Reaction of hydrated ytterbium nitrate and copper nitrate with diglycolic acid at pH= 7 produced a new Yb-Cu mixed metal complex, Yb2Cu3L6. 6H2O(L= O(CH2COO)2). Complex Yb2Cu3O36C2H36 (Mr= 1437. 23) crystallized in he...Reaction of hydrated ytterbium nitrate and copper nitrate with diglycolic acid at pH= 7 produced a new Yb-Cu mixed metal complex, Yb2Cu3L6. 6H2O(L= O(CH2COO)2). Complex Yb2Cu3O36C2H36 (Mr= 1437. 23) crystallized in hexagonalP6/mcc (No. 192) with cell parameters of a= 14. 344 (3), c= 15. 470(7) A,V= 2757(2) A 3; Z= 2; F(000) = 1390; Dcalc.= 1- 731 g/cm3 μ(MoKa) =45. 8 cm-1. The final agreernent factors are R= 0. 077 and Rw = 0.089 for 867 observed reflections with I>3δ(I). It has been characterized by elemental analysis, IR spectrum, magnetic measurement and X-ray crystallography. In the complex, the Yb3+ ion is 9-coordinated tothree ether oxygen and six carboxylate oxygen atoms from three ligands, the copper ionis coordinated to four oxygen atoms from four carboxylate groups of four ligands andtwo water molecules. The Yb3+ ions and the Cu2+ ions are connected by the carboxylate groups of the ligands, thus resulting in the formation of the complicated networkstructure.展开更多
The pentanuclear complex, [Cu5(SIP)2(HSIP)2(H2O)18](H2O)5 (H3SIP = 5-sulfoisophthalic acid), has been synthesized by the hydrothermal reaction of CuCI2 with NaH2SIP at 160 ℃, and characterized by single-cry...The pentanuclear complex, [Cu5(SIP)2(HSIP)2(H2O)18](H2O)5 (H3SIP = 5-sulfoisophthalic acid), has been synthesized by the hydrothermal reaction of CuCI2 with NaH2SIP at 160 ℃, and characterized by single-crystal X-ray diffraction and IR spectrum. The crystal of the complex crystallizes in a triclinic system, space group P^-1, with a = 7.0018(5), b = 11.9725(8), c = 19.0424(13)A^°, α = 78.8540(10), β = 85.1710(10), γ = 83.6080(10)°, V = 1553.24(19)A^°^3 Z = 1, C32H60O51S4Cu5, Mr= 1706.74, Dc= 1.825 g/cm^3,μ = 1.937 mm^-1, F(000) = 869, the final R = 0.0709 and wR = 0.1503 for 4235 observed reflections with I 〉 2σ(I). The five Cu^2+ ions are connected by two symmetry-related tddentate SIP^3- ligands and charge-balanced by two monodentate HSIP^2- ligands, giving a discrete pentanuclear structure. The pentanuclear copper molecules are linked by hydrogen bonds to form a three-dimensional supramolecular structure. The temperature-dependent magnetic susceptibility data revealed weak ferromagnetic magnetic interactions between the Cu^2+ ions.展开更多
Dibenzoyl peroxide undergoes oxidative addition on metallic copper powder with 2,2′-bipyridine(or imidazole)in a mixed solvent(methanol and tetrahydrofuran),and affords the Cu(Ⅱ)complexes-[Cu(Ce(C_6H_5COO)_2(2,2'...Dibenzoyl peroxide undergoes oxidative addition on metallic copper powder with 2,2′-bipyridine(or imidazole)in a mixed solvent(methanol and tetrahydrofuran),and affords the Cu(Ⅱ)complexes-[Cu(Ce(C_6H_5COO)_2(2,2'-bipy)]H_2O(1) and[Cu(C_6H_5COO)_2(C_3H_4N_2)_2](2).The structure was solved by direct methods and Fourier synthesis.C_(24)H_(20)N_2O_5Cu (1),Mr=479.78,space group P2(1)/c,a=6.986(7), b=18.833(I),c=17.021(3),α=γ=90°,Z=4,V=2218.1~3,Dc=1.443g/cm\+3,R=0.055 Rw=0.062.Complex(2),C_(20)H_(18)N_4O_4Cu(2),Mr=441.74,space group P2(1)/n,a=8.699(4), b=9.840(6),c=12.399(5),α=γ=90°,β=100.8°,Z=4,V=1010.9~3,Dc=1.654g/cm\+3,R=0.055, Rw=0.062.展开更多
A new copper(Ⅱ) complex [Cu2(MNA)2(2,2‘-bipy)2]·2.5H2 O with methy-5-norbornene-2,3-dicarboxylic acid(MNA) and 2,2’-bipyridine as ligands has been synthesized in the mixed solvents of DMF and water.It ...A new copper(Ⅱ) complex [Cu2(MNA)2(2,2‘-bipy)2]·2.5H2 O with methy-5-norbornene-2,3-dicarboxylic acid(MNA) and 2,2’-bipyridine as ligands has been synthesized in the mixed solvents of DMF and water.It crystallizes in monoclinic,space group P 1,with a = 10.4191(11),b = 12.8883(13),c = 16.1114(16) A,α = 70.8090(10),β = 80.568(2),γ = 77.440(2)o,V = 1984.3(4) A^3,Dc = 1.551 g/cm^3,Z = 2,F(000) = 962,the final GOOF = 1.051,R = 0.0431 and w R= 0.0980.The crystal structure shows that the whole molecule consists of two independent dinuclear units,in which two copper ions are bridged by two μ2-η^1:η^0 3-carboxylate groups of MNA^2-.The coordination environment of Cu(Ⅱ) ion is Cu O3N2,giving a distorted square pyramidal geometry.The spectroscopic characterization,thermal stability and magnetic properties of the complex were investigated.展开更多
