A new coordination polymer, [Mn（L）（1,4-bdc）] （L = 11-fluoro-dipyrido[3,2- a：2＂,3 ＂- c]phenazine, 1,4-bdc - benzene-1,4-dicarboxylate）, has been synthesized through the hydrothermal method and characterized by...A new coordination polymer, [Mn（L）（1,4-bdc）] （L = 11-fluoro-dipyrido[3,2- a：2＂,3 ＂- c]phenazine, 1,4-bdc - benzene-1,4-dicarboxylate）, has been synthesized through the hydrothermal method and characterized by elemental analysis, IR and single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 9.7544（9）, b = 10.8254（10）, c = 11.5288（10） A, a = 114.1300（10）, β = 96.6110（10）, y = 105.0390（10）°, V= 1038.62（16）/k3, Z= 2, C26H13FMnN404, Mr = 519.34, Dc = 1.661 g/cm3, F（000） = 526, ,u（MoKa） = 0.691 mm^-, R = 0.0405 and wR = 0.0977. The 1,4-bdc dianions link the neighboring Mn（II） atoms to yield a two-dimensional layer structure. The L ligands are attached on both sides of the layer. The π-π interactions between the L ligands of neighboring layers result in a three-dimensional supramolecular architecture.展开更多
A one-dimensional double-chain coordination polymer [Mn(phen)(tsgluo)] was synthesized in a mixed solution and its crystal structure was determined by X-ray diffraction method. It crystallizes in orthorhombic system w...A one-dimensional double-chain coordination polymer [Mn(phen)(tsgluo)] was synthesized in a mixed solution and its crystal structure was determined by X-ray diffraction method. It crystallizes in orthorhombic system with space group P212121. The crystal data are: a=0.530 78(17) nm, b=1.723 9(5) nm, c=2.456 9(8) nm, Z=4, μ=0.729 mm-1, Dc=1.579 g·cm-3, V=2.248 1(12) nm3, R1=0.033 1, ωR2=0.078 9. In the title complex, each Mn(Ⅱ) ion presents a octahedral geometry with the coordination of two nitrogen atoms from 1,10-phenanthroline and four oxygen atoms from three different tsgluo2- ligands. The γ-carboxyl coordinates to Mn(Ⅱ) in the mode of bidentate chelate, while the α-carboxyl coordinates in a bidentate bridging mode. CCDC: 253910.展开更多
The title complex, [Mn（DPPZ）（PZDC）（H2O）] 1 （DPPZ = dipyrido[3,2 -a：2＇,3＇- c]phenazine and H2PZDC = pyrazine-2,3-dicarboxylic acid）, has been hydrothermally synthesized and structurally characterized by X-ra...The title complex, [Mn（DPPZ）（PZDC）（H2O）] 1 （DPPZ = dipyrido[3,2 -a：2＇,3＇- c]phenazine and H2PZDC = pyrazine-2,3-dicarboxylic acid）, has been hydrothermally synthesized and structurally characterized by X-ray single-crystal diffraction, elemental analyses, IR, TG- DTA and magnetic susceptibility measurement. It crystallizes in triclinic, space group P1^- with a = 6.6842（5）, b = 7.5741（6）, c = 20.5755（15）A, α = 90.1160（10）, β = 97.0560（10）, γ = 97.3350（10）°, V= 1025.16（13）A^3, Z = 2, MnC24H14N6O5, Mr= 521.35, Dc= 1.689 g/cm^3, F（000） = 530, μ（MoKa） = 0.699 mm^-1, R = 0.0366 and wR = 0.0810. Compound 1 contains one- dimensional chains which are further stacked through π-π interactions to form a 3D supramolecular architecture. The water molecule O（1W） is involved in hydrogen bonding interactions with symmetric carboxylate oxygen atom 0（4） at （x＋ 1, y＋1, z） and symmetric PZDC nitrogen atom N（6） at （1-x, 1-y, 1-z）, which completes the structure of 1. Magnetic susceptibility measurement indicates that the compound behaves a weak antiferromagnetic exchange interaction.展开更多
