A novel two-dimensional supramolecular complex [Mn(phen)(DPZDA)(H2O)]·2H2O has been synthesized by the reaction of Mn(CH3COO)2, 1,10-phenanthroline (phen) and H2DPZDA (3,5-dimethyl-pyrazine-2,6-dicarbo...A novel two-dimensional supramolecular complex [Mn(phen)(DPZDA)(H2O)]·2H2O has been synthesized by the reaction of Mn(CH3COO)2, 1,10-phenanthroline (phen) and H2DPZDA (3,5-dimethyl-pyrazine-2,6-dicarboxylic acid). Elemental analysis, IR spectra and X-ray singlecrystal diffraction were carried out to determine the composition and crystal structure of the title complex. Crystal data: triclinic system, space group P1, a = 7.7474(13), b = 9.3381(15), c = 15.146(3) A, α = 93.872(3), β= 102.451 (11 ), y = 105.261 ( 11)°, C20H20MnN4O7, Mr = 483.34, Z = 2, F(000) = 498, V=1023.2(3)A^3, Dc=1.569 g/cm^3,μ=0.697 mm^-1, -9≤h≤9, -11≤k≤10, -18≤l≤12, R = 0.0365 and wR=0.0901 for 3585 independent reflections (Rint= 0.0165) and 2923 observed reflections (I〉 2σ(I)). Structural analysis indicates that Mn(Ⅱ) adopts a distorted octahedral geometry. The 2-D framework supramolecular structure of the title complex is constructed from hydrogen bonds and π…π interactions.展开更多
A new one-dimensional Mn(Ⅱ) complex, [MnL2(bipy)(H2O)2]n 1, has been obtained by the reaction of MnCl2·4H2O, 2,2'-bipyridine (bipy) and 1-(4-phenoxyacetate)-5-thioacetatetetrazole (H2L). The crystal...A new one-dimensional Mn(Ⅱ) complex, [MnL2(bipy)(H2O)2]n 1, has been obtained by the reaction of MnCl2·4H2O, 2,2'-bipyridine (bipy) and 1-(4-phenoxyacetate)-5-thioacetatetetrazole (H2L). The crystal crystallizes in the triclinic system, space group Pi with a = 7.6088(2), b = 12.2795(2), c = 13.6617(3)A, α = 75.416(2), β =79.264(2), γ = 74.271(2)°, V = 1179.48(4) A3, Z = 2, Mr = 555.43, F(000) = 570, Dc = 1.564 g/cm^3, μ = 0.704 mm^-1, the final R = 0.0454 and wR = 0.0849 for 3127 observed reflections (Ⅰ〉 2σ(Ⅰ)). The Mn(Ⅱ) is six-coordinated by two water molecules, two N atoms from bipy and two carboxylate O atoms from two L^2- to form a distorted octahedral geometry. Each L^2- ligand serves as a bridging ligand to link two Mn(Ⅱ) atoms, leading to a single-strand zigzag coordination polymer. Hydrogen-bonding interactions between adjacent chains as well as π-π stacking interactions extend the complex into a three-dimensional supramolecular architecture. Moreover, the title compound emits strong red fluorescent light (λem(max) = 610 nm) in EtOH solution.展开更多
The mixture of(2NaBH4+ MnCl2) was ball milled in a magneto-mill. No gas release was detected. The XRD patterns of the ball milled mixture exhibit only the Bragg diffraction peaks of the Na Cl-type salt which on the ba...The mixture of(2NaBH4+ MnCl2) was ball milled in a magneto-mill. No gas release was detected. The XRD patterns of the ball milled mixture exhibit only the Bragg diffraction peaks of the Na Cl-type salt which on the basis of the present X-ray diffraction results and the literature is likely to be a solid solution Na(Cl)x(BH4)(1-x), possessing a cubic Na Cl-type crystalline structure. No presence of any crystalline hydride was detected by powder X-ray diffraction which clearly shows that NaBH4in the initial mixture must have reacted with MnCl2forming a Na Cl-type by-product and another hydride that does not exhibit X-ray Bragg diffraction peaks. Mass spectrometry(MS) of gas released from the ball milled mixture during combined MS/thermogravimetric analysis(TGA)/differential scanning calorimetry(DSC) experiments, confirms mainly hydrogen(H2) with a small quantity of diborane gas, B2H6. The Fourier transform infra-red(FT-IR) spectrum of the ball milled(2NaBH4+ MnCl2) is quite similar to the FT-IR spectrum of crystalline manganese borohydride, c-Mn(BH4)2, synthesized by ball milling, which strongly suggests that the amorphous hydride mechano-chemically synthesized during ball milling could be an amorphous manganese borohydride. Remarkably, the process of solvent filtration and extraction at 42 °C, resulted in the transformation of mechano-chemically synthesized amorphous manganese borohydride to a nanostructured,crystalline, c-Mn(BH4)2hydride.展开更多
The crystal structure of one novel Mn(II) complex, [Mn(pmta)_3]_2[Mn(H_2O)_6]·4H_2O(1), is reported(Hpmta = 5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxylic acid). In the title compound, the asymmetric ...The crystal structure of one novel Mn(II) complex, [Mn(pmta)_3]_2[Mn(H_2O)_6]·4H_2O(1), is reported(Hpmta = 5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxylic acid). In the title compound, the asymmetric unit consists of a [Mn(pmta_)3]ˉ anion, half [Mn(H_2O)_6]^(2+) counter cation and two lattice H_2O molecules, and the intra- and intermolecular hydrogen bonds connect the complex into a supramolecular structure. The liquid-state fluorescence spectra of complex 1 have been determined. Hirshfeld surface analysis was also studied. The main intermolecular interactions in the complex are O···H and H···H contacts.展开更多