A new copper(II) complex Cu2(L)a(2,2'-bipy)2(H2O)2 (1) has been synthesized with 2-benzoylbenzoic acid (HL) and 2,2'-bipyridin as ligands. The crystal belongs to a monoclinic system with space group Cc, ...A new copper(II) complex Cu2(L)a(2,2'-bipy)2(H2O)2 (1) has been synthesized with 2-benzoylbenzoic acid (HL) and 2,2'-bipyridin as ligands. The crystal belongs to a monoclinic system with space group Cc, a = 13.9979(II), b = 15.9888(13), c = 30.306(3) A, β = 100.8700(10)°, V= 6661.1(10) A3, Dc= 1.372 g/cm3, Z = 8, F(000) = 2840, the final GOOF = 1.018, R= 0.0685, and wR= 0.1731. There are two mononuclear Cu(L)2(2,2'-bipy)(H20) units in the crystal of 1. Each Cu(II) cation is coordinated by five atoms. The magnetic and fluorescent properties of 1 were studied. The results show that 1 exhibits weak paramagnetism, and when the excitation wavelength is at 616 nm, it has an intense fluorescent emission band around 482 nm.展开更多
A new dinuclear copper(Ⅱ) complex [Cu(CH3COO)(C7H5N4)(H2O)]2·3.5H2 O has been hydrothermally synthesized with copper acetate, o-acetamidobenzoic acid and 3-(pyridin-2-yl)-1,2,4-triazole. It crystallize...A new dinuclear copper(Ⅱ) complex [Cu(CH3COO)(C7H5N4)(H2O)]2·3.5H2 O has been hydrothermally synthesized with copper acetate, o-acetamidobenzoic acid and 3-(pyridin-2-yl)-1,2,4-triazole. It crystallizes in the monoclinic space group P21/c, with a = 12.0188(7), b = 13.7993(8), c = 8.7488(5) A, β = 101.7350(10)o, V = 1420.67(14) A3, D3 c = 1.568 g/cm, Z = 1, F(000) = 690, the final GOOF = 1.145, R = 0.0437, and w R = 0.1097. The crystal structure shows that the whole molecule consists of two copper ions bridged by two μ2-η1:η0 3-(pyridin-2-yl)-1,2,4-triazole anions. The coordination environment of Cu(Ⅱ) ion is Cu O2N3, giving a distorted square pyramidal geometry. The thermal stability and magnetic properties of the complex were investigated.展开更多
A series of copper (Ⅱ) complexes with pyridine N- oxide- 2- ylmethylidened-ithiocarbazates as ligands were synthesized and characterized by IR spectra, electronic spectra and magnetic moments measurement at room temp...A series of copper (Ⅱ) complexes with pyridine N- oxide- 2- ylmethylidened-ithiocarbazates as ligands were synthesized and characterized by IR spectra, electronic spectra and magnetic moments measurement at room temperature. Variable temperature magnetic susceptibilites (3-300K) of four complexs were measured and fitted with the Bleaney-Bowers dimer equation by considering the magnetic interaction between molecules. The fitting results show the existence of intramolecular ferromagnetic interactions and intermolecu-lar anti-ferromagnetic interactions in these copper( Ⅱ) complexes.展开更多
In the title coordination compound,[Cu(HDPPZC)(SO4)(H2O)]2 (1,HDPPZC=dipyrido[3,2-a:2,3-c]-phenazine-2-carboxylic acid),has been hydrothermally synthesized and characterized by single-crystal X-ray diffractio...In the title coordination compound,[Cu(HDPPZC)(SO4)(H2O)]2 (1,HDPPZC=dipyrido[3,2-a:2,3-c]-phenazine-2-carboxylic acid),has been hydrothermally synthesized and characterized by single-crystal X-ray diffraction,elemental analysis and magnetic susceptibility measurement.It crystallizes in triclinic,space group P1 with a=0.69485(6),b=0.76878(4),c=1.76638(13)nm,α=99.437(6),β=94.690(6),γ=95.735(6)o,V=0.92151(12) nm 3,Z=1,Cu2C38 H24 N 8S2O14,Mr=1007.85,Dc= 1.816 g·cm-3,F(000)=510,GOOF=0.988,the final R=0.0580 and wR=0.0689.The structural analyses reveal that complex 1 shows discrete dinuclear clusters,which are further linked by hydrogen bonding and π·π stacking interactions to form a three-dimensional supramolecular compound.Magnetic measurement shows ferromagnetic and antiferromagnetic exchange interactions in the sample.展开更多
A new binuclear copper(Ⅱ) complex [Cu2(Hpt)2(TNCA)2(H2O)2]·4 H2O(1) has been synthesized with copper acetate, 5-oxo-4-oxa-tricyclo[4.2.1.0]nonane-9-carboxylic acid(TNCA) and 3-(pyridin-2-yl)-1,2,4-...A new binuclear copper(Ⅱ) complex [Cu2(Hpt)2(TNCA)2(H2O)2]·4 H2O(1) has been synthesized with copper acetate, 5-oxo-4-oxa-tricyclo[4.2.1.0]nonane-9-carboxylic acid(TNCA) and 3-(pyridin-2-yl)-1,2,4-triazole(Hpt). It crystallizes in the triclinic space group P-1, with a = 8.8199(18), b = 14.278(3), c = 15.269(3) A, α = 76.21(3)o, β = 81.07(3)o, γ = 76.07(3)o, V = 1802.7(6) A3, Dc = 1.636 g/cm3, Z = 2, F(000) = 916, the final GOOF = 1.051, R = 0.0556 and wR = 0.1388. The whole molecule consists of two copper ions bridged by two μ2-η^1:η^0-3-(pyridin-2-yl)-1,2,4-triazole anions. The coordination environment of the Cu(1) ion is CuO2N3, giving a distorted square pyramidal geometry. 1 exhibits antiferromagnetic interaction between Cu(Ⅱ) ions, the electron transfer of 1 is irreversible in electrode reactions and the TG analysis shows that 1 is stable below 440 K.展开更多
