One novel metal-organic framework(MOF), [Ba(L)(HO)](1, HL =aniline-2,5-disulfonic acid), has been synthesized by hydrothermal method. Each barium atom is eleven-coordinated into a distorted monocapped pentagonal antip...One novel metal-organic framework(MOF), [Ba(L)(HO)](1, HL =aniline-2,5-disulfonic acid), has been synthesized by hydrothermal method. Each barium atom is eleven-coordinated into a distorted monocapped pentagonal antiprismatic arrangement. Compound 1 shows an interesting 3 D pillar-layered structure constructed from 2 D inorganic layers[Ba(SO)(HO)]and organic pillars of phenyl moieties of L2-linkages. The inorganic layers are supported by the organic pillars, generating a novel 3 D open framework structure with {3, 4~6, 5~5, 6~5,7~4}2{3}{5} topology. The result of fluorescence measurement can reveal that the decayed emission band centered at 492 nm may be caused by the interactions of the ligands and the metal ions.Compound 1 exhibits selective toward the adsorption of COover Nat 273 K.展开更多
A three-dimensional(3D) lanthanide metal-organic coordination polymer with a three-dimensional open framework,Tm(BTC)(DMF)(DMSO),was synthesized by reaction of the lanthanide ions(Tm3+) with 1, 3,5-benzenetricarboxyli...A three-dimensional(3D) lanthanide metal-organic coordination polymer with a three-dimensional open framework,Tm(BTC)(DMF)(DMSO),was synthesized by reaction of the lanthanide ions(Tm3+) with 1, 3,5-benzenetricarboxylic acid(H3BTC) in a mixed solution of DMF(N,N′dimethylformamide) and DMSO(dimethyl sulphoxide).This compound crystallizes in a monoclinic space group P21/n with unit cell parameters a=1.0801(2) nm,b=1.5550(3) nm,c=1.0906(2) nm,β=100.401°,V=1.8017(6) nm3 and Z=4.The compound exhibits one-dimensional channels along the direction and could uptake carbon dioxide at 1×105 Pa.展开更多
The blue-light-excitable phosphors play a crucial role in the high-performance white LEDs. Here, we report on two new Cu(Ⅰ) coordination network materials as yellow-emitting phosphors prepared by suitably expanded π...The blue-light-excitable phosphors play a crucial role in the high-performance white LEDs. Here, we report on two new Cu(Ⅰ) coordination network materials as yellow-emitting phosphors prepared by suitably expanded π-conjugated triazole ligands. Upon blue-light irradiation, these complexes exhibit efficient solid-state emission and enhanced photostability. Through incorporating the yellow phosphor and a commercial blue-green powder(BaSi_(2)N_(2)O_(2):Eu^(2+)) with a blue LED chip, the phosphor-converted LED devices display remarkable white emission properties. The experimental results demonstrate that the Cu(Ⅰ)coordination network materials function as promising blue-light excitable phosphors with great application potential for full-spectrum white LEDs.展开更多
Solvothermal reactions of 1,3,5-benzenetricarboxylic acid (H3btc) with cadmium acetate or zinc acetate yielded two compounds formulated as (Me2NH2)[Cd(btc)]·DMA (1) (btc = 1,3,5-benzenetricarboxylate, DMA = N,N-d...Solvothermal reactions of 1,3,5-benzenetricarboxylic acid (H3btc) with cadmium acetate or zinc acetate yielded two compounds formulated as (Me2NH2)[Cd(btc)]·DMA (1) (btc = 1,3,5-benzenetricarboxylate, DMA = N,N-dimethylacetamide) and (Me2NH2)[Zn(btc)]·DMF (2) (DMF = N,N-dimethylformamide). Both are 3-D frameworks with the rutile topology, which are constructed from six-connected dimeric metal cores and three-connected btc linkers. The solvent molecules and counter cations are located in the 1-D channels of the frameworks. A slight difference between the two compounds is the different connectivity modes of the metal atoms with the carboxylate groups of the ligands. However, this slight difference results in distinct flexibilities of the two frameworks. Variable-temperature powder X-ray diffraction studies revealed that the framework of 1 collapses when heated at 180 °C with loss of the guest species, but compound 2 undergoes two structural transformations below 380 °C. Thermogravimetry-infrared spectroscopy analysis for 2 showed that the two structural transformations are induced by separate losses of solvent molecules and counter cations, and that the dimethylammonium cations are eliminated as neutral dimethylamine molecules. IR spectroscopy demonstrated that the protons are transferred from the counter cations onto the uncoordinated carboxylate oxygen atoms on the channel walls. Sorption and proton conduction studies have also been performed for the compounds.展开更多
