A new cadmium（Ⅱ） polymer [Cd（tdc）（Phen）]n 1 （H2tdc = thiophene-3,4-dicar-boxylic acid, Phen = 1,10-phenanthroline） was synthesized under hydrothermal conditions. The compound crystallizes in the triclinic sys...A new cadmium（Ⅱ） polymer [Cd（tdc）（Phen）]n 1 （H2tdc = thiophene-3,4-dicar-boxylic acid, Phen = 1,10-phenanthroline） was synthesized under hydrothermal conditions. The compound crystallizes in the triclinic system, space group P , with a = 7.3150（10）, b = 10.3598（14）, c = 10.8784（15） , α = 82.2740（10）, β = 72.9730（10）, γ = 80.236（2）°, V = 773.68（18） 3, Z = 2, Mr = 462.74, Dc = 1.986 Mg/m3, μ = 1.58 mm-1, F（000） = 456, the final R = 0.0218 and wR = 0.0465 for 3361 observed reflections with Ⅰ 〉 2σ（Ⅰ）. The compound presents a one-dimensional （1-D） double-stranded structure and exhibits fluorescent emission at room temperature. Furthermore, infrared spectroscopy, elemental analyses, thermogravimetric analysis and powder X-ray diffraction properties of the compound are also investigated.展开更多
The reaction of L-histidine, CdCl22.5H2O and 4,4-bipyridine in methane/water gave rise to a two-dimensional coordination polymer [CdCl2(4,4-bipyridine)] which has been characterized by single-crystal X-ray diffraction...The reaction of L-histidine, CdCl22.5H2O and 4,4-bipyridine in methane/water gave rise to a two-dimensional coordination polymer [CdCl2(4,4-bipyridine)] which has been characterized by single-crystal X-ray diffraction. The polymer crystallizes in the orthorhombic sys- tem, space group Cmmm with a = 12.083(7), b = 11.771(7), c = 3.781(2) ? V = 537.8(6) ?, Z = 2, C10H8N2CdCl2, Mr = 339.48, Dc = 2.097 g/cm3, F(000) = 328 and (MoK? = 2.490 mm-1. The final R = 0.0658 and wR = 0.1398 for 257 observed reflections with I≥2(I).展开更多
A new complex [Cd（H2biim）2（H2O）2]·（ino）2·4H2O （H2biim = 2,2＇-biimidazole, ino = isonicotinate-N-oxide） has been prepared and characterized by single-crystal X-ray diffraction analysis, IR and fluore...A new complex [Cd（H2biim）2（H2O）2]·（ino）2·4H2O （H2biim = 2,2＇-biimidazole, ino = isonicotinate-N-oxide） has been prepared and characterized by single-crystal X-ray diffraction analysis, IR and fluorescence spectra analysis. The crystal is of triclinic system, space group P1 with a = 7.5380（6）, b = 8.0402（7）, c = 13.5094（11） , α = 104.269（1）, β = 93.604（1）, γ = 98.349（1）°, V = 780.93（11） 3, Mr = 765.00, Dc = 1.627 g/cm3, F（000） = 390, μ = 0.776 mm-1 and Z = 1. The final R = 0.0322 and wR = 0.0825 for 7038 observed reflections with I 2σ（I） and R = 0.0341 and wR = 0.0832 for all data. The title complex exhibits an infinite chain-like structure through bridging isonicotinate-N-oxide. Strong interchain hydrogen bonds between isonicotinate-N-oxide and H2biim result in the robust 3-D supramolecular architecture. Moreover, the complex shows strong photoluminescence with emission maximum at λ = 401 nm upon λex = 330 nm.展开更多
A novel coordination polymer [Eu2(C6H8O4)3(H2O)2]n?n(4,4?-bpy) (Mr = 928.51) was synthesized by the hydrothermal reaction of EuCl3?6H2O, adipic acid and 4,4?-bpy, and determined by elemental analysis, IR spectroscop...A novel coordination polymer [Eu2(C6H8O4)3(H2O)2]n?n(4,4?-bpy) (Mr = 928.51) was synthesized by the hydrothermal reaction of EuCl3?6H2O, adipic acid and 4,4?-bpy, and determined by elemental analysis, IR spectroscopy, thermal gravimetric analysis, single-crystal diffraction and fluorescence property. X-ray analysis reveals that a three-dimensional network has been formed between Eu3+ by carboxyl of adipic acid. The crystal is of orthorhombic, space group Pbcn with a = 21.870(7), b = 7.652(2), c = 19.624(6) ?, V = 3284.1(17) ?3, Z = 4, Dc = 1.878 g/cm3, μ = 3.854 mm-1, F(000) = 1824, R = 0.0345 and wR = 0.0565. The coordination polymer exhibits intensive red light under UV excitation at room temperature, which is attributed to the 5D0→7F2 transition of Eu(Ⅲ) ions.展开更多