A novel azide-bridged copper(Ⅱ) coordination polymer, [Cu3(NITpPy)4(N3)6]n (NITpPy = 4-pyridyl-4,4,5,5-tetramethylimidazline-3-oxide-1-oxyl), was structurally and magnetically characterized. It crystallizes i...A novel azide-bridged copper(Ⅱ) coordination polymer, [Cu3(NITpPy)4(N3)6]n (NITpPy = 4-pyridyl-4,4,5,5-tetramethylimidazline-3-oxide-1-oxyl), was structurally and magnetically characterized. It crystallizes in the triclinic space group P with a = 7.6932(10), b = 14.5556(19), c = 16.122(2) , α = 108.443(2), β = 95.251(2), γ = 104.236(2)°, V = 1631.7(4) 3, C48H64Cu3N30O8, Mr = 1379.87, Z = 1, Dc = 1.404 g/cm3, μ(MoKα) = 1.041 mm-1, F(000) = 713, the R = 0.0510 and wR = 0.1185 for 4285 observed reflections with I 2σ(I). X-ray analysis reveals that the Cu(Ⅱ) ions are linked by nitrogen atom of μ1,1 azido ligands to form a Cu-Cu-Cu unit. The units are linked by μ1,3 azido ligands through a bridging style to form a one-dimensional coordination polymer. The variable-temperature magnetic susceptibility data of the complex show ferromagnetic interactions in the complex.展开更多
At room temperature, the reaction of dibenzoyl peroxide with metallic copper powder in the presence of pyridine affords the copper(Ⅱ) complex [Cu(C 5H 5N) 2(H 2O)\|(C 6H 5COO) 2]. Crystal is monoclinic, M r =483.002,...At room temperature, the reaction of dibenzoyl peroxide with metallic copper powder in the presence of pyridine affords the copper(Ⅱ) complex [Cu(C 5H 5N) 2(H 2O)\|(C 6H 5COO) 2]. Crystal is monoclinic, M r =483.002, space group Cc with parameters: a=6\^078(4), b=15.879(4), c=23.091(3), β=97.61(2)°, V=2209.1(2) 3, Z=4, D c =1\^464g/cm 3, μ =10.279 cm -1 , F(000)=996, R=0\^031, R w =0.036, 1595 reflections with I≥3σ(I ) were considered to be observed. Each copper(Ⅱ) ion is coordinated by two monodentate benzoate ligands, two pyridines and one water molecule. The complex is also characterized by its IR, XPS and thermal properties.展开更多
At room temperature, dibenzoyl peroxide and pyridine N-oxide reacted with metallic copper powder in a mixed solvent(dichloromethane, trichloromethane and tetrahydrofuran), resulting in a binuclear copper(Ⅱ) complex. ...At room temperature, dibenzoyl peroxide and pyridine N-oxide reacted with metallic copper powder in a mixed solvent(dichloromethane, trichloromethane and tetrahydrofuran), resulting in a binuclear copper(Ⅱ) complex. [Cu (C_5H_5NO)-(C_6H_5COO)_2]_2. The structure of the complex was characterized by elemental analyses.IR spectra and X-ray single crystal analysis. The crystal is triclinic, space group P1,with cell parameters . a= 9. 262(4) ,b= 10. 697(2) , c=10. 881 (3 )A , a=59. 60( 2 ),β= 74. 83 ( 3 ) .Y = 72. 80 ( 2 )°. V= 880. 0 A ̄3 . D_c = 1 . 5 20 g/cm ̄3 . Z = 1 . μ= 1 2. 7 cm-1, R=0. 044 ,R_w=0. 048 for 3477 reflections with I>3σ(I), M_r=805. 78. Each copper(Ⅱ) atom is coordinated by four bridging bidentate benzoate ligands and one pyridine M-oxide.展开更多
MnZn ferrites with the chemical formula Mn0.68Zn0.25Fe2.07O4 have been prepared by a conventional ceramic technique. Then, the effects of CuO addition on the microstructure and temperature dependence of magnetic prope...MnZn ferrites with the chemical formula Mn0.68Zn0.25Fe2.07O4 have been prepared by a conventional ceramic technique. Then, the effects of CuO addition on the microstructure and temperature dependence of magnetic properties of MnZn ferrites were investigated by characterizing the fracture surface micrograph and measuring the magnetic properties over a temperature ranging from 25 to 120 C. The results show that the lattice constant and average grain size increase with the increase of CuO concentration. When the CuO concentration is below 0.07 wt.%, the initial permeability and saturation magnetic flux density increase monotonously, and the temperature of the secondary maximum peak in the curve of initial permeability versus temperature and the lowest power loss shift to a lower temperature with the increase of CuO concentra-tion. However, excessive CuO concentration (0.07 wt.%) results in abnormal grain growth and porosity increase, which causes the initial permeability and saturation magnetic flux density decrease and the power loss increase at room temperature. Furthermore, the temperature of the secondary maximum peak in the curve of initial permeability versus temperature and the lowest power loss shift to a higher temperature.展开更多
