Two crystals of receptor 1, C（42）H（52）N（10）O4S2（anthracene-9,10-dicarbaldehyde bis-（phenyl-semithiocarbazone）） and-1-H2PO4, C（68）H（114）N（10）O（10）P2S2 were obtained at room temperature successfully, a...Two crystals of receptor 1, C（42）H（52）N（10）O4S2（anthracene-9,10-dicarbaldehyde bis-（phenyl-semithiocarbazone）） and-1-H2PO4, C（68）H（114）N（10）O（10）P2S2 were obtained at room temperature successfully, and their structures were characterized by X-ray crystallography diffraction. X-ray diffraction reveals that, receptor 1 crystallizes in monoclinic, space group P21/c, with a = 9.487（3）,b = 20.674（6）, c = 11.821（4）A, β = 113.416（8）o, Mr = 825.06, V = 2127.5（12） A^3, Z = 2, Dc = 1.288g/cm^3, μ = 0.18 mm^-1, F（000） = 876, MoK α radiation（λ = 0.71073 A）, the final R = 0.0472 and wR = 0.0930. A total of 3758 unique reflections were collected, of which 3313 with I 〉 2σ（I） were observed. Compound 1-H2PO4^-crystallizes in triclinic, space group P21/n, with a = 8.767（1）, b =13.6190（15）, c = 16.615（2） ？, α = 98.727（14）, β = 103.061（14）, γ = 91.382（16）°, Mr = 1357.75, V =1906.6（4） A^3, Z = 1, Dc = 1.183 g/cm^3, μ = 0.17 mm-（-1）, F（000） = 734, MoK α radiation（λ = 0.71073？）, the final R = 0.0769 and wR = 0.1884. A total of 6699 unique reflections were collected, of which 2989 with I 〉 2σ（I） were observed. As it was observed in the crystal structure of 1-H2PO4^-, 1bound H2PO4^-at a 1：2 ratio by intermolecular interaction of N-H···O hydrogen bond obviously.Another interesting feature was that H2PO4--groups assembled chains themselves via intramolecular hydrogen bond O-H···O and connected the 1 molecules together through the interaction of H-bonds,which improved the planarity of 1 and increased the stability of the entire structure.展开更多
Three new suprarnolecular networks based on paratungstate and N-donor bridging ligands, [H2bpmp]2,5H[H2W12O40]·2H20（1）, [H2（bpp）]2[H（py-CH3）]0.25 [H（py-C2Hs）]0.25H1.5[H2W12O40]·4H2O（2） and [H2pip]3...Three new suprarnolecular networks based on paratungstate and N-donor bridging ligands, [H2bpmp]2,5H[H2W12O40]·2H20（1）, [H2（bpp）]2[H（py-CH3）]0.25 [H（py-C2Hs）]0.25H1.5[H2W12O40]·4H2O（2） and [H2pip]3[H2W12O40]（3）[bpmp=N,N＇-bis（4-pyridylmethyl）piperazine; bpp=l,3-bis（4-pyridyl）propane; py=pyridine; pip=piperazine] were prepared by the hydrothermal synthesis and characterized by elemental analysis, infrared（IR）, thermogravimetric（TG） analysis and single-crystal X-ray diffraction（XRD）. All the compounds show high-dimen- sional suprarnolecular networks based on [H2W12O40]^6- and the protonated N-donor ligands via the N-H.…O-W hydrogen bonds and/or π…πstacking interactions. Their luminescent properties were investigated.展开更多
The title complex, {[Cu2（4,4＇-bipyridine）2（μ-O2CMe）2（O2CMe）2],H2O}n 1, was synthesized and structurally characterized by X-ray crystallography. It crystallizes in monoclinic, space group C2/c with a = 13.4474...The title complex, {[Cu2（4,4＇-bipyridine）2（μ-O2CMe）2（O2CMe）2],H2O}n 1, was synthesized and structurally characterized by X-ray crystallography. It crystallizes in monoclinic, space group C2/c with a = 13.4474（5）, b = 11.7566（2）, c = 19.5380（6）A, β = 92.930（2）°, V = 3084.84（16） A^3, Z = 4, Cu2C28N409H30, Mr = 693.64, Dc = 1.494 g/cm^3, F（000） = 1424 and μ（MoKα） = 1.436 mm^-1. With the use of 2062 observed reflections （I 〉 2σ（I））, the structure was refined to R = 0.0769 and wR = 0.2154. In complex 1, the dimeric copper acetate units are linked through 4,4’-bipyridine to yield ID molecular ladders. These ladders are connected via O-H…O hydrogen bonds to generate 2D layers, which are further linked through C-H…O hydrogen bonds to give a 3D supramolecular network.展开更多