The key role of manganese(Mn)in the biogeochemical cycle of trace elements has been of great interest in recent years.Nevertheless,the redox properties of aqueous Mn(Ⅲ)have been studied to a lesser extent.Mn(Ⅲ)is no...The key role of manganese(Mn)in the biogeochemical cycle of trace elements has been of great interest in recent years.Nevertheless,the redox properties of aqueous Mn(Ⅲ)have been studied to a lesser extent.Mn(Ⅲ)is not stable in solution by itself.However,when complexed with inorganic ligands,it has shown potential to oxidize and reduce trace elements.In the present study,we are exploring the redox characteristics of the complex Mn(Ⅲ)-Pyrophosphate(Mn(Ⅲ)-PP).This complex is stable over a wide range of pH values but requires the ratio of Mn:PP to be less than 1:6.Specifically,the redox reaction of chromium(Cr(Ⅲ))and Mn(Ⅲ)-PP is investigated.A solid,Cr(OH)_(3),is used as a source of Cr(Ⅲ).For this reaction,environmentally relevant parameters,such as pH,ionic strength,ratio Mn(Ⅲ)/Cr(Ⅲ),and excess of ligand,were assessed.Results showed that Mn(Ⅲ)can effectively oxidize Cr(Ⅲ)to Cr(Ⅵ),taking about 15 days for the reaction to complete.This reaction occurs only under acidic conditions(pH4),and with a low excess of Pyrophosphate.The initial Mn(Ⅲ)concentration decreases as the Cr(Ⅵ)is produced,and Cr(Ⅵ)can be adsorbed back into the Cr(OH)_(3)surface,limiting the mobility of this toxic species.Despite this adsorption,significant amounts of Cr(VI)are release in the aqueous phase.This study shows the importance of a mobile species(Mn-PP complex)in the oxidation of Cr(Ⅲ)and the release of Cr(Ⅵ)to the environment.展开更多
A mononuclear manganese complex [Mn(2,2′-bipy)(H2O)4]·(m-phth) (2,2′-bipy=2,2′-bipyridine, m-phth=isophthalate) has been synthesized by hydrothermal methods. The crystal structure was determined by single-crys...A mononuclear manganese complex [Mn(2,2′-bipy)(H2O)4]·(m-phth) (2,2′-bipy=2,2′-bipyridine, m-phth=isophthalate) has been synthesized by hydrothermal methods. The crystal structure was determined by single-crystal X-ray diffraction. The crystal is of orthorhombic, space group Pnna with a=0.766 8(8) nm, b=2.050 2(2) nm, c=1.247 0(13) nm, V=1.960 4(4) nm3, Z=4, Mr=447.30, Dc=1.376 g·cm-3, μ=0.722 mm-1, F(000)=924, Rint=0.027 0, R=0.028 0 and wR=0.075 5. In the crystal the manganese atom is six-coordinated by two nitrogen atoms from 2,2′-bipyradine and four oxygen atoms from water molecules, completing an octahedral coordination geometry. The isophthalate molecules are included in the lattice and connected to Mn(2,2′-bipy)(H2O)4 by hydrogen bonding interactions to form a three-dimensional supramolecular structure. CCDC:286965.展开更多
Five manganese complexes of Schiff b ase were synthesized:[Mn Ⅳ,Ⅳ (μ-O)(Salen)] 2 ·DMF ·H 2 O(1),[Mn Ⅳ,Ⅳ (μ-O)(5-BrSalen)] 2 ·DMF ·0.5H 2 O(2),[Mn Ⅳ,Ⅳ (μ-O)]al(1,2-pn)[nr 2 ·H 2 O(3),...Five manganese complexes of Schiff b ase were synthesized:[Mn Ⅳ,Ⅳ (μ-O)(Salen)] 2 ·DMF ·H 2 O(1),[Mn Ⅳ,Ⅳ (μ-O)(5-BrSalen)] 2 ·DMF ·0.5H 2 O(2),[Mn Ⅳ,Ⅳ (μ-O)]al(1,2-pn)[nr 2 ·H 2 O(3),]Mn Ⅳ,Ⅳ (μ-O)[5-Br-Sal(1,2-pn)]r 2 ·H 2 O(4),[Mn Ⅳ,Ⅳ (μ-O)]5-CH 3 -Sal(1,2-pn)5-CH 3 -Sal(1,2-pn)[ 2 ·2H 2 O(5),and were characterized by element analysis,IR and UV-Vis spec tra.The results of cyclic voltammogram show that Schiff base ligands can drop the potential of manganese and s teady high oxide state of manganese.The magnetic properties of1and3have also been studied.The results show t hat there is a weak ferromagneticall y coupling of Mn Ⅳ2 pair at room and low temperature,and the interactions o f complex3are weaker than complex1.展开更多