Two new copper complexes, [Cu(cbdc)(phen)(H2O)]·2H2O (1) and [Cu2(cbdc)(phen)2(H2O)2](ClO4)2·H2O (2) (cbdc= 1,1-cyclobutanedicarboxylate and phen= 1,10-phenanthroline), were synthesized b...Two new copper complexes, [Cu(cbdc)(phen)(H2O)]·2H2O (1) and [Cu2(cbdc)(phen)2(H2O)2](ClO4)2·H2O (2) (cbdc= 1,1-cyclobutanedicarboxylate and phen= 1,10-phenanthroline), were synthesized by reaction of cbdc with Cu(ClO4)2 and phen in ethanol aqueous solution. Complex 1 crystallizes in monoclinic system with space group P2(1)/c and a=0.9428(4) nm, b= 1.2183(5) nm, c= 1.6265(7) nm, β= 102.418(5)°, V= 1.8246(13) nm^3, Z=4, R=0.0445, wR2=0.0947. The structure of 1 is discretely mononuclear, which is packed by π…π interaction forming a 3D supramolecular structure where Cu(Ⅱ) ion is five-coordinated and has square-pyramidal coordination geometry. Its thermal decomposition procedure detail was studied by thermal analysis TG-DSC. Complex 2 belongs to monoclinic system with space group P2(1)/c and a=0.8897(3) nm, b= 1.9130(8) nm, c= 1.9936(8) nm,β=99.04(2)°, V=3.351(2) nm^3, Z=4, R=0.0540, wR2=0.1102. The structure of 2 is a discrete binucleus, where Cu(1) is four-coordinated by phen and cbdc in a square-planar geometry while Cu(2) is five-coordinated by phen, one O of cbdc and two H2O, which can be best described as distorted trigonal-bipyramidal geometry. Cu(1) and Cu(2) are linked by carboxylic group of cbdc in a bidentate bridging fashion. Variable-temperatttre magnetic susceptibilities of 2 in 2-300 K showed that its magnetic behavior obeyed Curie law.展开更多
Treatment of a heptadentate ligand 2,2'-(((pyridine-2,6-diyl-bis(methylene))- bis((pyridin-2-ylmethyl)azanediyl))bis(methylene))diphenol (H2L) possessing pyridinyl- and phenolate groups, with three eq...Treatment of a heptadentate ligand 2,2'-(((pyridine-2,6-diyl-bis(methylene))- bis((pyridin-2-ylmethyl)azanediyl))bis(methylene))diphenol (H2L) possessing pyridinyl- and phenolate groups, with three equivalents of Cu(C104)2·6H2O in methanol under base conditions, gave rise to a hexanuclear cluster complex [Cu6L2(OH)4](C104)4·4MeCN·0.5MeOH (1). Complex 1 crystallizes in triclinic, space group Pi with a = 12.068(12), b = 12.567(12), c = 16.279(16) A, α = 105.694(12), β = 93.631(13), γ = 112.017(11)°, V= 2166(4) A3, Z = 1,μ= 1.651 mm^-1, Dc = 1.599 Mg/m^3, T = 296(2) K, C74.5H795N14O24.5Cl4Cu6, Mr = 2086.12, F(000) = 1062.5, S = 1.061, R = 0.0521 and wR = 0.1270. In the cation of complex 1, the six copper cores are arranged into a two-parallel three-site strings configuration with each metal exhibits a slightly distorted square-pyramidal geometry, resulting from the connection of donor pyridinyi nitrogen and phenolate oxygen atoms in ligand H2L, and/or the oxygen donors in hydroxyl groups. In addition, magnetic susceptibility measurements revealed complex 1 displayed antiferromagnetic coupling.展开更多
Reaction of Cu with dibenzovi peroxide, 2-aminothiazol gave a binuclear complex [Cu_2 (C_6H_5COO)_4(C_3H_4N_2S)_2]. Crystal of the title compound is monoclinic system space group P2_1/n , M_r = 807. 84 with cell param...Reaction of Cu with dibenzovi peroxide, 2-aminothiazol gave a binuclear complex [Cu_2 (C_6H_5COO)_4(C_3H_4N_2S)_2]. Crystal of the title compound is monoclinic system space group P2_1/n , M_r = 807. 84 with cell parameters a= 10. 685 ( 1 ), b=19. 028(6), c=17. 046(9) , β=96. 49(33) ̄°, Z=4, V=3443. 4, D_c=1. 565 g/cm ̄-3, μ= 14. 078 cm ̄-1, F(000)= 824. The final refinement with 3429 observed reflections is converged with R= 0. 046 and R_w=0. 053. X-ray crystal structure analysis revealed that each copper ion is coordinated by four bridging birfentate benzoate ligandsand one Zaminothiazol to form a binuclear molecule. In the crvstal, there are intramolecular hydrogen bonds N (1)- H ( 1 )-O(4) and N (3)- H (3)-O(1) with NO distance of 3. 005, N-H-O angle of 131. 9°.展开更多