A new compound [Zn3（C7NO4H3）3Cl4]·[C6NO2H6]4·4H2O （I） has been synthesized and structurally characterized by X-ray crystallography.It crystallizes in monoclinic,space group C2/c with a=16.9018（14）,b=12...A new compound [Zn3（C7NO4H3）3Cl4]·[C6NO2H6]4·4H2O （I） has been synthesized and structurally characterized by X-ray crystallography.It crystallizes in monoclinic,space group C2/c with a=16.9018（14）,b=12.6902（10）,c=25.1170（2）,β=90.54°,V=5387.0（8）3,Z=4,Zn3C45H41Cl4N7O24,Mr=1401.76,Dc=1.728 g/cm3,F（000）=2840,μ（MoKa）=1.615 mm-1,the R= 0.0758 and wR=0.2060 for 3468 observed reflections （I 〉 2σ（I））.Analysis of single-crystal X-ray diffraction data shows that compound I displays an interesting example of 3D supramolecular networks with perfect neutral and ionic hydrogen bonding array.展开更多
In this review a series of organic-based open porous networks are discussed, in which hydrogen bonds play an important role in network formation. Using these open networks as molecular templates: 1) a wealth of functi...In this review a series of organic-based open porous networks are discussed, in which hydrogen bonds play an important role in network formation. Using these open networks as molecular templates: 1) a wealth of functional guest species can be immo- bilized; 2) fullerene molecules can be separated and recognized; 3) photoisomerization reactions can be observed by STM; 4) 1D molecular arrays can be constructed; and 5) heterogeneous bilayer structures can be formed. It is envisioned that these su- pramolecular networks might be developed into a new family of useful soft frameworks for studies toward shape-selective ca- talysis, molecular recognition and host-guest supramolecular chemistry.展开更多
A novel compound (NH4)2Y(H2O)8[PMo10V2O40]·10H2O has been prepared in an aqueous solution and characterized by elemental analysis, IR, and TG-DTG analysis. X-ray diffraction analysis was carried out on (NH4)2Y(H2...A novel compound (NH4)2Y(H2O)8[PMo10V2O40]·10H2O has been prepared in an aqueous solution and characterized by elemental analysis, IR, and TG-DTG analysis. X-ray diffraction analysis was carried out on (NH4)2Y(H2O)8 [PMo10V2O40]·10H2O single crystal, which crystallizes in the monoclinic system of a space group P21/c with a=0.9871(3) nm,b=1.5424(5) nm, c=2.7924(9) nm, β= 94.183(5)° and Z=2. In the compound, a two-dimensional network is constructed by the PMo10V2O54-0 anion and the Y(H2O)83+ cation building blocks via hydrogen bonding exhibiting the porous structure.展开更多
A simple and general strategy is described for preparing network supported catalyst through a one-pot synthetic procedure using supramolecular gel as template.This procedure directly attaches ligand to support during ...A simple and general strategy is described for preparing network supported catalyst through a one-pot synthetic procedure using supramolecular gel as template.This procedure directly attaches ligand to support during fabricating the support.Using this strategy,supported CuBr/di-（2-picolyl） amine catalyst with U-shaped fibrillar network was prepared and used in atom transfer radical polymerization of methyl methacrylate.XPS and SEM characterization of the catalyst revealed homogeneous distribution of ligand,sufficient reactive sites,adequate mechanical strength and macroporosity.The polymerization results demonstrated high activity and reusability of such catalyst.This strategy might be extended to other supported catalysts used in column reactors.展开更多
