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1.
Wang Qing-Lun Zhao Bin Liao Dai-Zheng Yan Shi-Ping Cheng Peng Jiang Zong-Hui 《Transition Metal Chemistry》2003,28(3):326-330
The copper(II) complex Na2[Cu(pba)] · 6H2O has been synthesized and its structure determined. It consists of a novel two-dimensional network of [Cu(pba)]2– anions connected to each other through the sodium ion as a bridge. Spectroscopic and magnetic properties have been measured and a spin distribution calculation has been carried out with the GAUSSIAN-94. Theoretical calculations indicate the rather larger spin density on nitrogen atoms should be responsible for the satellite lines appearing beside the main hyperfine coupling signs of copper(II). The antiferromagnetic interaction may be due to the intermolecular interaction and/or different copper(II) ions through the Na+ bridge in the same layer. 相似文献
2.
Shu-Lin Ma Zong-Hui Jiang Dai-Zheng Liao Shi-Ping Yan Geng-Lin Wang 《Transition Metal Chemistry》1994,19(5):531-533
Summary Two novel trinuclear complexes were prepared, namely [Cu2(oxae)2(H2O)2M] (ClO4)2, [oxae = N,N-bis(2-aminoethyl) oxamido dianion; M = Co and Ni]. Based on elemental analyses, conductivity measurements and i.r. spectra, the complexes are proposed to have extended oxamidobridged structures. The magnetic susceptibility of [Cu2-(oxae) 2(H2O)2Co](ClO4)2 were measured over the 4–300 K range and the observed data were successfully simulated by an equation based on the spin Hamiltonian, =–2J(1·2·2·3). The exchange integral, J, was found to be equal to –29.2 cm–1, indicating an antiferromagnetic spin-exchange interaction between the adjacent metal ions. 相似文献
3.
Chen-Xi Zhang Zhi-Liang Liu Dai-Zheng Liao Zong-Hui Jiang Shi-Ping Yan 《Journal of Molecular Structure》2003,650(1-3):21-26
A novel complex [Cu(NIT2Py)(PDA)(H2O)]·(CH3OH)(H2O) has been synthesized and structurally characterized by X-ray diffraction methods. It crystallizes in the monoclinic space group P2(1)/c. The structure consists of [Cu(NIT2Py)(PDA)(H2O)] moiety, one solvent methanol molecule and one water molecule. The copper(II) ion is in a distorted octahedral environment: one nitrogen atom and one oxygen atom from the NIT2Py, one nitrogen atom from the PDA (2,6-pyridine dicarboxylic acid) and one oxygen atom from the aqueous in the basal plane; two oxygen atoms from the PDA in the axial position. The units of [Cu(NIT2Py)(PDA)(H2O)] were connected as one dimension chain by the intermolecular hydrogen bonds. The complex exhibits intramolecular antiferromagnetic interactions between the Cu(II) ion and the NIT2Py. 相似文献
4.
LI Yan-Tuan LIAO Dai-Zheng JIANG Zong-Hui WANG Geng-LinDepartment of Chemistry Nankai University Tianjin China 《中国化学》1995,(3)
Six novel μ-oxamido heterobinuclear complexes, namely Cu(oxae)Ln(Me2bpy)2-(ClO4)3 (Ln=La, Nd, Gd, Tb, Ho, Er), where oxae denotes N, N'-bis(2-aminoethyl)oxamido dian-ion, Me2bpy is 4,4'-dimethyl-2,2'-bipyridyl, have been synthesized and characterized by elemental analyses, IR, conductivity measurements and electronic spectra. The temperature dependence of the magnetic susceptibility of Cu(oxae)Gd(Me2bpy)2(ClO4)3 has been meaured over the range 4-300 K. The least-squares fit of the experimental susceptibilities yielded J - 1.87 cm-1.The observed Gd(Ⅲ)-Cu(Ⅱ) coupling is ferromagnetic. One plausible mechanism that can cause a ferromagnetic coupling between Gd(Ⅲ) and Cu(Ⅱ) is discussed in terms of spin-polarization. 相似文献
5.
A series of novel two-dimensional (2D) and three-dimensional (3D) praseodymium coordination polymers, namely, {[Pr3(PDA)4(HPDA)(H2O)8] x 8H2O}n (2), {[Pr2(PDA)3(H2O)3] x H2O}n (3), {[Pr(PDA)(H2O)4] x ClO4}n (4), and { [Pr2(PDA)2(H2O)5SO4] x 2H2O}n (5) (PDA = pyridine-2,6-dicarboxylic anion), was designed and synthesized under hydrothermal conditions. Complexes 1-3 (chainlike polymer, {[Pr(PDA)(HPDA)(H2O)2] x 4H2O}n (1) was also obtained independently by us, although it has been reported recently by Ghosh et al.) were fabricated successfully by simply tuning the Pr/PDA ratio and exhibited various and intriguing topological structures from a 1D chain to a 3D network. While the synthetic strategy of 5 was triggered and further performed only after 1 was structurally characterized. The complexes were characterized by X-ray single-crystal determination, spectroscopic, and variable-temperature magnetic susceptibility analyses. In complex 2 an unusual nanosized square motif as a building block constructed by eight Pr ions was further assembled into a highly ordered 2D grid compound. In complex 3 the decanuclear Pr metal-based structure as a repeat unit interpenetrated to form a novel 3D polymer. Complex 4 was a 3D network polymer fabricated through a hexanuclear Pr ring as a building block, and ClO4- anions as guests were trapped in the cavity. In complex 5 six Pr atoms, two SO4(2-) anions, and carboxylic oxygen bridges constructed an intriguing rectangle structure as a repeat unit in the grid to form a 2D coordination polymer in which the unique bi-bidentate coordination mode of SO4(2-) anion was observed. 相似文献
6.