Dibenzoyl peroxide undergoes oxidative addition with metallic copper powder and 2, 2’-bipyridine in a mixed solvent (methanol and tetrahydrofuran ) to afford copper(Ⅱ) complex [Cu(2, 2’-bipy) (C<sub>6&...Dibenzoyl peroxide undergoes oxidative addition with metallic copper powder and 2, 2’-bipyridine in a mixed solvent (methanol and tetrahydrofuran ) to afford copper(Ⅱ) complex [Cu(2, 2’-bipy) (C<sub>6</sub>H<sub>5</sub>COO)<sub>2</sub>]· H<sub>2</sub>O. The structure of the cornplex was solved by direct methods and refined by block-diagonal and full-ma-trix least-squares method to a final R of 0. 055 for 2654 independent reflections of I 】3σ(I). Crystals are monoclinic,space group P2<sub>1</sub>/c , Mr= 479. 78 with cell parameters a= 6. 986(7) , b= 18. 833(1), c= 17. 021(3), β=97. 96(1)°, Z=4, Dc=1. 437g. cm ̄(-3), V= 2218. 1. Each copper ion is coordinated by the oxygen atoms of two benzoato groups and the nitrogen atoms of 2. 2’-bipyridine in a planar square geometry.展开更多
Two ternary complexes Cu2A4[OP(OCH3)3]2 (A represents CH2=CH-COO- and CH2=C(CH3)-COO-) have been synthesized, and elemental analyses, IR, ESR, electronic reflectance spectra and magnetic studies were carried out. The ...Two ternary complexes Cu2A4[OP(OCH3)3]2 (A represents CH2=CH-COO- and CH2=C(CH3)-COO-) have been synthesized, and elemental analyses, IR, ESR, electronic reflectance spectra and magnetic studies were carried out. The single crystal X-ray diffraction shows that Cu2[CH2=C(CH3)-COO]4[OP(OCH3)3]2 is triclinic, with space group P1, a = 1.05128(13), b = 1.7559(5), c = 1.94479(3) nm, α =91.263(14)°,(β = 102.559(6)°,γ= 106.339(13)°, Z = 4 and R = 0.0668. Two copper(Ⅱ) atoms are bridged by four (a-methacrylate groups, and each copper(Ⅱ) atom is coordinated with a trimethyl phosphate molecule in the axial position, forming a distorted square pyramidal configuration. The symmetric center is between the two copper(Ⅱ) atoms, and the Cu-Cu bond distance is 0.26098(6) nm. The Cu-Cu distance and magnetic studies suggest that there exist anti-ferromagnetic interactions between the two copper(Ⅱ) atoms.展开更多
文摘Reaction of hydrated ytterbium nitrate and copper nitrate with diglycolic acid at pH= 7 produced a new Yb-Cu mixed metal complex, Yb2Cu3L6. 6H2O(L= O(CH2COO)2). Complex Yb2Cu3O36C2H36 (Mr= 1437. 23) crystallized in hexagonalP6/mcc (No. 192) with cell parameters of a= 14. 344 (3), c= 15. 470(7) A,V= 2757(2) A 3; Z= 2; F(000) = 1390; Dcalc.= 1- 731 g/cm3 μ(MoKa) =45. 8 cm-1. The final agreernent factors are R= 0. 077 and Rw = 0.089 for 867 observed reflections with I>3δ(I). It has been characterized by elemental analysis, IR spectrum, magnetic measurement and X-ray crystallography. In the complex, the Yb3+ ion is 9-coordinated tothree ether oxygen and six carboxylate oxygen atoms from three ligands, the copper ionis coordinated to four oxygen atoms from four carboxylate groups of four ligands andtwo water molecules. The Yb3+ ions and the Cu2+ ions are connected by the carboxylate groups of the ligands, thus resulting in the formation of the complicated networkstructure.
基金Supported by the Education Department of Jiangxi Province (No. 2007-125)Jiangxi Normal University
文摘The pentanuclear complex, [Cu5(SIP)2(HSIP)2(H2O)18](H2O)5 (H3SIP = 5-sulfoisophthalic acid), has been synthesized by the hydrothermal reaction of CuCI2 with NaH2SIP at 160 ℃, and characterized by single-crystal X-ray diffraction and IR spectrum. The crystal of the complex crystallizes in a triclinic system, space group P^-1, with a = 7.0018(5), b = 11.9725(8), c = 19.0424(13)A^°, α = 78.8540(10), β = 85.1710(10), γ = 83.6080(10)°, V = 1553.24(19)A^°^3 Z = 1, C32H60O51S4Cu5, Mr= 1706.74, Dc= 1.825 g/cm^3,μ = 1.937 mm^-1, F(000) = 869, the final R = 0.0709 and wR = 0.1503 for 4235 observed reflections with I 〉 2σ(I). The five Cu^2+ ions are connected by two symmetry-related tddentate SIP^3- ligands and charge-balanced by two monodentate HSIP^2- ligands, giving a discrete pentanuclear structure. The pentanuclear copper molecules are linked by hydrogen bonds to form a three-dimensional supramolecular structure. The temperature-dependent magnetic susceptibility data revealed weak ferromagnetic magnetic interactions between the Cu^2+ ions.
文摘Dibenzoyl peroxide undergoes oxidative addition on metallic copper powder with 2,2′-bipyridine(or imidazole)in a mixed solvent(methanol and tetrahydrofuran),and affords the Cu(Ⅱ)complexes-[Cu(Ce(C_6H_5COO)_2(2,2'-bipy)]H_2O(1) and[Cu(C_6H_5COO)_2(C_3H_4N_2)_2](2).The structure was solved by direct methods and Fourier synthesis.C_(24)H_(20)N_2O_5Cu (1),Mr=479.78,space group P2(1)/c,a=6.986(7), b=18.833(I),c=17.021(3),α=γ=90°,Z=4,V=2218.1~3,Dc=1.443g/cm\+3,R=0.055 Rw=0.062.Complex(2),C_(20)H_(18)N_4O_4Cu(2),Mr=441.74,space group P2(1)/n,a=8.699(4), b=9.840(6),c=12.399(5),α=γ=90°,β=100.8°,Z=4,V=1010.9~3,Dc=1.654g/cm\+3,R=0.055, Rw=0.062.