Two lanthanide coordination polymers,{[Ln(Hbidc)(bidc)(H2O)3]-]·3 H2 O}n(H3 bidc=benzimidazole-5,6-dicarboxylic acid,Ln=Eu(1),Sm(2))have been hydrothennally synthesized.Both compounds are isostructure and crystal...Two lanthanide coordination polymers,{[Ln(Hbidc)(bidc)(H2O)3]-]·3 H2 O}n(H3 bidc=benzimidazole-5,6-dicarboxylic acid,Ln=Eu(1),Sm(2))have been hydrothennally synthesized.Both compounds are isostructure and crystallize in the P21c space group of monoclinic system.Complex1:a=11.087(6),b=8.972(5),c=23.064(13)A,β=95.027(5)°,V=2285.4(2)A3,Z=4,Mr=669.35,Dc=1.945 g/cm3,F(000)=1328,S=1.044,μ=2.827 mm-1,R=0.0393 and wR=0.0801 for 3458 observed reflections(I>2δ(I)).Complex 2:a=11.087(6),b=8.972(5),c=23.064(13)A,/3=95.027(5)°,V=2285.4(2)A3,Z=4,A/r=667.74,Dc=1.941 g/cm3,F(000)=1324,S=1.071,μ=2.652 mm-1,R=0.0329 and wR=0.0809 for 3744 observed reflections(I>2δ(I)).Complexes 1 and 2 have been determined by single-crystal X-ray diffraction analyses and further characterized by elemental analyses.IR spectroscopy,and thermogravimetric analyses(TGA).The single-crystal X-ray diffraction analysis reveals that complexes 1 and 2 are the isostructural 1D zigzag chain structures,which are further extended into a 3D supramolecular structure through hydrogen bonds and stacking interactions.Furthermore,the thermal stability,UV-vis absorption spectra and fluorescent properties of complexes 1 and 2 have been investigated and discussed in detail.展开更多
The two title complexes, [Cd{3,5-（NO2）2sal}（2,2′-bipy）]n 1 and [Mn{3,5- （NO2）2sal}（2,2′-bipy）]n 2 （3,5-（NO2）2sal = 3,5-dinitrosalicylate, 2,2＇-bipy = 2,2′-bipyridine）, were synthesized by the hydrother...The two title complexes, [Cd{3,5-（NO2）2sal}（2,2′-bipy）]n 1 and [Mn{3,5- （NO2）2sal}（2,2′-bipy）]n 2 （3,5-（NO2）2sal = 3,5-dinitrosalicylate, 2,2＇-bipy = 2,2′-bipyridine）, were synthesized by the hydrothermal reaction and structurally characterized. Complex 1 crystallizes in triclinic, space group P1, a = 5.581（4）, b = 12.071（8）, c = 12.88（1）A, α= 92.10（3）,β= 96.73（3）, γ = 102.02（2）°, C17H10N407Cd, Mr = 494.69, V= 841（1）A3, Z = 2, Dc = 1.954 g/cm3, F（000） = 488, μ= 1.353 mm^-1, R = 0.0248 and wR = 0.0761. Complex 2 crystallizes in monoclinic with space group P21/c, a = 8.604（3）, b = 23.88（1）, c = 8.894（3） A, β = 102.45（1）°, C17H10N407Mn, Mr = 437.23, V= 1785（1） A3, Z=.4, Dc = 1.627 g/cm3, F（000） = 884, μ = 0.791 mm^-1, R = 0.0471 and wR = 0.1250. Complex 1 possesses an infinite 1D polymeric chain structure consisting of the repeated basic four-membered ring units （Cd2O2） and eight-membered ring units （CdOCO）2. Compound 2displays a linear 1D chain through Mn（Ⅱ） atoms and bridging carboxylate groups of 3,5-dinitrosalicylic acid ligands with the Mn…Mn separation of 4.472（2）A. The fluorescence properties and cyclic voltammetric behaviors of the complexes are also reported.展开更多