（E）-2,6-Dimethyl-4-styrylpyridine-3,5-dicarboxylic acid （H2mspda） is firstly employed in coordination chemistry.Two isostructural two-dimensional （2-D） 4-connected metal-organic coordination polymers with a gene...（E）-2,6-Dimethyl-4-styrylpyridine-3,5-dicarboxylic acid （H2mspda） is firstly employed in coordination chemistry.Two isostructural two-dimensional （2-D） 4-connected metal-organic coordination polymers with a general formula of {M2[（mspda）2（bpy）（H2O）2]}n （M=Zn（1） and Co（2）） are assembled from H2mspda,4,4＇-bipyridyl （bpy）,zinc and cobalt ions under hydrothermal conditions,and characterized by single-crystal X-ray diffraction analyses.Complex 1 crystallizes in monoclinic,space group P21/n with a=14.551（4）,b=10.941（3）,c=14.945（4）,β=98.817（4）o,V=2351.3（1）3,Dc=1.511 g/cm3,μ（MoKα）=1.090 mm-1,F（000）=1104,Z=4,the final R=0.0335 and wR=0.0485 for 3296 observed reflections （I 〉 2σ（I））.In compound 1,mspda2-spacers are only arrayed in a head-to-tail fashion which corresponds to a 2-D coordination polymer.Solid-state H2mspda and complex 1 have expected photoluminescence （λem=475～496 nm） at room temperature.展开更多
A new mellitate complex [Cu3（μ2-mellitate）（μ2-H2O）（H2O）2·H2O]n 1 has been synthesized by the reaction of mellitic acid and Cu（CH3COO）2·H2O in the presence of base. Crystallographic data for 1： C12...A new mellitate complex [Cu3（μ2-mellitate）（μ2-H2O）（H2O）2·H2O]n 1 has been synthesized by the reaction of mellitic acid and Cu（CH3COO）2·H2O in the presence of base. Crystallographic data for 1： C12H8O16Cu3, Mr = 598.80, orthorhombic, Pbcn, a = 8.4378（6）, b = 10.0396（7）, c = 17.6799（12）A, V = 1497.70（18）A^3, Z = 4, De = 2.656 g/cm^3, μ = 4.327 mm^-1, F（000） = 1180, R = 0.0431 and wR = 0.0964 for 1075 observed reflections （I 〉 2σ（I））. X-ray crystal structural analysis revealed that the mellitate anions behave as the bridging ligands and link eight copper atoms repeatedly to form a novel three-dimensional metal-organic coordination polymer with two different rhombic tunnels in the solid-state structure.展开更多
基金supported by the Liaoning Provincial Education Department(No.L2015299)Innovative training program for College Students(Nos.201710148000118,201710148000147)
文摘One novel metal-organic framework(MOF), [Ba(L)(HO)](1, HL =aniline-2,5-disulfonic acid), has been synthesized by hydrothermal method. Each barium atom is eleven-coordinated into a distorted monocapped pentagonal antiprismatic arrangement. Compound 1 shows an interesting 3 D pillar-layered structure constructed from 2 D inorganic layers[Ba(SO)(HO)]and organic pillars of phenyl moieties of L2-linkages. The inorganic layers are supported by the organic pillars, generating a novel 3 D open framework structure with {3, 4~6, 5~5, 6~5,7~4}2{3}{5} topology. The result of fluorescence measurement can reveal that the decayed emission band centered at 492 nm may be caused by the interactions of the ligands and the metal ions.Compound 1 exhibits selective toward the adsorption of COover Nat 273 K.
文摘A three-dimensional(3D) lanthanide metal-organic coordination polymer with a three-dimensional open framework,Tm(BTC)(DMF)(DMSO),was synthesized by reaction of the lanthanide ions(Tm3+) with 1, 3,5-benzenetricarboxylic acid(H3BTC) in a mixed solution of DMF(N,N′dimethylformamide) and DMSO(dimethyl sulphoxide).This compound crystallizes in a monoclinic space group P21/n with unit cell parameters a=1.0801(2) nm,b=1.5550(3) nm,c=1.0906(2) nm,β=100.401°,V=1.8017(6) nm3 and Z=4.The compound exhibits one-dimensional channels along the direction and could uptake carbon dioxide at 1×105 Pa.
基金supported by the National Natural Science Foundation of China (No.92161121)。
文摘The blue-light-excitable phosphors play a crucial role in the high-performance white LEDs. Here, we report on two new Cu(Ⅰ) coordination network materials as yellow-emitting phosphors prepared by suitably expanded π-conjugated triazole ligands. Upon blue-light irradiation, these complexes exhibit efficient solid-state emission and enhanced photostability. Through incorporating the yellow phosphor and a commercial blue-green powder(BaSi_(2)N_(2)O_(2):Eu^(2+)) with a blue LED chip, the phosphor-converted LED devices display remarkable white emission properties. The experimental results demonstrate that the Cu(Ⅰ)coordination network materials function as promising blue-light excitable phosphors with great application potential for full-spectrum white LEDs.