基金Supported by the Natural Science Foundation of Hunan Province(No.11JJ9006)Key Project of Science and Technology Plan of Hunan Province(2012FJ2002)the Construct Program of the Key Discipline in Hunan Province
文摘A new copper(Ⅱ) complex [Cu2(MNA)2(2,2‘-bipy)2]·2.5H2 O with methy-5-norbornene-2,3-dicarboxylic acid(MNA) and 2,2’-bipyridine as ligands has been synthesized in the mixed solvents of DMF and water.It crystallizes in monoclinic,space group P 1,with a = 10.4191(11),b = 12.8883(13),c = 16.1114(16) A,α = 70.8090(10),β = 80.568(2),γ = 77.440(2)o,V = 1984.3(4) A^3,Dc = 1.551 g/cm^3,Z = 2,F(000) = 962,the final GOOF = 1.051,R = 0.0431 and w R= 0.0980.The crystal structure shows that the whole molecule consists of two independent dinuclear units,in which two copper ions are bridged by two μ2-η^1:η^0 3-carboxylate groups of MNA^2-.The coordination environment of Cu(Ⅱ) ion is Cu O3N2,giving a distorted square pyramidal geometry.The spectroscopic characterization,thermal stability and magnetic properties of the complex were investigated.
基金Supported by the Fund of Science and Technology Committee of Hunan Province(No.2012GK3030)Scientific Research Fund of Hunan Provincial Education Department(No.11C0186)Key Project of Science and Technology Plan of Hunan Province(2012FJ2002)
文摘A new copper(II) complex Cu2(L)a(2,2'-bipy)2(H2O)2 (1) has been synthesized with 2-benzoylbenzoic acid (HL) and 2,2'-bipyridin as ligands. The crystal belongs to a monoclinic system with space group Cc, a = 13.9979(II), b = 15.9888(13), c = 30.306(3) A, β = 100.8700(10)°, V= 6661.1(10) A3, Dc= 1.372 g/cm3, Z = 8, F(000) = 2840, the final GOOF = 1.018, R= 0.0685, and wR= 0.1731. There are two mononuclear Cu(L)2(2,2'-bipy)(H20) units in the crystal of 1. Each Cu(II) cation is coordinated by five atoms. The magnetic and fluorescent properties of 1 were studied. The results show that 1 exhibits weak paramagnetism, and when the excitation wavelength is at 616 nm, it has an intense fluorescent emission band around 482 nm.
基金Supported by the Construct Program of the Key Discipline in Hunan Province and Key Project of Production Plan of Hengyang City(2013)
文摘A new dinuclear copper(Ⅱ) complex [Cu(CH3COO)(C7H5N4)(H2O)]2·3.5H2 O has been hydrothermally synthesized with copper acetate, o-acetamidobenzoic acid and 3-(pyridin-2-yl)-1,2,4-triazole. It crystallizes in the monoclinic space group P21/c, with a = 12.0188(7), b = 13.7993(8), c = 8.7488(5) A, β = 101.7350(10)o, V = 1420.67(14) A3, D3 c = 1.568 g/cm, Z = 1, F(000) = 690, the final GOOF = 1.145, R = 0.0437, and w R = 0.1097. The crystal structure shows that the whole molecule consists of two copper ions bridged by two μ2-η1:η0 3-(pyridin-2-yl)-1,2,4-triazole anions. The coordination environment of Cu(Ⅱ) ion is Cu O2N3, giving a distorted square pyramidal geometry. The thermal stability and magnetic properties of the complex were investigated.
文摘A series of copper (Ⅱ) complexes with pyridine N- oxide- 2- ylmethylidened-ithiocarbazates as ligands were synthesized and characterized by IR spectra, electronic spectra and magnetic moments measurement at room temperature. Variable temperature magnetic susceptibilites (3-300K) of four complexs were measured and fitted with the Bleaney-Bowers dimer equation by considering the magnetic interaction between molecules. The fitting results show the existence of intramolecular ferromagnetic interactions and intermolecu-lar anti-ferromagnetic interactions in these copper( Ⅱ) complexes.
基金Key Project of Chinese Ministry of Education (No. 210053)Jiangsu University (Nos. 09JDG001,1281310029)
文摘In the title coordination compound,[Cu(HDPPZC)(SO4)(H2O)]2 (1,HDPPZC=dipyrido[3,2-a:2,3-c]-phenazine-2-carboxylic acid),has been hydrothermally synthesized and characterized by single-crystal X-ray diffraction,elemental analysis and magnetic susceptibility measurement.It crystallizes in triclinic,space group P1 with a=0.69485(6),b=0.76878(4),c=1.76638(13)nm,α=99.437(6),β=94.690(6),γ=95.735(6)o,V=0.92151(12) nm 3,Z=1,Cu2C38 H24 N 8S2O14,Mr=1007.85,Dc= 1.816 g·cm-3,F(000)=510,GOOF=0.988,the final R=0.0580 and wR=0.0689.The structural analyses reveal that complex 1 shows discrete dinuclear clusters,which are further linked by hydrogen bonding and π·π stacking interactions to form a three-dimensional supramolecular compound.Magnetic measurement shows ferromagnetic and antiferromagnetic exchange interactions in the sample.
