A new cobalt（II） complex [Co（NO2-salen）2]·1.5H2O containing mono acetalization Schiff base ligand（NO2-salen = N-5-nitro-salicylideneamino ethanato） has been prepared through one-pot template condensation, a...A new cobalt（II） complex [Co（NO2-salen）2]·1.5H2O containing mono acetalization Schiff base ligand（NO2-salen = N-5-nitro-salicylideneamino ethanato） has been prepared through one-pot template condensation, and has been structurally characterized by elemental analysis, IR spectra and X-ray diffraction. It is formulated as C18H23CoN6O7.5, crystallizes in the hexagonal system, space group of R-3c with α = 25.895（18）, b = 25.895（18）, c = 35.075（6）, γ = 120o, V = 20368（3） and Z = 36. The ligand of 5-nitrosalicylaldehyde-ethylene-diamine takes unusual mono asymmetry mode. The Co（II） ion exhibits a coordination number of six, and assumes a distorted octahedral geometry with a N2O4 donor set. The neutral monomeric units of [Co（NO2-salen）2]·1.5H2O are linked into a one-dimensional（1D） structure via the intermolecular hydrogen bonds and weak π-π stacking interactions. Cyclic-voltammetry measurement reveals the oxidation and reduction processes for the complex are irreversible in nature.展开更多
Reaction of 3,5-pyridine-dicarboxylic acid（3,5-PydcH2） with iron salt in hydrothermal condition results in the formation of a three-dimensional self-assembly network formulated as [C14H14Fe2N2O12]n,and it has been s...Reaction of 3,5-pyridine-dicarboxylic acid（3,5-PydcH2） with iron salt in hydrothermal condition results in the formation of a three-dimensional self-assembly network formulated as [C14H14Fe2N2O12]n,and it has been structurally characterized by elemental analysis,IR spectra and X-ray diffraction.It crystallizes in the monoclinic system,space group C2/c with a=9.9633（15）,b=12.0942（18）,c=7.4297（11）A and β=105.822o.The units of Fe2（pydc）2·2H2O are linked into a one-dimensional structure via the chelate carboxylate groups from the 3,5-pyridine-dicarboxylate.The interlayer hydrogen bonding interactions result in a three-dimensional supramolecular architecture.In the complex,the Fe（Ⅲ） ion displays a slightly distorted pentagonal bipyramidal geometry with seven coordination numbers.Cyclic-voltammetry measurement reveals the oxidation and reduction processes for the complex are quasi-reversible in nature.展开更多
The divalent state of Ln（III） ions has attracted much interest because of their ability to serve isomorphously in many biological system of divalent Ca（II） ion. Therefore, present paper deals with the study of div...The divalent state of Ln（III） ions has attracted much interest because of their ability to serve isomorphously in many biological system of divalent Ca（II） ion. Therefore, present paper deals with the study of divalent state of Eu（III） and Nd（III） ions in non-aqueous medium. In present study, cyclic voltammetry and chronopotentiometry were utilized to establish the divalent state of Eu（III） and Nd（III） ions. The cyclic voltammetric technique showed two-step reduction process at cathode for both Ln（III） ions under specified experimental conditions and chronopotentiometric method also showed two different transition times （r）. Looking to the shape of cyclic voltammogram we calculated het- erogeneous forward rate constant （K^fh, cm/s） and diffusion coefficient （D, cm2/s） for both ions, which suggested that sweep rate had great ef- fect on the shape of cyclic voltammogram of Eu（III） and Nd（III） ions. The result of chronopotentiometry also suggested that stable divalent states of Eu（III） and Nd（III） ions existed with chronopotentiogram with two distinct transition times. The diffusion coefficients （D, cm2/s） were calculated from Sand equation. The diffusion coefficients of both techniques were compared and the results suggested that the system at electrode surface was changing from being reversible to irreversible.展开更多
基金supported by the National Natural Science Foundation of China(No.21273101)the Foundation of the Program for Backbone Teachers in Universities of Henan Province(No.2012GGJS158)+1 种基金tackle key problem of science and technology Project of Henan Province(No.142102310483)the Foundation of Education Committee of Henan Province(No.14B150033)
文摘A new cobalt（II） complex [Co（NO2-salen）2]·1.5H2O containing mono acetalization Schiff base ligand（NO2-salen = N-5-nitro-salicylideneamino ethanato） has been prepared through one-pot template condensation, and has been structurally characterized by elemental analysis, IR spectra and X-ray diffraction. It is formulated as C18H23CoN6O7.5, crystallizes in the hexagonal system, space group of R-3c with α = 25.895（18）, b = 25.895（18）, c = 35.075（6）, γ = 120o, V = 20368（3） and Z = 36. The ligand of 5-nitrosalicylaldehyde-ethylene-diamine takes unusual mono asymmetry mode. The Co（II） ion exhibits a coordination number of six, and assumes a distorted octahedral geometry with a N2O4 donor set. The neutral monomeric units of [Co（NO2-salen）2]·1.5H2O are linked into a one-dimensional（1D） structure via the intermolecular hydrogen bonds and weak π-π stacking interactions. Cyclic-voltammetry measurement reveals the oxidation and reduction processes for the complex are irreversible in nature.
基金supported by the National Natural Science Foundation of China (Nos 20771054 and 20671076)the Natural Science Foundation of Henan Province (No 0311021200)
文摘Reaction of 3,5-pyridine-dicarboxylic acid（3,5-PydcH2） with iron salt in hydrothermal condition results in the formation of a three-dimensional self-assembly network formulated as [C14H14Fe2N2O12]n,and it has been structurally characterized by elemental analysis,IR spectra and X-ray diffraction.It crystallizes in the monoclinic system,space group C2/c with a=9.9633（15）,b=12.0942（18）,c=7.4297（11）A and β=105.822o.The units of Fe2（pydc）2·2H2O are linked into a one-dimensional structure via the chelate carboxylate groups from the 3,5-pyridine-dicarboxylate.The interlayer hydrogen bonding interactions result in a three-dimensional supramolecular architecture.In the complex,the Fe（Ⅲ） ion displays a slightly distorted pentagonal bipyramidal geometry with seven coordination numbers.Cyclic-voltammetry measurement reveals the oxidation and reduction processes for the complex are quasi-reversible in nature.
文摘The divalent state of Ln（III） ions has attracted much interest because of their ability to serve isomorphously in many biological system of divalent Ca（II） ion. Therefore, present paper deals with the study of divalent state of Eu（III） and Nd（III） ions in non-aqueous medium. In present study, cyclic voltammetry and chronopotentiometry were utilized to establish the divalent state of Eu（III） and Nd（III） ions. The cyclic voltammetric technique showed two-step reduction process at cathode for both Ln（III） ions under specified experimental conditions and chronopotentiometric method also showed two different transition times （r）. Looking to the shape of cyclic voltammogram we calculated het- erogeneous forward rate constant （K^fh, cm/s） and diffusion coefficient （D, cm2/s） for both ions, which suggested that sweep rate had great ef- fect on the shape of cyclic voltammogram of Eu（III） and Nd（III） ions. The result of chronopotentiometry also suggested that stable divalent states of Eu（III） and Nd（III） ions existed with chronopotentiogram with two distinct transition times. The diffusion coefficients （D, cm2/s） were calculated from Sand equation. The diffusion coefficients of both techniques were compared and the results suggested that the system at electrode surface was changing from being reversible to irreversible.