The title compounds, [Co（H2O）6]（OVA）2·2H2O 1, [Ni（H2O）6]（OVA）2·2H2O 2 and [Zn（OVA）2·2H2O] 3 （HOVA = o-vanillic acid = 2-hydroxy-3-methoxybenzoate）, were synthesized and characterized by sing...The title compounds, [Co（H2O）6]（OVA）2·2H2O 1, [Ni（H2O）6]（OVA）2·2H2O 2 and [Zn（OVA）2·2H2O] 3 （HOVA = o-vanillic acid = 2-hydroxy-3-methoxybenzoate）, were synthesized and characterized by single-crystal X-ray diffraction, elemental analysis, IR and TGA. Compounds 1 and 2 are both of triclinic with space group P1. The metal atom coordinated by six water molecules displays a slightly distorted octahedral configuration. Interestingly, the carboxyl group from HOVA ligand does not coordinate to the metal atom. Correspondingly, compound 3 belongs to the monoclinic system, space group C2/c. Each zinc（Ⅱ） atom exhibits a distorted four-coordinated tetrahedral geometry. Two monodentate carboxyl groups link one zinc（Ⅱ） atom to form a mononuclear molecule. The structure feature is different from that of compounds 1 and 2, which could be attributed to the different coordinated numbers and radii of Co（Ⅱ）, Ni（Ⅱ） and Zn（Ⅱ） atoms.展开更多
A new bis（imidazolium） compound,[H2L（H2btec）2]·H4btec（1,L=1,1＇-（butane-1,4-diyl）bis（imidazole）,H4btec=1,2,4,5-benzenetetracarboxylatic acid）,has been synthesized and structurally characterized by singl...A new bis（imidazolium） compound,[H2L（H2btec）2]·H4btec（1,L=1,1＇-（butane-1,4-diyl）bis（imidazole）,H4btec=1,2,4,5-benzenetetracarboxylatic acid）,has been synthesized and structurally characterized by single-crystal X-ray diffraction.The title compound crystallizes in the monoclinic system,space group Pnma,with a=13.3908（11）,b=13.9249（12）,c=16.2166（14）,V=2957.6（4）3,Z=4,Mr=698.55,Dc=1.569 mg/m3,F（000）=1448,μ（MoKα）=0.130 mm-1,the final R=0.0584 and wR=0.1538 for 4295 observed reflections with I2σ（I）.The compound consists of one 1,1＇-（butane-1,4-diyl）bis（imidazolium） cation,one neutral H4btec and one H2btec2-（Only two para carboxyl groups are deprotonated,and two protonated ones remain free） anion.A one-dimensional hydrogen bonding chain and a 2D hydrogen bonding network are formed via intermolecular N–H…O and O–H…O hydrogen bonds.These adjacent chains are further stacked through intermolecular π-π and hydrogen bonding interactions to form a 3D supramolecular network.展开更多
A new cobalt compound,{[Co（H2btec）（2,2＇-bipy）（H2O）3]·H2O}n （1,H4btec=1,2,4,5-benzenetetracarboxylic acid,2,2＇-bipy=2,2＇-bipyridine）,has been synthesized and charac-terized by single-crystal X-ray diffr...A new cobalt compound,{[Co（H2btec）（2,2＇-bipy）（H2O）3]·H2O}n （1,H4btec=1,2,4,5-benzenetetracarboxylic acid,2,2＇-bipy=2,2＇-bipyridine）,has been synthesized and charac-terized by single-crystal X-ray diffraction,elemental analysis,IR and X-ray powder diffraction.The crystal belongs to the triclinic system,space group P1,with a=7.230（3）,b=11.626（5）,c=14.001（6）,α=108.12（0）°,β=95.85（0）°,V=1095.33（157）3,C20H20CoN2O12,Mr=539.31,Z= 2,Dc=1.635 g/cm3,μ=0.855 mm-1,F（000）=554,R=0.0427 and wR=0.1042 for 3883 observed reflections （I 〉 2σ（I））.The title compound features a discrete molecular structure,which is connected with each other through extensive O-H…O hydrogen bonds into an intricate 3D supramolecular network.Additionally,two different patterns of π-π stacking interactions further consolidate the framework.展开更多