基金Supported by the Scientific Research Found of Hunan Provincial Education Department of China(17A049,17C0226)Industry and Research Key Project of Hengyang City(2017KJ155,2017KJ193)Doctoral Scientific Research Foundation of Hengyang Normal University(17D01)
文摘A new binuclear copper(Ⅱ) complex [Cu2(Hpt)2(TNCA)2(H2O)2]·4 H2O(1) has been synthesized with copper acetate, 5-oxo-4-oxa-tricyclo[4.2.1.0]nonane-9-carboxylic acid(TNCA) and 3-(pyridin-2-yl)-1,2,4-triazole(Hpt). It crystallizes in the triclinic space group P-1, with a = 8.8199(18), b = 14.278(3), c = 15.269(3) A, α = 76.21(3)o, β = 81.07(3)o, γ = 76.07(3)o, V = 1802.7(6) A3, Dc = 1.636 g/cm3, Z = 2, F(000) = 916, the final GOOF = 1.051, R = 0.0556 and wR = 0.1388. The whole molecule consists of two copper ions bridged by two μ2-η^1:η^0-3-(pyridin-2-yl)-1,2,4-triazole anions. The coordination environment of the Cu(1) ion is CuO2N3, giving a distorted square pyramidal geometry. 1 exhibits antiferromagnetic interaction between Cu(Ⅱ) ions, the electron transfer of 1 is irreversible in electrode reactions and the TG analysis shows that 1 is stable below 440 K.
基金supported by the National Natural Science Foundations of China (Nos. 20771054 and 21071074)
文摘A novel azide-bridged copper(Ⅱ) coordination polymer, [Cu3(NITpPy)4(N3)6]n (NITpPy = 4-pyridyl-4,4,5,5-tetramethylimidazline-3-oxide-1-oxyl), was structurally and magnetically characterized. It crystallizes in the triclinic space group P with a = 7.6932(10), b = 14.5556(19), c = 16.122(2) , α = 108.443(2), β = 95.251(2), γ = 104.236(2)°, V = 1631.7(4) 3, C48H64Cu3N30O8, Mr = 1379.87, Z = 1, Dc = 1.404 g/cm3, μ(MoKα) = 1.041 mm-1, F(000) = 713, the R = 0.0510 and wR = 0.1185 for 4285 observed reflections with I 2σ(I). X-ray analysis reveals that the Cu(Ⅱ) ions are linked by nitrogen atom of μ1,1 azido ligands to form a Cu-Cu-Cu unit. The units are linked by μ1,3 azido ligands through a bridging style to form a one-dimensional coordination polymer. The variable-temperature magnetic susceptibility data of the complex show ferromagnetic interactions in the complex.
文摘At room temperature, the reaction of dibenzoyl peroxide with metallic copper powder in the presence of pyridine affords the copper(Ⅱ) complex [Cu(C 5H 5N) 2(H 2O)\|(C 6H 5COO) 2]. Crystal is monoclinic, M r =483.002, space group Cc with parameters: a=6\^078(4), b=15.879(4), c=23.091(3), β=97.61(2)°, V=2209.1(2) 3, Z=4, D c =1\^464g/cm 3, μ =10.279 cm -1 , F(000)=996, R=0\^031, R w =0.036, 1595 reflections with I≥3σ(I ) were considered to be observed. Each copper(Ⅱ) ion is coordinated by two monodentate benzoate ligands, two pyridines and one water molecule. The complex is also characterized by its IR, XPS and thermal properties.
文摘At room temperature, dibenzoyl peroxide and pyridine N-oxide reacted with metallic copper powder in a mixed solvent(dichloromethane, trichloromethane and tetrahydrofuran), resulting in a binuclear copper(Ⅱ) complex. [Cu (C_5H_5NO)-(C_6H_5COO)_2]_2. The structure of the complex was characterized by elemental analyses.IR spectra and X-ray single crystal analysis. The crystal is triclinic, space group P1,with cell parameters . a= 9. 262(4) ,b= 10. 697(2) , c=10. 881 (3 )A , a=59. 60( 2 ),β= 74. 83 ( 3 ) .Y = 72. 80 ( 2 )°. V= 880. 0 A ̄3 . D_c = 1 . 5 20 g/cm ̄3 . Z = 1 . μ= 1 2. 7 cm-1, R=0. 044 ,R_w=0. 048 for 3477 reflections with I>3σ(I), M_r=805. 78. Each copper(Ⅱ) atom is coordinated by four bridging bidentate benzoate ligands and one pyridine M-oxide.
文摘MnZn ferrites with the chemical formula Mn0.68Zn0.25Fe2.07O4 have been prepared by a conventional ceramic technique. Then, the effects of CuO addition on the microstructure and temperature dependence of magnetic properties of MnZn ferrites were investigated by characterizing the fracture surface micrograph and measuring the magnetic properties over a temperature ranging from 25 to 120 C. The results show that the lattice constant and average grain size increase with the increase of CuO concentration. When the CuO concentration is below 0.07 wt.%, the initial permeability and saturation magnetic flux density increase monotonously, and the temperature of the secondary maximum peak in the curve of initial permeability versus temperature and the lowest power loss shift to a lower temperature with the increase of CuO concentra-tion. However, excessive CuO concentration (0.07 wt.%) results in abnormal grain growth and porosity increase, which causes the initial permeability and saturation magnetic flux density decrease and the power loss increase at room temperature. Furthermore, the temperature of the secondary maximum peak in the curve of initial permeability versus temperature and the lowest power loss shift to a higher temperature.