基金supported by the National Natural Science Foundation of China (20821001 & 90922031)the National Basic Research Program of China (2007CB815302)the Open Fund of the State Key Laboratory of Optoelectronic Materials and Technologies
文摘Solvothermal reactions of 1,3,5-benzenetricarboxylic acid (H3btc) with cadmium acetate or zinc acetate yielded two compounds formulated as (Me2NH2)[Cd(btc)]·DMA (1) (btc = 1,3,5-benzenetricarboxylate, DMA = N,N-dimethylacetamide) and (Me2NH2)[Zn(btc)]·DMF (2) (DMF = N,N-dimethylformamide). Both are 3-D frameworks with the rutile topology, which are constructed from six-connected dimeric metal cores and three-connected btc linkers. The solvent molecules and counter cations are located in the 1-D channels of the frameworks. A slight difference between the two compounds is the different connectivity modes of the metal atoms with the carboxylate groups of the ligands. However, this slight difference results in distinct flexibilities of the two frameworks. Variable-temperature powder X-ray diffraction studies revealed that the framework of 1 collapses when heated at 180 °C with loss of the guest species, but compound 2 undergoes two structural transformations below 380 °C. Thermogravimetry-infrared spectroscopy analysis for 2 showed that the two structural transformations are induced by separate losses of solvent molecules and counter cations, and that the dimethylammonium cations are eliminated as neutral dimethylamine molecules. IR spectroscopy demonstrated that the protons are transferred from the counter cations onto the uncoordinated carboxylate oxygen atoms on the channel walls. Sorption and proton conduction studies have also been performed for the compounds.
基金National Natural Science Foundation of China(50730003,50672025,20806024,and 51002051)Fundamental Research Funds for the Central Universities(WA1014016)Research Fund of China 863 program(2008AA062302)~~
基金Supported by the Key Project of Chinese Ministry of Education (No. 208116)the Scientific and Technological Project of CQEC (No. KJ080829)
文摘（E）-2,6-Dimethyl-4-styrylpyridine-3,5-dicarboxylic acid （H2mspda） is firstly employed in coordination chemistry.Two isostructural two-dimensional （2-D） 4-connected metal-organic coordination polymers with a general formula of {M2[（mspda）2（bpy）（H2O）2]}n （M=Zn（1） and Co（2）） are assembled from H2mspda,4,4＇-bipyridyl （bpy）,zinc and cobalt ions under hydrothermal conditions,and characterized by single-crystal X-ray diffraction analyses.Complex 1 crystallizes in monoclinic,space group P21/n with a=14.551（4）,b=10.941（3）,c=14.945（4）,β=98.817（4）o,V=2351.3（1）3,Dc=1.511 g/cm3,μ（MoKα）=1.090 mm-1,F（000）=1104,Z=4,the final R=0.0335 and wR=0.0485 for 3296 observed reflections （I 〉 2σ（I））.In compound 1,mspda2-spacers are only arrayed in a head-to-tail fashion which corresponds to a 2-D coordination polymer.Solid-state H2mspda and complex 1 have expected photoluminescence （λem=475～496 nm） at room temperature.
基金the State Key Basic Research and Development Plan of China (001CB108906)the Knowledge Innovation Program of the Chinese Academy of Sciences, the NSF (E0620005)+1 种基金the Major Special Foundation of Fujian Province (2005HZ1027, 2005HZ01-1)the Natural Science Foundation of Fujian Province (2006F3042)
文摘A new mellitate complex [Cu3（μ2-mellitate）（μ2-H2O）（H2O）2·H2O]n 1 has been synthesized by the reaction of mellitic acid and Cu（CH3COO）2·H2O in the presence of base. Crystallographic data for 1： C12H8O16Cu3, Mr = 598.80, orthorhombic, Pbcn, a = 8.4378（6）, b = 10.0396（7）, c = 17.6799（12）A, V = 1497.70（18）A^3, Z = 4, De = 2.656 g/cm^3, μ = 4.327 mm^-1, F（000） = 1180, R = 0.0431 and wR = 0.0964 for 1075 observed reflections （I 〉 2σ（I））. X-ray crystal structural analysis revealed that the mellitate anions behave as the bridging ligands and link eight copper atoms repeatedly to form a novel three-dimensional metal-organic coordination polymer with two different rhombic tunnels in the solid-state structure.