A one-dimensional （1D） supramolecular rare earth complex [Nd（NO3）2L2-（C3H6O）][NdL（NO3）4]} （L=N-（6-（4-methylpyridinyl））ketoacetamide） has been prepared and characterized by elemental analysis, IR and elec...A one-dimensional （1D） supramolecular rare earth complex [Nd（NO3）2L2-（C3H6O）][NdL（NO3）4]} （L=N-（6-（4-methylpyridinyl））ketoacetamide） has been prepared and characterized by elemental analysis, IR and electronic spectroscopy, and single-crystal X-ray diffraction. The crystal crystallizes in the triclinic system, space group P1^- with a=0.9146（6）, b=1.2581（8）, c=2.2316（14） nm, α=99.352（10）,β=97.209（9）, γ=103.935（9）°, V=2.422（3） nm3, Dc=1.776 g/cm^3, C33H42N12Nd2O25, Mr=1295.27, Z=2, F（000）=1288, μ=2.217 mm-1, R=0.0508and wR=0.1046 for 5173 observed reflections （I 〉 2σ（I））. In the structure of the title complex,one-dimensional supramolecular double-chains are formed by intermolecular hydrogen bonding interactions.展开更多
A novel coordination polymers [Cu2（ETU）6]SO4（1）（ETU=ethylidene thiourea） was synthesized under solvothermal conditions.The crystal structure of the polymer was determined by X-ray diffraction: trigonal,space gro...A novel coordination polymers [Cu2（ETU）6]SO4（1）（ETU=ethylidene thiourea） was synthesized under solvothermal conditions.The crystal structure of the polymer was determined by X-ray diffraction: trigonal,space group R3c（No.161）,a=1.275 09（8） nm,b=1.275 09（8） nm,c=3.574 7（7） nm,γ=120°,Z=6,CCDC Number: 605501.In the structure of the polymer,each metal ion Cu（Ⅰ） coordinates to three S atoms attached to the ring of ETU forming two triangular pinwheel-shape monovalent cations[Cu2（ETU）6]+, in one of which the counter-ion SO2-4 is located.The ions with contrary charge,[Cu2（ETU）6]+ and SO2-4,are held together via the N—H…O hydrogen-bonded interactions resulting in a three-dimensional supramolecular network.展开更多
基金supported by the China Postdoctoral Science Foundation(No.2014M551053)Natural Science Foundation of Hebei Province(No.B2015203124)Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education),Nankai University
文摘Two crystals of receptor 1, C（42）H（52）N（10）O4S2（anthracene-9,10-dicarbaldehyde bis-（phenyl-semithiocarbazone）） and-1-H2PO4, C（68）H（114）N（10）O（10）P2S2 were obtained at room temperature successfully, and their structures were characterized by X-ray crystallography diffraction. X-ray diffraction reveals that, receptor 1 crystallizes in monoclinic, space group P21/c, with a = 9.487（3）,b = 20.674（6）, c = 11.821（4）A, β = 113.416（8）o, Mr = 825.06, V = 2127.5（12） A^3, Z = 2, Dc = 1.288g/cm^3, μ = 0.18 mm^-1, F（000） = 876, MoK α radiation（λ = 0.71073 A）, the final R = 0.0472 and wR = 0.0930. A total of 3758 unique reflections were collected, of which 3313 with I 〉 2σ（I） were observed. Compound 1-H2PO4^-crystallizes in triclinic, space group P21/n, with a = 8.767（1）, b =13.6190（15）, c = 16.615（2） ？, α = 98.727（14）, β = 103.061（14）, γ = 91.382（16）°, Mr = 1357.75, V =1906.6（4） A^3, Z = 1, Dc = 1.183 g/cm^3, μ = 0.17 mm-（-1）, F（000） = 734, MoK α radiation（λ = 0.71073？）, the final R = 0.0769 and wR = 0.1884. A total of 6699 unique reflections were collected, of which 2989 with I 〉 2σ（I） were observed. As it was observed in the crystal structure of 1-H2PO4^-, 1bound H2PO4^-at a 1：2 ratio by intermolecular interaction of N-H···O hydrogen bond obviously.Another interesting feature was that H2PO4--groups assembled chains themselves via intramolecular hydrogen bond O-H···O and connected the 1 molecules together through the interaction of H-bonds,which improved the planarity of 1 and increased the stability of the entire structure.