文摘Two new copper complexes, [Cu(cbdc)(phen)(H2O)]·2H2O (1) and [Cu2(cbdc)(phen)2(H2O)2](ClO4)2·H2O (2) (cbdc= 1,1-cyclobutanedicarboxylate and phen= 1,10-phenanthroline), were synthesized by reaction of cbdc with Cu(ClO4)2 and phen in ethanol aqueous solution. Complex 1 crystallizes in monoclinic system with space group P2(1)/c and a=0.9428(4) nm, b= 1.2183(5) nm, c= 1.6265(7) nm, β= 102.418(5)°, V= 1.8246(13) nm^3, Z=4, R=0.0445, wR2=0.0947. The structure of 1 is discretely mononuclear, which is packed by π…π interaction forming a 3D supramolecular structure where Cu(Ⅱ) ion is five-coordinated and has square-pyramidal coordination geometry. Its thermal decomposition procedure detail was studied by thermal analysis TG-DSC. Complex 2 belongs to monoclinic system with space group P2(1)/c and a=0.8897(3) nm, b= 1.9130(8) nm, c= 1.9936(8) nm,β=99.04(2)°, V=3.351(2) nm^3, Z=4, R=0.0540, wR2=0.1102. The structure of 2 is a discrete binucleus, where Cu(1) is four-coordinated by phen and cbdc in a square-planar geometry while Cu(2) is five-coordinated by phen, one O of cbdc and two H2O, which can be best described as distorted trigonal-bipyramidal geometry. Cu(1) and Cu(2) are linked by carboxylic group of cbdc in a bidentate bridging fashion. Variable-temperatttre magnetic susceptibilities of 2 in 2-300 K showed that its magnetic behavior obeyed Curie law.
基金Financially supported by the Education Department of Jiangxi Province(No.JXJG-14-10-6)Jiangxi Science and Technology Normal University
文摘Treatment of a heptadentate ligand 2,2'-(((pyridine-2,6-diyl-bis(methylene))- bis((pyridin-2-ylmethyl)azanediyl))bis(methylene))diphenol (H2L) possessing pyridinyl- and phenolate groups, with three equivalents of Cu(C104)2·6H2O in methanol under base conditions, gave rise to a hexanuclear cluster complex [Cu6L2(OH)4](C104)4·4MeCN·0.5MeOH (1). Complex 1 crystallizes in triclinic, space group Pi with a = 12.068(12), b = 12.567(12), c = 16.279(16) A, α = 105.694(12), β = 93.631(13), γ = 112.017(11)°, V= 2166(4) A3, Z = 1,μ= 1.651 mm^-1, Dc = 1.599 Mg/m^3, T = 296(2) K, C74.5H795N14O24.5Cl4Cu6, Mr = 2086.12, F(000) = 1062.5, S = 1.061, R = 0.0521 and wR = 0.1270. In the cation of complex 1, the six copper cores are arranged into a two-parallel three-site strings configuration with each metal exhibits a slightly distorted square-pyramidal geometry, resulting from the connection of donor pyridinyi nitrogen and phenolate oxygen atoms in ligand H2L, and/or the oxygen donors in hydroxyl groups. In addition, magnetic susceptibility measurements revealed complex 1 displayed antiferromagnetic coupling.
文摘Reaction of Cu with dibenzovi peroxide, 2-aminothiazol gave a binuclear complex [Cu_2 (C_6H_5COO)_4(C_3H_4N_2S)_2]. Crystal of the title compound is monoclinic system space group P2_1/n , M_r = 807. 84 with cell parameters a= 10. 685 ( 1 ), b=19. 028(6), c=17. 046(9) , β=96. 49(33) ̄°, Z=4, V=3443. 4, D_c=1. 565 g/cm ̄-3, μ= 14. 078 cm ̄-1, F(000)= 824. The final refinement with 3429 observed reflections is converged with R= 0. 046 and R_w=0. 053. X-ray crystal structure analysis revealed that each copper ion is coordinated by four bridging birfentate benzoate ligandsand one Zaminothiazol to form a binuclear molecule. In the crvstal, there are intramolecular hydrogen bonds N (1)- H ( 1 )-O(4) and N (3)- H (3)-O(1) with NO distance of 3. 005, N-H-O angle of 131. 9°.
文摘Dibenzoyl peroxide undergoes oxidative addition with metallic copper powder and 2, 2’-bipyridine in a mixed solvent (methanol and tetrahydrofuran ) to afford copper(Ⅱ) complex [Cu(2, 2’-bipy) (C<sub>6</sub>H<sub>5</sub>COO)<sub>2</sub>]· H<sub>2</sub>O. The structure of the cornplex was solved by direct methods and refined by block-diagonal and full-ma-trix least-squares method to a final R of 0. 055 for 2654 independent reflections of I 】3σ(I). Crystals are monoclinic,space group P2<sub>1</sub>/c , Mr= 479. 78 with cell parameters a= 6. 986(7) , b= 18. 833(1), c= 17. 021(3), β=97. 96(1)°, Z=4, Dc=1. 437g. cm ̄(-3), V= 2218. 1. Each copper ion is coordinated by the oxygen atoms of two benzoato groups and the nitrogen atoms of 2. 2’-bipyridine in a planar square geometry.
基金This work was supported by the National Natural Science Foundation of China (Grant No. 29831010) and the Foundation of the State Key Laboratory of Coordination Chemistry of Nanjing University.
文摘Two ternary complexes Cu2A4[OP(OCH3)3]2 (A represents CH2=CH-COO- and CH2=C(CH3)-COO-) have been synthesized, and elemental analyses, IR, ESR, electronic reflectance spectra and magnetic studies were carried out. The single crystal X-ray diffraction shows that Cu2[CH2=C(CH3)-COO]4[OP(OCH3)3]2 is triclinic, with space group P1, a = 1.05128(13), b = 1.7559(5), c = 1.94479(3) nm, α =91.263(14)°,(β = 102.559(6)°,γ= 106.339(13)°, Z = 4 and R = 0.0668. Two copper(Ⅱ) atoms are bridged by four (a-methacrylate groups, and each copper(Ⅱ) atom is coordinated with a trimethyl phosphate molecule in the axial position, forming a distorted square pyramidal configuration. The symmetric center is between the two copper(Ⅱ) atoms, and the Cu-Cu bond distance is 0.26098(6) nm. The Cu-Cu distance and magnetic studies suggest that there exist anti-ferromagnetic interactions between the two copper(Ⅱ) atoms.