A coordination polymer [Mn2(ctpt)2(aic)2]n (1, ctpt = 2-(4-chloro-phenyl)-1H- 1,3,7,8-tetraaza-cyclopenta[l]phenanthrene, H2aic = 5-amino-isophthalic acid) was hydrother- mally designed and synthesized. The co...A coordination polymer [Mn2(ctpt)2(aic)2]n (1, ctpt = 2-(4-chloro-phenyl)-1H- 1,3,7,8-tetraaza-cyclopenta[l]phenanthrene, H2aic = 5-amino-isophthalic acid) was hydrother- mally designed and synthesized. The complex was characterized by elemental analysis, IR spectro- scopy, single-crystal X-ray diffraction, and thermogravimetric analysis (TGA). Each Mn(II) atom is linked by the aic ligands with neighbor Mn(II) atoms, forming an infinite one-dimensional (1D) double-chain structure. Complex 1 crystallizes in monoclinic, space group C2/c, with a = 18.23(1), b = 17.27(1), c = 16.69(1) ?, V = 4814.0(7) ?3, C27H16ClMnN5O4, Mr = 564.84, Dc = 1.559 g/cm3, μ(MoKα) = 0.706 mm-1, F(000) = 2296, Z = 8, the final R = 0.0487 and wR = 0.1269 (I 〉 2σ(I)). The 1D chain structure of complex 1 is stable below 458 ℃. In addition, to elucidate the essential electronic characters of this complex, theoretical calculation analysis of 1 was performed by the PBE0/LANL2DZ method in Gaussian 03 Program.展开更多
The coordination polymer [Mn2(cipt)2(aic)2]n (cipt = 2-(3-chlorophenyl)-1H- imidazo[4,5-f][1,10]phenanthroline, aic = 5-amino-isophthalic acid) has been obtained from hydrothermal reaction and characterized by...The coordination polymer [Mn2(cipt)2(aic)2]n (cipt = 2-(3-chlorophenyl)-1H- imidazo[4,5-f][1,10]phenanthroline, aic = 5-amino-isophthalic acid) has been obtained from hydrothermal reaction and characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction. The title compound crystallizes in the triclinic system, space group P , with a = 11.523(3), b = 12.162(3), c = 18.706(5) A^°, β = 81.789(5)°, V = 2455.2(1) A^°3, C54H32Cl2Mn2N10O8, Mr = 1129.68, Z = 2, Dc = 1.528 g/cm3, μ = 0.692 mm^-1, F(000) = 1148, R = 0.064 and wR = 0.145 for 9571 observed reflections (I 〉 2σ(I)). In this polymer, the Mn(II) atoms adopt different coordination modes. The Mn(1) atom is five-coordinated, forming a distorted tetragonal pyramidal geometry. Mn(2) atom is six-coordinated to get a distorted octahedral geometry, which is different from the Mn(1) atom. Each Mn(II) atom is linked by aic ligands with neighboring Mn(II) atoms, forming an infinite one-dimensional (1D) double-chain structure. The existence of N–H…O hydrogen bonding interactions leads the 1D chains to generate a 2D structure. Luminescent properties for the ligand cipt and compound 1 have also been discussed in detail.展开更多
The coordination polymer, [Mn3(bpta)2(bip)2], (H3bpta = biphenyl-3,3',5-tricar- boxylic acid, bip = 2,6-bis(imidazole-1-yl)pyridine), has been synthesized under hydrothermal con- ditions and characterized by ...The coordination polymer, [Mn3(bpta)2(bip)2], (H3bpta = biphenyl-3,3',5-tricar- boxylic acid, bip = 2,6-bis(imidazole-1-yl)pyridine), has been synthesized under hydrothermal con- ditions and characterized by elemental analysis, FT-IR, XRD, TGA and single-crystal X-ray diffraction. It crystallizes in monoclinic, space group P21/c with a = 14.919(3), b = 9.780(2), c = 20.352(7) A, V = 2344.4(10) A3, Z= 2, C52H32Mn3N10012, Mr = 1153.70, Dc = 1.634 g/cm3, p(MoKa) = 0.876 mm-1, F(000) = 1170, the finalR = 0.0605 and wR = 0.1177. The complex forms a 2D layer with trinuclear Mn(II) units and further assembles into a 3D supramolecular network structure through C-H..'O hydrogen bonding and C-H...π interactions. Moreover, the negative J value indicates the presence of antiferromagnetic coupling between the Mn(II) ions within a trinuclear unit.展开更多
One new coordination polymer, [Mn(Hbtc)(bpy)(HO)]1, was synthesized by the reaction of manganese(Ⅱ) salt under pH-controlled hydrothermal conditions with unsymmetrical polycarboxylic acid of 1,2,4-benzenetricarboxyli...One new coordination polymer, [Mn(Hbtc)(bpy)(HO)]1, was synthesized by the reaction of manganese(Ⅱ) salt under pH-controlled hydrothermal conditions with unsymmetrical polycarboxylic acid of 1,2,4-benzenetricarboxylic acid(Hbtc) and 2,2?-bipyridine(bpy). The structure of complex 1 was characterized by single-crystal X-ray diffraction, IR spectra, powder X-ray analysis, thermal gravimetric analysis(TGA), UV-Vis spectrometry, photoluminescence and magnetic susceptibility. Complex 1 is a one-dimensional(1D) polymeric single-chain structure. Photoluminescence property is quite similar to the bpy ligand. Magnetic susceptibility measurement indicates that 1 shows a weak ferromagnetic coupling between the Mn~Ⅱ ions.展开更多