基金Supported by the National Natural Science Foundation of China(No.91027002)the Fundamental Research Funds for the Central Universities,China(No.11CXPY002)
文摘Three new suprarnolecular networks based on paratungstate and N-donor bridging ligands, [H2bpmp]2,5H[H2W12O40]·2H20（1）, [H2（bpp）]2[H（py-CH3）]0.25 [H（py-C2Hs）]0.25H1.5[H2W12O40]·4H2O（2） and [H2pip]3[H2W12O40]（3）[bpmp=N,N＇-bis（4-pyridylmethyl）piperazine; bpp=l,3-bis（4-pyridyl）propane; py=pyridine; pip=piperazine] were prepared by the hydrothermal synthesis and characterized by elemental analysis, infrared（IR）, thermogravimetric（TG） analysis and single-crystal X-ray diffraction（XRD）. All the compounds show high-dimen- sional suprarnolecular networks based on [H2W12O40]^6- and the protonated N-donor ligands via the N-H.…O-W hydrogen bonds and/or π…πstacking interactions. Their luminescent properties were investigated.
基金This work was supported by the Science Foundation of Fujian Provincial Key Laboratory of Polymer Materials
文摘The title complex, {[Cu2（4,4＇-bipyridine）2（μ-O2CMe）2（O2CMe）2],H2O}n 1, was synthesized and structurally characterized by X-ray crystallography. It crystallizes in monoclinic, space group C2/c with a = 13.4474（5）, b = 11.7566（2）, c = 19.5380（6）A, β = 92.930（2）°, V = 3084.84（16） A^3, Z = 4, Cu2C28N409H30, Mr = 693.64, Dc = 1.494 g/cm^3, F（000） = 1424 and μ（MoKα） = 1.436 mm^-1. With the use of 2062 observed reflections （I 〉 2σ（I））, the structure was refined to R = 0.0769 and wR = 0.2154. In complex 1, the dimeric copper acetate units are linked through 4,4’-bipyridine to yield ID molecular ladders. These ladders are connected via O-H…O hydrogen bonds to generate 2D layers, which are further linked through C-H…O hydrogen bonds to give a 3D supramolecular network.
基金supported by the Natural Science Foundation of Fujian Province (2006F3042)
文摘A new compound [Zn3（C7NO4H3）3Cl4]·[C6NO2H6]4·4H2O （I） has been synthesized and structurally characterized by X-ray crystallography.It crystallizes in monoclinic,space group C2/c with a=16.9018（14）,b=12.6902（10）,c=25.1170（2）,β=90.54°,V=5387.0（8）3,Z=4,Zn3C45H41Cl4N7O24,Mr=1401.76,Dc=1.728 g/cm3,F（000）=2840,μ（MoKa）=1.615 mm-1,the R= 0.0758 and wR=0.2060 for 3468 observed reflections （I 〉 2σ（I））.Analysis of single-crystal X-ray diffraction data shows that compound I displays an interesting example of 3D supramolecular networks with perfect neutral and ionic hydrogen bonding array.