A new Cd（II） complex [Cd（C12H6OaN2）（Phen）ffH2O）]＇3H2O with 2,2＂-bipyridine- 3,3＂-dicarboxylic acid as a ligand has been synthesized. Crystal data for the title complex are as follows： monoclinic, space grou...A new Cd（II） complex [Cd（C12H6OaN2）（Phen）ffH2O）]＇3H2O with 2,2＂-bipyridine- 3,3＂-dicarboxylic acid as a ligand has been synthesized. Crystal data for the title complex are as follows： monoclinic, space group P2dn, a = 12.8458（5）, b = 17.9131（7）, c = 15.2960（6） A, β = 111.7430（10）°, V = 3269.3（2） A3, Dc = 1.581 g/cm3, Z = 4,/a（MoKa） = 0.731 mm-1, F（000） = 1580, the R = 0.0244 and wR = 0.0605. In the title complex, the central Cd（ll） ion is located in a distorted octahedral coordination environment. The electrochemical and fluorescent properties of the title complex were studied. The results show that the electron transfer of the title complex is irreversible in the electrode reaction and it has a broad emission peak in the range of 470-508 nm with the excitation wavelength of 488 nm.展开更多
Four new coordination compounds, [Zn(dba)(bpy)]n (1), {[Zn(dba)(phen)]·2H2O}n (2), [Cd(dba)(bpy)(H2O)2] (3) and [Cd2(dba)2(phen)2]n (4) (H2dba = 2,5-dihydroxy-p-benzenediacetic acid, bpy = 2,2′-bipyridine, phen ...Four new coordination compounds, [Zn(dba)(bpy)]n (1), {[Zn(dba)(phen)]·2H2O}n (2), [Cd(dba)(bpy)(H2O)2] (3) and [Cd2(dba)2(phen)2]n (4) (H2dba = 2,5-dihydroxy-p-benzenediacetic acid, bpy = 2,2′-bipyridine, phen = 1,10-phenanthroline) have been prepared via solvothermal method and characterized by sin-gle-crystal X-ray diffraction, infrared spectroscopy, elemental analysis and powder X-ray diffraction. 1 and 2 possess 1D infinite chain structures. Complex 3 exhibits a mononuclear structure. Complex 4 owns binuclear symmetry units, which were bridged via the dba ligands forming a 2D framework. The fluorescence properties of 1―4 have been studied.展开更多
A new μ-chloro-bridged one-dimensional coordination polymer [Cd（dmbpy）Cl2]a （dmbpy = 4,4＇-dimethyl-2,2＇-bipyridine） has been synthesized and structurally characterized by elemental analyses, IR, UV spectra and ...A new μ-chloro-bridged one-dimensional coordination polymer [Cd（dmbpy）Cl2]a （dmbpy = 4,4＇-dimethyl-2,2＇-bipyridine） has been synthesized and structurally characterized by elemental analyses, IR, UV spectra and single-crystal X-ray diffraction. The complex crystallizes in the monoclinic system, space group C2/c with a = 17.745（4）, b = 10.326（2）, c = 7.3382（15）A, β = 106.85（3）°, V = 1286.9（4）A^3, Z = 4, C12H12N2Cl2Cd, Mr = 367.54, Dc = 1.897 g/cm^3, F（000） = 720, 2（MoKα） = 0.71073 A,μ= 2.089 mm^-1, R = 0.0368 and wR = 0.1048 for 1041 observed reflections （I 〉 2σ（I））. Cadmium（Ⅱ） adopts a distorted octahedral coordination geometry and adjacent coordination chains are intercalated in a zipper-like fashion into 2D layers through the π-π stacking interactions between dmbpy. Fluorescent analyses show that it exhibits intense blue photoluminescence in both DMF and DMSO solutions at room temperature.展开更多