The crystal structure and thermal stability of the martensite in Cu 24Al 3Mn (mole fraction, %) alloy were studied by X ray diffraction, electron diffraction, V - t curve measurement. The 18R martensite with fairly pe...The crystal structure and thermal stability of the martensite in Cu 24Al 3Mn (mole fraction, %) alloy were studied by X ray diffraction, electron diffraction, V - t curve measurement. The 18R martensite with fairly perfect long range order can be obtained by water quenching the alloy. The atoms distribution on the basal plane of the martensite is as follows: Ⅰ, 3/25 Mn+22/25 Cu; Ⅱ, 3/25 Al+22/25 Cu; Ⅲ, 18/25 Al+7/25 Cu, correspondingly, the parent phase may have Heusler structure. From the electron diffraction result, the crystal structure is determined to be of a modified 18R type but closely approaching orthorhombic 18R type, its lattice parameters are determined to be a = 0.447?4?nm, b = 0.522?9?nm, c = 3.815?nm and β =89.6° from the X ray diffraction results. The obtained alloy has a higher thermal stability than that of the conventional Cu Zn Al alloy.展开更多
A three-dimensional coordination polymer [Mn2(μ1.3-N3)4(μ-PP)2]n (PP = 3-(pyrazin-2-yloxy)-pyridine) has been synthesized with 3-(pyrazin-2-yloxy)-pyridine and azide anion as mixed bridge ligand, and its c...A three-dimensional coordination polymer [Mn2(μ1.3-N3)4(μ-PP)2]n (PP = 3-(pyrazin-2-yloxy)-pyridine) has been synthesized with 3-(pyrazin-2-yloxy)-pyridine and azide anion as mixed bridge ligand, and its crystal structure was determined by X-ray crystallography. The crystal data: triclinic system, space group P1, with a = 6.794(4), b = 9.885(6), c = 9.947(6) A, α = 64.170(6), β= 84.190(8), γ= 85.319(8)°, V = 597.7(6)A^3, Z = 1, C18H14Mn2N18O2, Mr = 624.35, Dc = 1.735 g/cm^3, F(000) = 314 and μ = 1.117 mm^-1. In the crystal, the azide anion acts as a bridge ligand and makes adjacent Mn(Ⅱ) ions connect into a two-dimensional sheet on the ab plane, then 3-(pyrazin-2-yloxy)-pyridine serves as a bidentate bridge ligand to connect neighboring sheets along展开更多
NiMnGaferromagnetic shape memory thin film was deposited onto Al foil using r.f.magnetron sputtering technique.The crystallization behavior of the film was investigated by XRD and DSC.The activation energy of crystall...NiMnGaferromagnetic shape memory thin film was deposited onto Al foil using r.f.magnetron sputtering technique.The crystallization behavior of the film was investigated by XRD and DSC.The activation energy of crystallization of the film was calculated by Kissinger’s method.The results show that the crystallization temperature of NiMnGafree-standing thin film in martensite state is 372 ℃,and the activation energy of crystallization is about 191.9 kJ·mol-1.展开更多
The step pattern of single crystal growth and the morphology at equilibrium state of(Mn, Fe)S on the wall of micro-voids in ZG25 cast steel have been observed using scanning electron microscope.The face-centred cubic(...The step pattern of single crystal growth and the morphology at equilibrium state of(Mn, Fe)S on the wall of micro-voids in ZG25 cast steel have been observed using scanning electron microscope.The face-centred cubic(Mn,Fe)S single crystal at equilibrium state is shown to be tetrakaidecahedron consisted of eight{111}planes and six{100}planes,and is a typical example of the O_h—m3m cubic crystal system.展开更多
The title compound [Mn(DPMT)2Cl2(H2O)2] (DPMT = 1-[[2-(2,4-dichlorophenyl)- 1,3-dioxolan-2-yl]methyl]-1H-1,2,4-triazole) was synthesized by the reaction of MnCl2·4H2O and DPMT in ethanol solution and its ...The title compound [Mn(DPMT)2Cl2(H2O)2] (DPMT = 1-[[2-(2,4-dichlorophenyl)- 1,3-dioxolan-2-yl]methyl]-1H-1,2,4-triazole) was synthesized by the reaction of MnCl2·4H2O and DPMT in ethanol solution and its structure was determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic, space group P21/c with a = 23.913(4), b = 7.8883(13), c = 8.6291(14)A, β = 95.816(3)°, V = 1619.4(5)A^3, Z = 2, C24H26Cl6MnN6O6, Mr = 762.15, Dc = 1.563 g/cm^3, μ = 0.950 mm^-1, S = 1.045, F(000) = 774, R = 0.0462 and wR = 0.0981. The molecular structure is a centrosymmetric conformation, and two ligands are symmetrically located on both sides of the Mn atom. The manganese atom is surrounded by two nitrogen atoms from ligands, two chlorine atoms and two oxygen atoms from water molecules to form a slightly distorted octahedral geometry.展开更多