基金Supported by the Institute Foundation of Siping City (No.2009011)
文摘A new coordination polymer, [Mn（L）（1,4-bdc）] （L = 11-fluoro-dipyrido[3,2- a：2＂,3 ＂- c]phenazine, 1,4-bdc - benzene-1,4-dicarboxylate）, has been synthesized through the hydrothermal method and characterized by elemental analysis, IR and single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 9.7544（9）, b = 10.8254（10）, c = 11.5288（10） A, a = 114.1300（10）, β = 96.6110（10）, y = 105.0390（10）°, V= 1038.62（16）/k3, Z= 2, C26H13FMnN404, Mr = 519.34, Dc = 1.661 g/cm3, F（000） = 526, ,u（MoKa） = 0.691 mm^-, R = 0.0405 and wR = 0.0977. The 1,4-bdc dianions link the neighboring Mn（II） atoms to yield a two-dimensional layer structure. The L ligands are attached on both sides of the layer. The π-π interactions between the L ligands of neighboring layers result in a three-dimensional supramolecular architecture.
文摘A one-dimensional double-chain coordination polymer [Mn(phen)(tsgluo)] was synthesized in a mixed solution and its crystal structure was determined by X-ray diffraction method. It crystallizes in orthorhombic system with space group P212121. The crystal data are: a=0.530 78(17) nm, b=1.723 9(5) nm, c=2.456 9(8) nm, Z=4, μ=0.729 mm-1, Dc=1.579 g·cm-3, V=2.248 1(12) nm3, R1=0.033 1, ωR2=0.078 9. In the title complex, each Mn(Ⅱ) ion presents a octahedral geometry with the coordination of two nitrogen atoms from 1,10-phenanthroline and four oxygen atoms from three different tsgluo2- ligands. The γ-carboxyl coordinates to Mn(Ⅱ) in the mode of bidentate chelate, while the α-carboxyl coordinates in a bidentate bridging mode. CCDC: 253910.
基金The project was supported by the Natural Science Foundation of Jilin Province (No. 20060516)the Doctoral Foundation of Jilin Normal University (No. 2006006)+1 种基金the Science and Technology Institute Foundation of Siping City (No. 2005016)the Subject and Base Construction Foundation of Jilin Normal University (No. 2006041)
文摘The title complex, [Mn（DPPZ）（PZDC）（H2O）] 1 （DPPZ = dipyrido[3,2 -a：2＇,3＇- c]phenazine and H2PZDC = pyrazine-2,3-dicarboxylic acid）, has been hydrothermally synthesized and structurally characterized by X-ray single-crystal diffraction, elemental analyses, IR, TG- DTA and magnetic susceptibility measurement. It crystallizes in triclinic, space group P1^- with a = 6.6842（5）, b = 7.5741（6）, c = 20.5755（15）A, α = 90.1160（10）, β = 97.0560（10）, γ = 97.3350（10）°, V= 1025.16（13）A^3, Z = 2, MnC24H14N6O5, Mr= 521.35, Dc= 1.689 g/cm^3, F（000） = 530, μ（MoKa） = 0.699 mm^-1, R = 0.0366 and wR = 0.0810. Compound 1 contains one- dimensional chains which are further stacked through π-π interactions to form a 3D supramolecular architecture. The water molecule O（1W） is involved in hydrogen bonding interactions with symmetric carboxylate oxygen atom 0（4） at （x＋ 1, y＋1, z） and symmetric PZDC nitrogen atom N（6） at （1-x, 1-y, 1-z）, which completes the structure of 1. Magnetic susceptibility measurement indicates that the compound behaves a weak antiferromagnetic exchange interaction.