Summary Three novel heterotrinuclear complexes have been prepared, [Cu2(oxdn)2Zn](ClO4)2 (1) and [Cu2(oxdn)2-M(H2O)2](ClO4)2 with M=Mn (2) and Co (3) [oxdn-oxamidobis (propionato)], and characterized by spectral data. The temperature dependence of the magnetic susceptibilities of (2) and (3) has been studied in the 4–300K range, and the exchange integrals J=–20.90cm–1 for (2) and J=–62.36cm–1 for (3) calculated. These results are commensurate with antiferromagnetic interactions between the adjacent metal ions. 相似文献
7.
Yan Ouyang Wei Zhang Yue Ma Na Xu Dai-Zheng Liao Kazuyoshi Yoshimura Shi-Ping Yan 《Structural chemistry》2007,18(6):891-898
Two new tetranuclear complexes of macrocyclic oxamide [Cd(CuL)3](NO3)2·2.5H2O 1, [Mn(CuL)3(OH)2](ClO4)2·Mn(H2O)6·4.5H2O 2 (L = 1,4,8,11-tatraazacyclotradecanne-2,3-dione) have been synthesized, structurally characterized and preliminary investigated
by magnetic studies. The structures of the title complexes consist of a tetranuclear units MCu3 (M = Cd, Mn), the packing diagram shows two-dimensional and three-dimensional system through intermolecular weak interactions.
The temperature-dependent magnetic susceptibilities of complex 2 were analyzed by an approximate treatment leading to J = −33 cm−1, gCu = 2.10, gMn = 1.95 indicating antiferromagnetic exchange between Cu(II) and Mn(II) ions. 相似文献
8.
Bian HD Gu W Xu JY Bian F Yan SP Liao DZ Jiang ZH Cheng P 《Inorganic chemistry》2003,42(14):4265-4267
The first mu(3)-oxalato-bridged copper(II) complex, [[Cu(3)(L)(3)(mu(3)-C(2)O(4))][Cu(L)(H(2)O)](ClO(4))(2)] x 0.5(H(2)O) x 0.5(CH(3)OH), where HL = N-ethyl-N'-salicylidene-1,2-diaminoethane, has been synthesized and characterized by variable-temperature magnetic susceptibility measurement. The complex exhibits ferromagnetic coupling between the oxalato-bridged copper atoms and antiferromagnetic coupling between the oxygen-bridged copper atoms. 相似文献
9.
Si-Wei Zhang Dai-Zheng Liao Zong-Hui Jian Shi-Ping Yan Geng-Lin Wang 《Transition Metal Chemistry》1995,20(1):72-75
Summary New three CuII-CuII-CuII homotrinuclear complexes have been synthesized, namely [Cu(dmg)2{CuL}2](ClO4)2 [L = 5-nitro-1,10-phenanthroline (5-NO2-phen), 4,4-dimethyl-2,2-bipyridiine (DMbpy), tetramethylenediamine (TMDA) and dimethylglyoximate ion (dmg)2-]. The magnetic susceptibilities of complexes (1) (L = 5-NO2-phen) and (2) (L = DMbpy) were measured in the 4.2–300 K range, giving the parameters,J = -335cm-1 (1) andJ= -327.5cm-1 (2). The results demonstrate a very strong antiferromagnetic exchange interaction between the adjacent copper(II) ions. 相似文献
10.
Guang-Ming Yang Peng Cheng Dai-Zheng Liao Zong-Hui Jiang Shi-Ping Yan Geng-Lin Wang Xin-Kan Yao Hong-Gen Wang 《Journal of Cluster Science》1998,9(4):465-471
The preparation, magnetic properties, and crystal structure of [(salen)Cu]4[(salen)Fe(H2O)2]2(ClO4)2 via hydrogen bonding are described [salen=N,N-ethylenebis (salicylideneiminate)]. Crystals are triclinic, of space group
, with cell constants a=12.853(3), b=13.921(3), c=14.251(3) Å, =68.68(3)°, =87.86(3)°, =86.82(3)°, and Z=1. The structure was solved and refined to R=0.064 and R=0.068. The structure comprises the hexanuclear units which result from the linking of four mononuclear fragments [(salen)Cu] and two mononuclear fragment [(salen)Fe(H2O)]+, through Cu -O H -O -Fe -O -H O -Cu hydrogen bonds of coordinating H2O. In this complex, FeIII ions are in almost square-planar surroundings. The temperature dependences of the magnetic susceptibilities of the complex have been studied in the 4.2–300 K range, indicating the presence of an antiferromagnetic interactions between metal ions. 相似文献