A novel coordination polymer [Mn(bcp)(bib)0.5]n(1, H2 bcp = 1,3-bis(4-carboxyphenoxy)propane and bib = 1,4-bis(imidazol-1-yl)benzene) was synthesized under hydrothermal conditions, and was characterized by single-crys...A novel coordination polymer [Mn(bcp)(bib)0.5]n(1, H2 bcp = 1,3-bis(4-carboxyphenoxy)propane and bib = 1,4-bis(imidazol-1-yl)benzene) was synthesized under hydrothermal conditions, and was characterized by single-crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectroscopy and powder X-ray diffraction(PXRD).Complex [Mn(bcp)(bib)0.5]n(1) is of triclinic system, space group P1 with a = 7.320(5), b =11.871(5), c = 13.932(5)?,α= 111.125(5)°,β= 99.658(5)°,γ= 101.104(5)°, Z = 2, V= 1070.3(9)?3 Mr = 474.34, Dc = 1.472 g/cm^3, F(000)= 488,μ= 0.660 mm^-1, the final R = 0.0353 and wR =0.0.984 for 4373 observed reflections with I > 2σ(I). Structure analysis reveals that complex 1 displays a rare 2 D + 2 D → 2 D polyrataxane topology. Moreover, the luminescent property for 1 was investigated at room temperature.展开更多
Tricyanide building block K[Ru(ttpy)(CN)3] and [MnⅢ(salen)](ClO4) have been used to design and synthesize a heterobimetallic one-dimensional(1D) zigzag chain complex 1,[RuⅡ(ttpy)(CN)3 MnⅢ(salen)](ttpy = 4′-(p-toly...Tricyanide building block K[Ru(ttpy)(CN)3] and [MnⅢ(salen)](ClO4) have been used to design and synthesize a heterobimetallic one-dimensional(1D) zigzag chain complex 1,[RuⅡ(ttpy)(CN)3 MnⅢ(salen)](ttpy = 4′-(p-tolyl)-2,2′:6′,2″-terpyridine, salen = N,N?-ethylenebis-(salicylideneaminato)dianion). Single-crystal X-ray diffraction analysis shows complex 1 crystallizes in orthorhombic Pbca space group and the asymmetric unit of 1 contains one[-NC-RuⅡ(ttpy)(CN)(m-CN)-Mn Ⅲ-(salen)-] molecule. In the structure of 1, each [Ru Ⅱ(ttpy)(CN)3]-connects two [MnⅢ(salen)]+ with two cyanide groups in a cis-conformation, and in turn each[MnⅢ(salen)]+ unit links two [RuⅡ(ttpy)(CN)3]-building blocks in a trans-conformation, resulting in a 1D [-NC-RuⅡ-CN-MnⅢ-]n chain. Furthermore, the electronic absorption spectra and luminescence spectroscopy of complex 1 have also been studied.展开更多
A novel Mn(Ⅱ) complex Mn2(phen)2(p-MBA)4(H2O) has been hydrothermally synthesized by the reaction of p-methyl benzoic acid (p-MBA) with 1,10-phenanthroline (phen). Crystal data for this complex: monoclin...A novel Mn(Ⅱ) complex Mn2(phen)2(p-MBA)4(H2O) has been hydrothermally synthesized by the reaction of p-methyl benzoic acid (p-MBA) with 1,10-phenanthroline (phen). Crystal data for this complex: monoclinic, space group C2/c, a= 2.3328(3), b =1.5549(2), c = 1.5557(2) nm, β = 121.726(2)°, V= 4.7997(11) nm^3, Mr = 1028.85, Dc = 1.424 g/cm^3, Z = 4, F(000) = 2128, μ(MoKa) = 0.590mm^-1, GOOF = 1.060, R = 0.0333 and wR = 0.0767. In the crystal, each Mn(Ⅱ) ion is coordinated by two nitrogen atoms from one o-phenanthroline molecule, three oxygen atoms from three p-methyl benzoic acids and one oxygen atom from one water molecule, giving a six-coordinate distorted octahedral coordination geometry. Two neighboring Mn(Ⅱ) ions are bridged by two p-methyl benzoic acid groups and one water molecule, and their end positions are respectively coordinated by one 1,10-phenanthroline and one p-methyl benzoic acid molecule, giving a binuclear cage structure, of which the Mn(Ⅱ)…Mn(Ⅱ) distance is 0.3502 nm.展开更多
The 1-D chain coordination complex of {[Mn2(HCAM)3(H2bipy)]·5H2O}n (H3CAM = 4-hydroxypyridine-2,6-dicarboxylic acid, bipy = 4,4'-bipyridine) has been synthesized by the reaction of 4-hydroxypyridine-2,6-di...The 1-D chain coordination complex of {[Mn2(HCAM)3(H2bipy)]·5H2O}n (H3CAM = 4-hydroxypyridine-2,6-dicarboxylic acid, bipy = 4,4'-bipyridine) has been synthesized by the reaction of 4-hydroxypyridine-2,6-dicarboxylic acid, 4,4'-bipyridine and manganese carbonate under hydrothermal conditions, and its crystal structure was determined by X-ray diffraction method The crystal belongs to the monoclinic system, space group P21/n with a = 10.110(2), b = 20.159(4), c = 17.861(4)A,β = 99.67(3)°, V = 3.5884(12) nm3, Mr= 901.47, Z = 4, Dc= 1.669 g.cm^-3, μ= 0.798 mm^-1, F(000) = 1840, the final R = 0.0713 and ωR = 0.1853. The complex forms a 1-D chain bridged by HCAM, protonated 4,4-bipyridines link the 1-D chains to construct 2-D networks via N-H...O hydrogen bonds, and networks are further extended via π-π stacking and hydrogen bonds into 3-D supramolecular framework.展开更多
Based on a 3-(pyridine-2-yl)-4H-1,2,4-triazole ligand(Hpytr), one 2D Cd(Ⅱ) coordination polymer [Cd I(pytr)]n(1) and one 2D Mn(Ⅱ) coordination polymer [Mn(N3)(pytr)(H2O)]n(2) have been synthesize...Based on a 3-(pyridine-2-yl)-4H-1,2,4-triazole ligand(Hpytr), one 2D Cd(Ⅱ) coordination polymer [Cd I(pytr)]n(1) and one 2D Mn(Ⅱ) coordination polymer [Mn(N3)(pytr)(H2O)]n(2) have been synthesized and characterized by X-ray crystallography, elemental analysis, and fluorescence spectroscopy. 1 shows a layer coordination architecture linked by pytr ligand, and the Cd(Ⅱ) centers display slightly distorted square pyramid coordination geometries. Complex 2 shows a 2D pillared-layer coordination architecture bridged by N3-and pytr, and the Mn(Ⅱ) centers display slightly distorted octahedral geometries. The luminescent properties of 1 and the PXRD and thermal stability of complexes 1 and 2 were measured briefly.展开更多