基金Nuclear Regulatory Commission(NRC)for the funds provided under award 31310019M0010。
文摘The key role of manganese(Mn)in the biogeochemical cycle of trace elements has been of great interest in recent years.Nevertheless,the redox properties of aqueous Mn(Ⅲ)have been studied to a lesser extent.Mn(Ⅲ)is not stable in solution by itself.However,when complexed with inorganic ligands,it has shown potential to oxidize and reduce trace elements.In the present study,we are exploring the redox characteristics of the complex Mn(Ⅲ)-Pyrophosphate(Mn(Ⅲ)-PP).This complex is stable over a wide range of pH values but requires the ratio of Mn:PP to be less than 1:6.Specifically,the redox reaction of chromium(Cr(Ⅲ))and Mn(Ⅲ)-PP is investigated.A solid,Cr(OH)_(3),is used as a source of Cr(Ⅲ).For this reaction,environmentally relevant parameters,such as pH,ionic strength,ratio Mn(Ⅲ)/Cr(Ⅲ),and excess of ligand,were assessed.Results showed that Mn(Ⅲ)can effectively oxidize Cr(Ⅲ)to Cr(Ⅵ),taking about 15 days for the reaction to complete.This reaction occurs only under acidic conditions(pH4),and with a low excess of Pyrophosphate.The initial Mn(Ⅲ)concentration decreases as the Cr(Ⅵ)is produced,and Cr(Ⅵ)can be adsorbed back into the Cr(OH)_(3)surface,limiting the mobility of this toxic species.Despite this adsorption,significant amounts of Cr(VI)are release in the aqueous phase.This study shows the importance of a mobile species(Mn-PP complex)in the oxidation of Cr(Ⅲ)and the release of Cr(Ⅵ)to the environment.
文摘A mononuclear manganese complex [Mn(2,2′-bipy)(H2O)4]·(m-phth) (2,2′-bipy=2,2′-bipyridine, m-phth=isophthalate) has been synthesized by hydrothermal methods. The crystal structure was determined by single-crystal X-ray diffraction. The crystal is of orthorhombic, space group Pnna with a=0.766 8(8) nm, b=2.050 2(2) nm, c=1.247 0(13) nm, V=1.960 4(4) nm3, Z=4, Mr=447.30, Dc=1.376 g·cm-3, μ=0.722 mm-1, F(000)=924, Rint=0.027 0, R=0.028 0 and wR=0.075 5. In the crystal the manganese atom is six-coordinated by two nitrogen atoms from 2,2′-bipyradine and four oxygen atoms from water molecules, completing an octahedral coordination geometry. The isophthalate molecules are included in the lattice and connected to Mn(2,2′-bipy)(H2O)4 by hydrogen bonding interactions to form a three-dimensional supramolecular structure. CCDC:286965.
文摘Five manganese complexes of Schiff b ase were synthesized:[Mn Ⅳ,Ⅳ (μ-O)(Salen)] 2 ·DMF ·H 2 O(1),[Mn Ⅳ,Ⅳ (μ-O)(5-BrSalen)] 2 ·DMF ·0.5H 2 O(2),[Mn Ⅳ,Ⅳ (μ-O)]al(1,2-pn)[nr 2 ·H 2 O(3),]Mn Ⅳ,Ⅳ (μ-O)[5-Br-Sal(1,2-pn)]r 2 ·H 2 O(4),[Mn Ⅳ,Ⅳ (μ-O)]5-CH 3 -Sal(1,2-pn)5-CH 3 -Sal(1,2-pn)[ 2 ·2H 2 O(5),and were characterized by element analysis,IR and UV-Vis spec tra.The results of cyclic voltammogram show that Schiff base ligands can drop the potential of manganese and s teady high oxide state of manganese.The magnetic properties of1and3have also been studied.The results show t hat there is a weak ferromagneticall y coupling of Mn Ⅳ2 pair at room and low temperature,and the interactions o f complex3are weaker than complex1.
