicates Proteobacteria dominantly accounted for 67.9% of the total reads, followed by Firmicutes （14.0%）, Bacteroidetes （6.1%）, Tenericutes （2.5%）, Lentisphaerae （1.4%）, and Synergistetes （1.0%）. This study provides a beneficial attempt to achieve simultaneous enhanced Cu（II） and Co（II） removal, and efficient Cu（II） and Co（II） wastewaters treatment without any external energy consumption.
文摘Two three-dimensional supramolecular water architectures,[Zn(phen)3]2 ·[Zn(C10H16O4)·(H2O)3]·(C10H16O4)2·20H2O(1) and [Co(phen)3]2 ·[Co(H2O)6]·(C10H16O4)3·30H2O(2)[phen=1,10-Phenanthroline,C10H16O4=sebacic dianion],have been synthesized and characterized by IR,elemental analysis,thermogravimetric analysis,and single-crystal X-ray diffractions.The two structures both contain extensive hydrogen bonding between water molecules as well as between water molecules and sebacic anions.The water molecules and sebacic acid O atoms assembled 2D supramolecular corrugated sheets with different morphology in the two complexes.
基金Supported by the National Natural Science Foundation of China (No. 20773057)Liaoning Provincial Educational Commission (No. 605L207)
文摘Two new one-dimensional chain-like coordination polymers,[Cu（H2O）（dpa）- MoO4]·H2O 1 and [Co（H2O）（dpa）MoO4] 2,have been synthesized under hydrothermal reactions. Their structures were determined by single-crystal X-ray diffraction analysis. Crystal data for 1： [Cu（H2O）（dpa）MoO4]·H2O,Mr = 430.71,monoclinic,space group P21/c,a = 9.5469（10）,b = 16.6874（17）,c = 9.0799（10）A,β = 104.9100（10）°,V = 1397.8（3）A^3,Z = 4,Dc = 2.047 g/cm^3,F（000） = 852,μ = 2.449 mm-1,the final R = 0.0293 and wR = 0.0638 for 2472 independent reflections （Rint = 0.0338） and 2034 observed reflections with I 〉 2σ（I）. Crystal data for 2： [Co- （H2O）（dpa）MoO4],Mr = 408.09,monoclinic,space group P21/c,a = 10.204（2）,b = 18.933（4）,c = 6.8875（16）A,β = 102.195（3）o,Z = 4,V = 1300.5（5）A^3,Z = 4,Dc = 2.084 g/cm3,F（000） = 804,μ = 2.262 mm-1,the final R = 0.0357 and wR = 0.0693 for 3022 independent reflections （Rint = 0.0436） and 2286 observed reflections （I 〉 2σ（I））. Polymer 1 is based on a one-dimensional zigzag chain built up from {Cu（H2O）（dpa）}2＋ units bridged through the bidentate {MoO4}2- ligands. The chains extending along the c-axis are arranged alternately with two opposite orientations along the b-axis. The adjacent chains are stably packed together through π-π interactions and exhibit an interesting three-dimensional supramolecular architecture via hydrogen bonding interactions. Polymer 2 based on a one-dimensional zonal chain is built up from {Co（H2O）（dpa）}2＋ units linked by the tridentate {MoO4}2- ligands. The ribbons extend along the c-axis. In the bc layers,there are significant interactions of N-H…O-Mo hydrogen bonds and π-π overlaps of dpa ligands between adjacent ribbons.
文摘The reaction of bis-[2-amino-4-pheny1-5-thiazolyl] disulfide with 5-nitro-salicylaldehyde in absolute ethanol resulted in the formation of a new Schiff base ligand H<sub>2</sub>L (1). Characterization of the ligand was performed by FT-IR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, UV-Vis, elemental analysis and single crystal X-ray diffraction. The ligand, (1), possesses a disulfide –S–S– bridge of 2.1121 (3) ? length, and the molecule adopts a cis-conformation around this bond. In the crystal structure of (1), an intramolecular O–H···N hydrogen bond with D… A distance of 2.69 (3) ? was present. The reaction of (1) with Co(NO<sub>3</sub>)<sub>2</sub>·6H<sub>2</sub>O and CuCl<sub>2</sub>·2H<sub>2</sub>O in methanol afforded the corresponding metal complexes. The obtained solids were further investigated by elemental analysis and UV-Vis titration that confirmed the formation of [CoL] and [ClCuHL] complexes. However, recrystallizaion of the Co(II) complex in dimethylsulfoxide caused the complete hydrolysis of the imine bond and afforded a Co(II) complex in which two 5-nitro-salicylaldehyde and two DMSO molecules were coordinated to the central metal in an octahedral fashion. This structure (2) was also confirmed by single crystal X-ray analysis.
文摘A novel chemiluminescence (CL) sensor for H2O2 combined with flow injection analysis is described in this paper. H2O2 is sensed by the CL reaction with luminol and Co2+ bleeding from the ion exchange column with immobilized reagents by hydrolysis. The calibration graph is linear and falls between the range of 4x10(-8) to 1x10(-5) mol/L. A complete analysis could be performed in 1 min. The system was reused for over 50 hours.
基金Supported by the Science and Technology Foundation of Ministry of Development of China (2010-K6-8)Science Foundation of Suzhou University of Science and Technology
文摘The cobalt（II） complex with （quinolin-8-yloxy）acetate, [CoCl（C11H8NO3）]n （1）, has been prepared via the solvothermal method and characterized by IR, elemental analysis, UV- Vis diffuse-reflection spectra and single-crystal X-ray diffraction analysis. Complex 1 is a novel carboxylate-bridged one-dimensional helical cobalt（II） polymer, and the Co（II） centre exhibits an approximately square pyramidal CoClNO3 coordination geometry. It crystallizes in monoclinic, space group P21/n, with a = 9.1594（10）, b = 6.8864（7）, c = 17.290（2） , β = 102.629（3）o, C11H8ClCoNO3, Mr = 296.56, V = 1064.2（2） 3, Z = 4, Dc = 1.851 g/cm3, F（000） = 596, μ = 1.856 mm-1, the final R = 0.0308 and wR = 0.0807. Interestingly, the chain complexes are assembled to form two-dimensional networks through intermolecular face-to-face π-π stacking interactions with the centroid-to-centroid distance of 3.559（1） and the dihedral angle of 8.4（1）° between the aromatic rings.
基金supported by the National Natural Science Foundation of China(No.51278055)the National Science and Technology Major Project(No.2012ZX07203-003)
文摘A study on the removal of Co（Ⅱ） from aqueous solutions by water treatment residuals（WTR） was conducted in batch conditions. The sorption process of Co（Ⅱ） followed pseudosecondorder kinetics, with 30 hr required to reach equilibrium. Using the Langmuir adsorption isotherm model, a relatively high maximum sorption capacity of 17.31 mg/g Co（Ⅱ） was determined. The adsorption of Co（Ⅱ） was dependent on pH values and was affected by the ionic strength. Results show that Co（Ⅱ） adsorption was a spontaneous endothermic process and was favorable at high temperature. Most of the adsorbed Co（Ⅱ） stayed on the WTR permanently, whereas only small amounts of adsorbed Co（Ⅱ） were desorbed. The shifting of peaks in FT-IR spectra indicated that Co（Ⅱ） interacted with the WTR surface through strong covalent bond formation with Fe（Al）–O functional groups. It was concluded that WTR can be a suitable material from which to develop an efficient adsorbent for the removal of Co（Ⅱ） from wastewater.