Kinetics of oxygen adsorption on single crystal Mn<sub>5</sub>Si<sub>3</sub> (111) surface and initial surface oxidation were investigated. Oxygen chemisorbs dissociatively at room temperatur...Kinetics of oxygen adsorption on single crystal Mn<sub>5</sub>Si<sub>3</sub> (111) surface and initial surface oxidation were investigated. Oxygen chemisorbs dissociatively at room temperature on Mn and Si atoms. A fast oxidation of Si atoms occurs followed by oxidation of Mn atoms at RT. The MnO<sub>2</sub> was reduced by Si atoms and the SiO was oxidized further to SiO<sub>2</sub> during the sample heating.展开更多
基金Project supported by the Natural Science Foundation of Liaoning Province (No. 20052014) and Doctor Foundation of Shenyang Institute of Chemical Technology (No. 20063204)
文摘A novel two-dimensional supramolecular complex [Mn(phen)(DPZDA)(H2O)]·2H2O has been synthesized by the reaction of Mn(CH3COO)2, 1,10-phenanthroline (phen) and H2DPZDA (3,5-dimethyl-pyrazine-2,6-dicarboxylic acid). Elemental analysis, IR spectra and X-ray singlecrystal diffraction were carried out to determine the composition and crystal structure of the title complex. Crystal data: triclinic system, space group P1, a = 7.7474(13), b = 9.3381(15), c = 15.146(3) A, α = 93.872(3), β= 102.451 (11 ), y = 105.261 ( 11)°, C20H20MnN4O7, Mr = 483.34, Z = 2, F(000) = 498, V=1023.2(3)A^3, Dc=1.569 g/cm^3,μ=0.697 mm^-1, -9≤h≤9, -11≤k≤10, -18≤l≤12, R = 0.0365 and wR=0.0901 for 3585 independent reflections (Rint= 0.0165) and 2923 observed reflections (I〉 2σ(I)). Structural analysis indicates that Mn(Ⅱ) adopts a distorted octahedral geometry. The 2-D framework supramolecular structure of the title complex is constructed from hydrogen bonds and π…π interactions.
基金supported by the Natural Science Foundation of Zhejiang Province (No. Y406355)
文摘A new one-dimensional Mn(Ⅱ) complex, [MnL2(bipy)(H2O)2]n 1, has been obtained by the reaction of MnCl2·4H2O, 2,2'-bipyridine (bipy) and 1-(4-phenoxyacetate)-5-thioacetatetetrazole (H2L). The crystal crystallizes in the triclinic system, space group Pi with a = 7.6088(2), b = 12.2795(2), c = 13.6617(3)A, α = 75.416(2), β =79.264(2), γ = 74.271(2)°, V = 1179.48(4) A3, Z = 2, Mr = 555.43, F(000) = 570, Dc = 1.564 g/cm^3, μ = 0.704 mm^-1, the final R = 0.0454 and wR = 0.0849 for 3127 observed reflections (Ⅰ〉 2σ(Ⅰ)). The Mn(Ⅱ) is six-coordinated by two water molecules, two N atoms from bipy and two carboxylate O atoms from two L^2- to form a distorted octahedral geometry. Each L^2- ligand serves as a bridging ligand to link two Mn(Ⅱ) atoms, leading to a single-strand zigzag coordination polymer. Hydrogen-bonding interactions between adjacent chains as well as π-π stacking interactions extend the complex into a three-dimensional supramolecular architecture. Moreover, the title compound emits strong red fluorescent light (λem(max) = 610 nm) in EtOH solution.
基金supported by the Natural Sciences and Engineering Research Council of Canada (NSERC) Discovery grant to Prof. R.A. Varin
文摘The mixture of(2NaBH4+ MnCl2) was ball milled in a magneto-mill. No gas release was detected. The XRD patterns of the ball milled mixture exhibit only the Bragg diffraction peaks of the Na Cl-type salt which on the basis of the present X-ray diffraction results and the literature is likely to be a solid solution Na(Cl)x(BH4)(1-x), possessing a cubic Na Cl-type crystalline structure. No presence of any crystalline hydride was detected by powder X-ray diffraction which clearly shows that NaBH4in the initial mixture must have reacted with MnCl2forming a Na Cl-type by-product and another hydride that does not exhibit X-ray Bragg diffraction peaks. Mass spectrometry(MS) of gas released from the ball milled mixture during combined MS/thermogravimetric analysis(TGA)/differential scanning calorimetry(DSC) experiments, confirms mainly hydrogen(H2) with a small quantity of diborane gas, B2H6. The Fourier transform infra-red(FT-IR) spectrum of the ball milled(2NaBH4+ MnCl2) is quite similar to the FT-IR spectrum of crystalline manganese borohydride, c-Mn(BH4)2, synthesized by ball milling, which strongly suggests that the amorphous hydride mechano-chemically synthesized during ball milling could be an amorphous manganese borohydride. Remarkably, the process of solvent filtration and extraction at 42 °C, resulted in the transformation of mechano-chemically synthesized amorphous manganese borohydride to a nanostructured,crystalline, c-Mn(BH4)2hydride.
