The reaction behavior of forming the hetero-nuclear β-type chelates of rare earth ions (RE 3+) with p-sulphoaminobromophosphonazo(BPA-pSN) in ClCH_2COOH-CH_3COONa buffer solutions were studied by a spectrophotometri...The reaction behavior of forming the hetero-nuclear β-type chelates of rare earth ions (RE 3+) with p-sulphoaminobromophosphonazo(BPA-pSN) in ClCH_2COOH-CH_3COONa buffer solutions were studied by a spectrophotometric method. The interaction of RE 3+ with BPA-pSN, which can forms hetero-nuclear β-type chelates having composition ratio of RE_1 (light rare earth):BPA-pSN:RE_2(heavy rare earth ion)=1∶3∶1, is a first-order reaction. Meanwhile, BPA-pSN can only forms homo-nuclear β-type chelates with heavy rare earth ions, having a composition ratio of RE∶BPA-pSN=1∶2 and being a second-order reaction. The rate constants of forming homo-and hetero-nuclear β-type chelates were obtained and the mechanism of forming hetero-nuclear β-type chelates was proposed.展开更多
A novel 3D hetero-nuclear framework,namely [K_2Cd_5（Hbptc）_4（H_2O）_（12）·12H_2O]_n（1,H4 bptc = biphenyl-2,3,3？,5？-tetracarboxylic acid）,was obtained by hydrothermal reaction. X-ray singlecrystal structur...A novel 3D hetero-nuclear framework,namely [K_2Cd_5（Hbptc）_4（H_2O）_（12）·12H_2O]_n（1,H4 bptc = biphenyl-2,3,3？,5？-tetracarboxylic acid）,was obtained by hydrothermal reaction. X-ray singlecrystal structure analysis reveals that polymer 1 crystallizes in orthorhombic,space group Pbcn with a = 26.6152（13）,b = 11.7449（5）,c = 29.5923（14） ？,V = 9250.3（7） ？~3,C_（64）H_（76）Cd_5K_2O_（56）,Mr = 2381.44,Dc = 1.710 g/cm^3,μ（MoK α） = 1.323 mm^（-1）,F（000） = 4744,Z = 4,the final R = 0.0668 and wR = 0.1135 for 10613 observed reflections（I 〉 2σ（I））. Polymer 1 displays a 3D network that is built on the unprecedented heterobimetallic [Cd_3Cd_2K] molecular building block with a（3,4）-connected（6·8·8）2（6·6·82·82·126·126） topology which represents a rare 2-fold interpenetrating 3D framework topology network. The luminescence analyses reveal that polymer 1 shows obvious emission at room temperature in the solid state. In addition,it was also characterized by elemental,IR spectra and TG analyses.展开更多
A novel heteronuclear metal organic framework(MOF) incorporating both transition and alkali metal ions, namely, {(Ni_2K_2L_2·bipy]×6 H_2O]×2 H_2O}n(1, L = N-phosphonomethyl amino diacetic acid, bipy = 4...A novel heteronuclear metal organic framework(MOF) incorporating both transition and alkali metal ions, namely, {(Ni_2K_2L_2·bipy]×6 H_2O]×2 H_2O}n(1, L = N-phosphonomethyl amino diacetic acid, bipy = 4,4?-dipyridine) has been obtained. Its structure was established by single-crystal X-ray diffraction analysis and further characterized by elemental analysis and IR spectroscopy. The complex crystallizes in orthorhombic system, space group Pccn with a = 14.650(11), b = 36.56(3), c = 7.112(5) ? and V = 3809.3(8) ?~3. In this framework, bipy connects adjacent Ni–K heteronuclear coordination units into 1 D railway type chains, which are further propagated into 2 D deck-like array bearing large tunnels through the carboxylic oxygen from N-phosphonomethyl amino diacetic acid. The molar electrical conductivity of heteronuclear complex increases gradually with increasing the temperature. Complex 1 also exhibits strong photoluminescent emission in the visible region.展开更多
The photodetachment of a hetero-nuclear diatomic molecular negative ion is studied by using a two-centre model. An analytic formula is presented for the electron flux distribution of a heteronuclear diatomic molecular...The photodetachment of a hetero-nuclear diatomic molecular negative ion is studied by using a two-centre model. An analytic formula is presented for the electron flux distribution of a heteronuclear diatomic molecular negative ion. Taking HF- as an example, we calculated the electron flux distributions of this ion for various detached electron energies. The results show that the electron flux distributions exhibit oscillatory structures, which are caused by the interference effect between the two nuclei. Besides, the laser light polarization also has a great influence on the electron flux distribution. The oscillation amplitude is the largest when the laser polarization is parallel to the z-axis; when the laser polarization is perpendicular to the z-axis, the oscillation almost vanishes. This study provides a new understanding of the photodetachment of a heteronuclear diatomic molecular negative ion.展开更多
A new hetero-six-nuclear cluster was synthesized and determined by X-ray diffraction technique. The four-carboxylate groups are bound to the Cu(II) atoms to form Cu(OR)4Cu paddle-wheel-type cage between two DMF as the...A new hetero-six-nuclear cluster was synthesized and determined by X-ray diffraction technique. The four-carboxylate groups are bound to the Cu(II) atoms to form Cu(OR)4Cu paddle-wheel-type cage between two DMF as the basis for the cluster. The distance of two copper(II) atoms is 2.642 ?, and they are bridged by the carboxylate groups. A huge system plane was auto-assembled by four host molecules and two Cu (II) ions, which was observed in the crystal structure.展开更多
文摘The reaction behavior of forming the hetero-nuclear β-type chelates of rare earth ions (RE 3+) with p-sulphoaminobromophosphonazo(BPA-pSN) in ClCH_2COOH-CH_3COONa buffer solutions were studied by a spectrophotometric method. The interaction of RE 3+ with BPA-pSN, which can forms hetero-nuclear β-type chelates having composition ratio of RE_1 (light rare earth):BPA-pSN:RE_2(heavy rare earth ion)=1∶3∶1, is a first-order reaction. Meanwhile, BPA-pSN can only forms homo-nuclear β-type chelates with heavy rare earth ions, having a composition ratio of RE∶BPA-pSN=1∶2 and being a second-order reaction. The rate constants of forming homo-and hetero-nuclear β-type chelates were obtained and the mechanism of forming hetero-nuclear β-type chelates was proposed.