文摘In this review a series of organic-based open porous networks are discussed, in which hydrogen bonds play an important role in network formation. Using these open networks as molecular templates: 1) a wealth of functional guest species can be immo- bilized; 2) fullerene molecules can be separated and recognized; 3) photoisomerization reactions can be observed by STM; 4) 1D molecular arrays can be constructed; and 5) heterogeneous bilayer structures can be formed. It is envisioned that these su- pramolecular networks might be developed into a new family of useful soft frameworks for studies toward shape-selective ca- talysis, molecular recognition and host-guest supramolecular chemistry.
文摘A novel compound (NH4)2Y(H2O)8[PMo10V2O40]·10H2O has been prepared in an aqueous solution and characterized by elemental analysis, IR, and TG-DTG analysis. X-ray diffraction analysis was carried out on (NH4)2Y(H2O)8 [PMo10V2O40]·10H2O single crystal, which crystallizes in the monoclinic system of a space group P21/c with a=0.9871(3) nm,b=1.5424(5) nm, c=2.7924(9) nm, β= 94.183(5)° and Z=2. In the compound, a two-dimensional network is constructed by the PMo10V2O54-0 anion and the Y(H2O)83+ cation building blocks via hydrogen bonding exhibiting the porous structure.
基金support from the National Natural Science Foundation of China(Nos.20574041 and 20874055)Hi-tech Research and Development Program(863 plan) of China(No.2009AA062903)
文摘A simple and general strategy is described for preparing network supported catalyst through a one-pot synthetic procedure using supramolecular gel as template.This procedure directly attaches ligand to support during fabricating the support.Using this strategy,supported CuBr/di-（2-picolyl） amine catalyst with U-shaped fibrillar network was prepared and used in atom transfer radical polymerization of methyl methacrylate.XPS and SEM characterization of the catalyst revealed homogeneous distribution of ligand,sufficient reactive sites,adequate mechanical strength and macroporosity.The polymerization results demonstrated high activity and reusability of such catalyst.This strategy might be extended to other supported catalysts used in column reactors.
基金supported by the National Natural Science Foundation of China (No. 20573073)the Natural Scientific Research Foundation of Shaanxi Provincial Education Office of China (No. 09JK826, 08JZ82 and 08JK490)
文摘The title compounds, [Co（H2O）6]（OVA）2·2H2O 1, [Ni（H2O）6]（OVA）2·2H2O 2 and [Zn（OVA）2·2H2O] 3 （HOVA = o-vanillic acid = 2-hydroxy-3-methoxybenzoate）, were synthesized and characterized by single-crystal X-ray diffraction, elemental analysis, IR and TGA. Compounds 1 and 2 are both of triclinic with space group P1. The metal atom coordinated by six water molecules displays a slightly distorted octahedral configuration. Interestingly, the carboxyl group from HOVA ligand does not coordinate to the metal atom. Correspondingly, compound 3 belongs to the monoclinic system, space group C2/c. Each zinc（Ⅱ） atom exhibits a distorted four-coordinated tetrahedral geometry. Two monodentate carboxyl groups link one zinc（Ⅱ） atom to form a mononuclear molecule. The structure feature is different from that of compounds 1 and 2, which could be attributed to the different coordinated numbers and radii of Co（Ⅱ）, Ni（Ⅱ） and Zn（Ⅱ） atoms.