基金supported by the National Natural Science Foundation of China(No.20801012)New Energy Technology Co.Ltd.of Ai Naji of Jiangsu Province(No.8507040091)
文摘The crystal structure of one novel Mn(II) complex, [Mn(pmta)_3]_2[Mn(H_2O)_6]·4H_2O(1), is reported(Hpmta = 5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxylic acid). In the title compound, the asymmetric unit consists of a [Mn(pmta_)3]ˉ anion, half [Mn(H_2O)_6]^(2+) counter cation and two lattice H_2O molecules, and the intra- and intermolecular hydrogen bonds connect the complex into a supramolecular structure. The liquid-state fluorescence spectra of complex 1 have been determined. Hirshfeld surface analysis was also studied. The main intermolecular interactions in the complex are O···H and H···H contacts.
基金supported by the National Natural Science Foundation of China(No.21406085)
文摘A coordination polymer [Mn2(ctpt)2(aic)2]n (1, ctpt = 2-(4-chloro-phenyl)-1H- 1,3,7,8-tetraaza-cyclopenta[l]phenanthrene, H2aic = 5-amino-isophthalic acid) was hydrother- mally designed and synthesized. The complex was characterized by elemental analysis, IR spectro- scopy, single-crystal X-ray diffraction, and thermogravimetric analysis (TGA). Each Mn(II) atom is linked by the aic ligands with neighbor Mn(II) atoms, forming an infinite one-dimensional (1D) double-chain structure. Complex 1 crystallizes in monoclinic, space group C2/c, with a = 18.23(1), b = 17.27(1), c = 16.69(1) ?, V = 4814.0(7) ?3, C27H16ClMnN5O4, Mr = 564.84, Dc = 1.559 g/cm3, μ(MoKα) = 0.706 mm-1, F(000) = 2296, Z = 8, the final R = 0.0487 and wR = 0.1269 (I 〉 2σ(I)). The 1D chain structure of complex 1 is stable below 458 ℃. In addition, to elucidate the essential electronic characters of this complex, theoretical calculation analysis of 1 was performed by the PBE0/LANL2DZ method in Gaussian 03 Program.
基金supported by the National Natural Science Foundation of China(No.21406085)
文摘The coordination polymer [Mn2(cipt)2(aic)2]n (cipt = 2-(3-chlorophenyl)-1H- imidazo[4,5-f][1,10]phenanthroline, aic = 5-amino-isophthalic acid) has been obtained from hydrothermal reaction and characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction. The title compound crystallizes in the triclinic system, space group P , with a = 11.523(3), b = 12.162(3), c = 18.706(5) A^°, β = 81.789(5)°, V = 2455.2(1) A^°3, C54H32Cl2Mn2N10O8, Mr = 1129.68, Z = 2, Dc = 1.528 g/cm3, μ = 0.692 mm^-1, F(000) = 1148, R = 0.064 and wR = 0.145 for 9571 observed reflections (I 〉 2σ(I)). In this polymer, the Mn(II) atoms adopt different coordination modes. The Mn(1) atom is five-coordinated, forming a distorted tetragonal pyramidal geometry. Mn(2) atom is six-coordinated to get a distorted octahedral geometry, which is different from the Mn(1) atom. Each Mn(II) atom is linked by aic ligands with neighboring Mn(II) atoms, forming an infinite one-dimensional (1D) double-chain structure. The existence of N–H…O hydrogen bonding interactions leads the 1D chains to generate a 2D structure. Luminescent properties for the ligand cipt and compound 1 have also been discussed in detail.
基金conducted in the framework of a project sponsored by the National Natural Science Foundation of China(No.21071100)Liaoning Baiqianwan Talents Program and the LNET(LJQ2011038)
文摘The coordination polymer, [Mn3(bpta)2(bip)2], (H3bpta = biphenyl-3,3',5-tricar- boxylic acid, bip = 2,6-bis(imidazole-1-yl)pyridine), has been synthesized under hydrothermal con- ditions and characterized by elemental analysis, FT-IR, XRD, TGA and single-crystal X-ray diffraction. It crystallizes in monoclinic, space group P21/c with a = 14.919(3), b = 9.780(2), c = 20.352(7) A, V = 2344.4(10) A3, Z= 2, C52H32Mn3N10012, Mr = 1153.70, Dc = 1.634 g/cm3, p(MoKa) = 0.876 mm-1, F(000) = 1170, the finalR = 0.0605 and wR = 0.1177. The complex forms a 2D layer with trinuclear Mn(II) units and further assembles into a 3D supramolecular network structure through C-H..'O hydrogen bonding and C-H...π interactions. Moreover, the negative J value indicates the presence of antiferromagnetic coupling between the Mn(II) ions within a trinuclear unit.
基金Supported by the Natural Science Foundation of Guangxi Province(No.2017GXNSFAA198268)the Foundation of Guangxi Key Laboratory of Electrochemical and Magneto-chemical Functional Materials(EMFM20161102)the National Natural Science Foundation of China(No.61765005)
文摘One new coordination polymer, [Mn(Hbtc)(bpy)(HO)]1, was synthesized by the reaction of manganese(Ⅱ) salt under pH-controlled hydrothermal conditions with unsymmetrical polycarboxylic acid of 1,2,4-benzenetricarboxylic acid(Hbtc) and 2,2?-bipyridine(bpy). The structure of complex 1 was characterized by single-crystal X-ray diffraction, IR spectra, powder X-ray analysis, thermal gravimetric analysis(TGA), UV-Vis spectrometry, photoluminescence and magnetic susceptibility. Complex 1 is a one-dimensional(1D) polymeric single-chain structure. Photoluminescence property is quite similar to the bpy ligand. Magnetic susceptibility measurement indicates that 1 shows a weak ferromagnetic coupling between the Mn~Ⅱ ions.