基金supported by the National Natural Science Foundation of China(No.21273101 and 21302082)the Program for Science&Technology Innovation Talents in Universities of Henan Province(2014HASTIT014,14IRTSTHN008 and 164100510012)the Tackle Key Problem of Science and Technology Project of Henan Province(No.142102310483)
文摘A novel 3D hetero-nuclear framework,namely [K_2Cd_5（Hbptc）_4（H_2O）_（12）·12H_2O]_n（1,H4 bptc = biphenyl-2,3,3？,5？-tetracarboxylic acid）,was obtained by hydrothermal reaction. X-ray singlecrystal structure analysis reveals that polymer 1 crystallizes in orthorhombic,space group Pbcn with a = 26.6152（13）,b = 11.7449（5）,c = 29.5923（14） ？,V = 9250.3（7） ？~3,C_（64）H_（76）Cd_5K_2O_（56）,Mr = 2381.44,Dc = 1.710 g/cm^3,μ（MoK α） = 1.323 mm^（-1）,F（000） = 4744,Z = 4,the final R = 0.0668 and wR = 0.1135 for 10613 observed reflections（I 〉 2σ（I））. Polymer 1 displays a 3D network that is built on the unprecedented heterobimetallic [Cd_3Cd_2K] molecular building block with a（3,4）-connected（6·8·8）2（6·6·82·82·126·126） topology which represents a rare 2-fold interpenetrating 3D framework topology network. The luminescence analyses reveal that polymer 1 shows obvious emission at room temperature in the solid state. In addition,it was also characterized by elemental,IR spectra and TG analyses.
基金This project was supported by the National Foundation for Science of China(No.U180411457)Foundation for Science&Technology Innovation Talents in Henan province(No.16410010012)the Foundation of Education Committee of Henan province(No.182102310897)
文摘A novel heteronuclear metal organic framework(MOF) incorporating both transition and alkali metal ions, namely, {(Ni_2K_2L_2·bipy]×6 H_2O]×2 H_2O}n(1, L = N-phosphonomethyl amino diacetic acid, bipy = 4,4?-dipyridine) has been obtained. Its structure was established by single-crystal X-ray diffraction analysis and further characterized by elemental analysis and IR spectroscopy. The complex crystallizes in orthorhombic system, space group Pccn with a = 14.650(11), b = 36.56(3), c = 7.112(5) ? and V = 3809.3(8) ?~3. In this framework, bipy connects adjacent Ni–K heteronuclear coordination units into 1 D railway type chains, which are further propagated into 2 D deck-like array bearing large tunnels through the carboxylic oxygen from N-phosphonomethyl amino diacetic acid. The molar electrical conductivity of heteronuclear complex increases gradually with increasing the temperature. Complex 1 also exhibits strong photoluminescent emission in the visible region.
基金supported by the National Natural Science Foundation of China (Grant No. 10604045)the University Science and Technology Planning Program of Shandong Province of China (Grant No. J09LA02)
文摘The photodetachment of a hetero-nuclear diatomic molecular negative ion is studied by using a two-centre model. An analytic formula is presented for the electron flux distribution of a heteronuclear diatomic molecular negative ion. Taking HF- as an example, we calculated the electron flux distributions of this ion for various detached electron energies. The results show that the electron flux distributions exhibit oscillatory structures, which are caused by the interference effect between the two nuclei. Besides, the laser light polarization also has a great influence on the electron flux distribution. The oscillation amplitude is the largest when the laser polarization is parallel to the z-axis; when the laser polarization is perpendicular to the z-axis, the oscillation almost vanishes. This study provides a new understanding of the photodetachment of a heteronuclear diatomic molecular negative ion.
基金We are grateful to the National Natural Science Foundation of China(project 20072034)the Natural Science Foundation of Henan province and the Foundation for Young Teacher in Zhenzhou University for the financial support.
文摘A new hetero-six-nuclear cluster was synthesized and determined by X-ray diffraction technique. The four-carboxylate groups are bound to the Cu(II) atoms to form Cu(OR)4Cu paddle-wheel-type cage between two DMF as the basis for the cluster. The distance of two copper(II) atoms is 2.642 ?, and they are bridged by the carboxylate groups. A huge system plane was auto-assembled by four host molecules and two Cu (II) ions, which was observed in the crystal structure.