基金supported by the Natural Science Foundation of Henan Province (No 092102310075)
文摘A new bis（imidazolium） compound,[H2L（H2btec）2]·H4btec（1,L=1,1＇-（butane-1,4-diyl）bis（imidazole）,H4btec=1,2,4,5-benzenetetracarboxylatic acid）,has been synthesized and structurally characterized by single-crystal X-ray diffraction.The title compound crystallizes in the monoclinic system,space group Pnma,with a=13.3908（11）,b=13.9249（12）,c=16.2166（14）,V=2957.6（4）3,Z=4,Mr=698.55,Dc=1.569 mg/m3,F（000）=1448,μ（MoKα）=0.130 mm-1,the final R=0.0584 and wR=0.1538 for 4295 observed reflections with I2σ（I）.The compound consists of one 1,1＇-（butane-1,4-diyl）bis（imidazolium） cation,one neutral H4btec and one H2btec2-（Only two para carboxyl groups are deprotonated,and two protonated ones remain free） anion.A one-dimensional hydrogen bonding chain and a 2D hydrogen bonding network are formed via intermolecular N–H…O and O–H…O hydrogen bonds.These adjacent chains are further stacked through intermolecular π-π and hydrogen bonding interactions to form a 3D supramolecular network.
基金supported by 973 Program (2007CB815302,2009CB939803)Chinese Academy of Sciences (KJCX2.YW.319,KJCX2.YW.M10,KJCX2-YW-M05)the Knowledge Innovation Program of Chinese Academy of Science,and Fujian Key Laboratory of Nanomaterials (2006L2005)
文摘A new cobalt compound,{[Co（H2btec）（2,2＇-bipy）（H2O）3]·H2O}n （1,H4btec=1,2,4,5-benzenetetracarboxylic acid,2,2＇-bipy=2,2＇-bipyridine）,has been synthesized and charac-terized by single-crystal X-ray diffraction,elemental analysis,IR and X-ray powder diffraction.The crystal belongs to the triclinic system,space group P1,with a=7.230（3）,b=11.626（5）,c=14.001（6）,α=108.12（0）°,β=95.85（0）°,V=1095.33（157）3,C20H20CoN2O12,Mr=539.31,Z= 2,Dc=1.635 g/cm3,μ=0.855 mm-1,F（000）=554,R=0.0427 and wR=0.1042 for 3883 observed reflections （I 〉 2σ（I））.The title compound features a discrete molecular structure,which is connected with each other through extensive O-H…O hydrogen bonds into an intricate 3D supramolecular network.Additionally,two different patterns of π-π stacking interactions further consolidate the framework.
基金This work was supported by the National Natural Science Foundation of China (No. 20401008)
文摘A one-dimensional （1D） supramolecular rare earth complex [Nd（NO3）2L2-（C3H6O）][NdL（NO3）4]} （L=N-（6-（4-methylpyridinyl））ketoacetamide） has been prepared and characterized by elemental analysis, IR and electronic spectroscopy, and single-crystal X-ray diffraction. The crystal crystallizes in the triclinic system, space group P1^- with a=0.9146（6）, b=1.2581（8）, c=2.2316（14） nm, α=99.352（10）,β=97.209（9）, γ=103.935（9）°, V=2.422（3） nm3, Dc=1.776 g/cm^3, C33H42N12Nd2O25, Mr=1295.27, Z=2, F（000）=1288, μ=2.217 mm-1, R=0.0508and wR=0.1046 for 5173 observed reflections （I 〉 2σ（I））. In the structure of the title complex,one-dimensional supramolecular double-chains are formed by intermolecular hydrogen bonding interactions.
文摘A novel coordination polymers [Cu2（ETU）6]SO4（1）（ETU=ethylidene thiourea） was synthesized under solvothermal conditions.The crystal structure of the polymer was determined by X-ray diffraction: trigonal,space group R3c（No.161）,a=1.275 09（8） nm,b=1.275 09（8） nm,c=3.574 7（7） nm,γ=120°,Z=6,CCDC Number: 605501.In the structure of the polymer,each metal ion Cu（Ⅰ） coordinates to three S atoms attached to the ring of ETU forming two triangular pinwheel-shape monovalent cations[Cu2（ETU）6]+, in one of which the counter-ion SO2-4 is located.The ions with contrary charge,[Cu2（ETU）6]+ and SO2-4,are held together via the N—H…O hydrogen-bonded interactions resulting in a three-dimensional supramolecular network.