文摘The crystal structure and thermal stability of the martensite in Cu 24Al 3Mn (mole fraction, %) alloy were studied by X ray diffraction, electron diffraction, V - t curve measurement. The 18R martensite with fairly perfect long range order can be obtained by water quenching the alloy. The atoms distribution on the basal plane of the martensite is as follows: Ⅰ, 3/25 Mn+22/25 Cu; Ⅱ, 3/25 Al+22/25 Cu; Ⅲ, 18/25 Al+7/25 Cu, correspondingly, the parent phase may have Heusler structure. From the electron diffraction result, the crystal structure is determined to be of a modified 18R type but closely approaching orthorhombic 18R type, its lattice parameters are determined to be a = 0.447?4?nm, b = 0.522?9?nm, c = 3.815?nm and β =89.6° from the X ray diffraction results. The obtained alloy has a higher thermal stability than that of the conventional Cu Zn Al alloy.
基金Supported by the National Natural Science Foundation of China (No. 20271043)Natural Science Foundation of Shandong Province (Y2007B26)
文摘A three-dimensional coordination polymer [Mn2(μ1.3-N3)4(μ-PP)2]n (PP = 3-(pyrazin-2-yloxy)-pyridine) has been synthesized with 3-(pyrazin-2-yloxy)-pyridine and azide anion as mixed bridge ligand, and its crystal structure was determined by X-ray crystallography. The crystal data: triclinic system, space group P1, with a = 6.794(4), b = 9.885(6), c = 9.947(6) A, α = 64.170(6), β= 84.190(8), γ= 85.319(8)°, V = 597.7(6)A^3, Z = 1, C18H14Mn2N18O2, Mr = 624.35, Dc = 1.735 g/cm^3, F(000) = 314 and μ = 1.117 mm^-1. In the crystal, the azide anion acts as a bridge ligand and makes adjacent Mn(Ⅱ) ions connect into a two-dimensional sheet on the ab plane, then 3-(pyrazin-2-yloxy)-pyridine serves as a bidentate bridge ligand to connect neighboring sheets along
基金This work is financially supported by the National Natural Science Foundation of China ( No 50531020)
文摘NiMnGaferromagnetic shape memory thin film was deposited onto Al foil using r.f.magnetron sputtering technique.The crystallization behavior of the film was investigated by XRD and DSC.The activation energy of crystallization of the film was calculated by Kissinger’s method.The results show that the crystallization temperature of NiMnGafree-standing thin film in martensite state is 372 ℃,and the activation energy of crystallization is about 191.9 kJ·mol-1.
文摘The step pattern of single crystal growth and the morphology at equilibrium state of(Mn, Fe)S on the wall of micro-voids in ZG25 cast steel have been observed using scanning electron microscope.The face-centred cubic(Mn,Fe)S single crystal at equilibrium state is shown to be tetrakaidecahedron consisted of eight{111}planes and six{100}planes,and is a typical example of the O_h—m3m cubic crystal system.
基金This work was supported by the Natural Science Foundation of Jiangsu Province (No. BK200594) Science and Technology Development Foundation of Nanjing Agricultural University
文摘The title compound [Mn(DPMT)2Cl2(H2O)2] (DPMT = 1-[[2-(2,4-dichlorophenyl)- 1,3-dioxolan-2-yl]methyl]-1H-1,2,4-triazole) was synthesized by the reaction of MnCl2·4H2O and DPMT in ethanol solution and its structure was determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic, space group P21/c with a = 23.913(4), b = 7.8883(13), c = 8.6291(14)A, β = 95.816(3)°, V = 1619.4(5)A^3, Z = 2, C24H26Cl6MnN6O6, Mr = 762.15, Dc = 1.563 g/cm^3, μ = 0.950 mm^-1, S = 1.045, F(000) = 774, R = 0.0462 and wR = 0.0981. The molecular structure is a centrosymmetric conformation, and two ligands are symmetrically located on both sides of the Mn atom. The manganese atom is surrounded by two nitrogen atoms from ligands, two chlorine atoms and two oxygen atoms from water molecules to form a slightly distorted octahedral geometry.
文摘A novel coordination polymer [Mn(bcp)(bib)0.5]n(1, H2 bcp = 1,3-bis(4-carboxyphenoxy)propane and bib = 1,4-bis(imidazol-1-yl)benzene) was synthesized under hydrothermal conditions, and was characterized by single-crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectroscopy and powder X-ray diffraction(PXRD).Complex [Mn(bcp)(bib)0.5]n(1) is of triclinic system, space group P1 with a = 7.320(5), b =11.871(5), c = 13.932(5)?,α= 111.125(5)°,β= 99.658(5)°,γ= 101.104(5)°, Z = 2, V= 1070.3(9)?3 Mr = 474.34, Dc = 1.472 g/cm^3, F(000)= 488,μ= 0.660 mm^-1, the final R = 0.0353 and wR =0.0.984 for 4373 observed reflections with I > 2σ(I). Structure analysis reveals that complex 1 displays a rare 2 D + 2 D → 2 D polyrataxane topology. Moreover, the luminescent property for 1 was investigated at room temperature.
基金Supported by the Science and Technology Research Project of Hubei Provincial Department of Education(China,No.Q20174302)the Scientific Research Foundation of Jingchu University of Technology(No.QN201602)National college students innovation and entrepreneurship training program(No.201811336003,China)
文摘Tricyanide building block K[Ru(ttpy)(CN)3] and [MnⅢ(salen)](ClO4) have been used to design and synthesize a heterobimetallic one-dimensional(1D) zigzag chain complex 1,[RuⅡ(ttpy)(CN)3 MnⅢ(salen)](ttpy = 4′-(p-tolyl)-2,2′:6′,2″-terpyridine, salen = N,N?-ethylenebis-(salicylideneaminato)dianion). Single-crystal X-ray diffraction analysis shows complex 1 crystallizes in orthorhombic Pbca space group and the asymmetric unit of 1 contains one[-NC-RuⅡ(ttpy)(CN)(m-CN)-Mn Ⅲ-(salen)-] molecule. In the structure of 1, each [Ru Ⅱ(ttpy)(CN)3]-connects two [MnⅢ(salen)]+ with two cyanide groups in a cis-conformation, and in turn each[MnⅢ(salen)]+ unit links two [RuⅡ(ttpy)(CN)3]-building blocks in a trans-conformation, resulting in a 1D [-NC-RuⅡ-CN-MnⅢ-]n chain. Furthermore, the electronic absorption spectra and luminescence spectroscopy of complex 1 have also been studied.
基金Supported by the Construct Program of the Key Discipline in Hunan Province and Hengyang Bureau of Science & Technology (2005Cg10-23)
文摘A novel Mn(Ⅱ) complex Mn2(phen)2(p-MBA)4(H2O) has been hydrothermally synthesized by the reaction of p-methyl benzoic acid (p-MBA) with 1,10-phenanthroline (phen). Crystal data for this complex: monoclinic, space group C2/c, a= 2.3328(3), b =1.5549(2), c = 1.5557(2) nm, β = 121.726(2)°, V= 4.7997(11) nm^3, Mr = 1028.85, Dc = 1.424 g/cm^3, Z = 4, F(000) = 2128, μ(MoKa) = 0.590mm^-1, GOOF = 1.060, R = 0.0333 and wR = 0.0767. In the crystal, each Mn(Ⅱ) ion is coordinated by two nitrogen atoms from one o-phenanthroline molecule, three oxygen atoms from three p-methyl benzoic acids and one oxygen atom from one water molecule, giving a six-coordinate distorted octahedral coordination geometry. Two neighboring Mn(Ⅱ) ions are bridged by two p-methyl benzoic acid groups and one water molecule, and their end positions are respectively coordinated by one 1,10-phenanthroline and one p-methyl benzoic acid molecule, giving a binuclear cage structure, of which the Mn(Ⅱ)…Mn(Ⅱ) distance is 0.3502 nm.
基金Supported by the National Natural Science Foundation of China (No.20671064)Doctor Foundation of Liaoning Province (No.20071016)
文摘The 1-D chain coordination complex of {[Mn2(HCAM)3(H2bipy)]·5H2O}n (H3CAM = 4-hydroxypyridine-2,6-dicarboxylic acid, bipy = 4,4'-bipyridine) has been synthesized by the reaction of 4-hydroxypyridine-2,6-dicarboxylic acid, 4,4'-bipyridine and manganese carbonate under hydrothermal conditions, and its crystal structure was determined by X-ray diffraction method The crystal belongs to the monoclinic system, space group P21/n with a = 10.110(2), b = 20.159(4), c = 17.861(4)A,β = 99.67(3)°, V = 3.5884(12) nm3, Mr= 901.47, Z = 4, Dc= 1.669 g.cm^-3, μ= 0.798 mm^-1, F(000) = 1840, the final R = 0.0713 and ωR = 0.1853. The complex forms a 1-D chain bridged by HCAM, protonated 4,4-bipyridines link the 1-D chains to construct 2-D networks via N-H...O hydrogen bonds, and networks are further extended via π-π stacking and hydrogen bonds into 3-D supramolecular framework.
基金Supported by the National Natural Science Foundation of China(No.21461003)Natural Science Foundation of Guangxi Province(No.2016GXNSFFA380010,2016GXNSFAA380206,2014GXNSFBA118056)the Foundation of Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources,Ministry of Education of China(CMEMR2015-A11,CMEMR2016-A11)
文摘Based on a 3-(pyridine-2-yl)-4H-1,2,4-triazole ligand(Hpytr), one 2D Cd(Ⅱ) coordination polymer [Cd I(pytr)]n(1) and one 2D Mn(Ⅱ) coordination polymer [Mn(N3)(pytr)(H2O)]n(2) have been synthesized and characterized by X-ray crystallography, elemental analysis, and fluorescence spectroscopy. 1 shows a layer coordination architecture linked by pytr ligand, and the Cd(Ⅱ) centers display slightly distorted square pyramid coordination geometries. Complex 2 shows a 2D pillared-layer coordination architecture bridged by N3-and pytr, and the Mn(Ⅱ) centers display slightly distorted octahedral geometries. The luminescent properties of 1 and the PXRD and thermal stability of complexes 1 and 2 were measured briefly.
文摘Kinetics of oxygen adsorption on single crystal Mn<sub>5</sub>Si<sub>3</sub> (111) surface and initial surface oxidation were investigated. Oxygen chemisorbs dissociatively at room temperature on Mn and Si atoms. A fast oxidation of Si atoms occurs followed by oxidation of Mn atoms at RT. The MnO<sub>2</sub> was reduced by Si atoms and the SiO was oxidized further to SiO<sub>2</sub> during the sample heating.