Two mixed-ligand polymeric complexes formulated as {[Zn（pda）（bpy）]·0.5H2O}n （pda = 1,4-phenylenediacetate, bpy = 2,2＇-bipyridine） 1 and {[Cd（pda）（bpy）]·1.5H2O}n 2 have been hydrothermally synthesi...Two mixed-ligand polymeric complexes formulated as {[Zn（pda）（bpy）]·0.5H2O}n （pda = 1,4-phenylenediacetate, bpy = 2,2＇-bipyridine） 1 and {[Cd（pda）（bpy）]·1.5H2O}n 2 have been hydrothermally synthesized. Single-crystal X-ray diffraction analyses reveal that the structures of complexes 1 and 2 possess similar one-dimensional zigzag chains. Crystal data for compound 1： monoclinic, space group P21/c, a = 15.965（2）, b = 8.305（1）, c= 14.856（2） °A, β= 111.048（2）°, Mr = 422.73, V = 1838.2（4）°A^3, Z = 4, Dc = 1.528 g/cm^3, μ= 1.368 mm^-1, F（000） = 868, the final R = 0.0783 and wR = 0.1469 （w =1/[σ^2（Fo^2） ＋ （0.0351P）^2＋ 8.0014P], where P = （Fo^2 ＋ 2Fc^2）/3） based on 2025 observed reflections with I〉 2σ（I）; and those for compound 2： monoclinic, space group C2/c, a = 29.921 （7）, b = 8.5400（17）, c = 15.320（3） °A,β= 99.59（3）°, Mr = 487.75, V = 3859.9（14） °A^3, Z = 8, Dc = 1.668 g/cm^3, μ= 1.169 mm^-1, F（000） = 1936, the final R = 0.0723 and wR = 0.1612 （w = 1/[σ^2（Fo^2） ＋ （0.0681P）^2 ＋ 55.9577P], where P = （Fo^2 ＋ 2Fc^2）/3） based on 2130 observed reflections with I〉 2σ（I）. Fluorescent analyses show that both complexes exhibit intense blue luminescence （λmax = 485 nm for 1 and 475 nm for 2） upon excitation at 330 nm.展开更多
A new 2D metal coordination polymer(MCP),[Mn(pzdc)0.5(L)]n(1,pzdc=pyrazine-2,3-dicar-boxylic acid,HL=3-(2-pyridyl)pyrazole),was synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffr...A new 2D metal coordination polymer(MCP),[Mn(pzdc)0.5(L)]n(1,pzdc=pyrazine-2,3-dicar-boxylic acid,HL=3-(2-pyridyl)pyrazole),was synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction,powder XRD,FT-IR,TG,fluorescence and elemental analysis techniques.Pale yellow crystals crystallize in orthorhombic system,space group Fdd2 with a=11.2368(6),b=38.280(2),c=10.5682(6)Å,V=4545.9(4)Å3,C11H7MnN4O2,Mr=282.15,Dc=1.649 g/cm3,μ(MoKα)=1.159 mm^(-1),F(000)=2272,Z=16,the final R=0.0613 and wR=0.1773 for 2856 observed reflections(I>2σ(I)).It shows a two-dimensional network structure and is further assembled into a three-dimensional supramolecular framework via hydrogen bonds and abundantπ-πinteractions.In addition,we analyzed natural bond orbital(NBO)of 1 in using the PBE0/LANL2DZ method established in Gaussian 03 Program.There is obvious covalent interaction between the coordinated atoms and Mn(Ⅱ)ions.展开更多
The title complex, formulated as {[Cd（pda）（phen）]·3H2O}, 1 （pda = 1,4-phenylenediacetate, phen = 1,10′-phenanthroline）, has been hydrothermally synthesized and determimned by X-ray crystallography. Crystal...The title complex, formulated as {[Cd（pda）（phen）]·3H2O}, 1 （pda = 1,4-phenylenediacetate, phen = 1,10′-phenanthroline）, has been hydrothermally synthesized and determimned by X-ray crystallography. Crystallographic data： triclinic, space group P1^-, a = 10.375 （7）, b = 10.435（1）, c = 12.040（1） A.α = 68.503（1）, ,β= 86.371（1）, γ= 66.231（1）°, Mr = 538.82, V = 1104.5（8） ,A^3, Z = 2, Dc = 1.620 g/cm^3,μ = 1.035 mm^-1, F（000） = 544, the final R = 0.0380 and wR = 0.0985 （w = 1/[σ^2（F0^2） ＋ （0.0559P）^2 ＋ 1.5319P], where P = （F0^2＋ 2Fc^2）/3） based on 3444 observed reflections with I 〉2σ（I）. Complex 1 features a two-dimensional layer. Fluorescent analysis reveals that it exhibits intense green luminescence with the maximum at around 516 nm.展开更多
Two novel Cd(Ⅱ) coordination polymers, [Cd 2(C 10H 2O 8)\5(H 2O) 6] n (1) and [Cd 4(C 6H 4O 2N) 8(H 2O) 4] n (2) (C 10H 2O 8=1,2,4,5-benzenetetracarboxyl and C 6H 4O 2N=nicotinato), were hydrothermally synthesized an...Two novel Cd(Ⅱ) coordination polymers, [Cd 2(C 10H 2O 8)\5(H 2O) 6] n (1) and [Cd 4(C 6H 4O 2N) 8(H 2O) 4] n (2) (C 10H 2O 8=1,2,4,5-benzenetetracarboxyl and C 6H 4O 2N=nicotinato), were hydrothermally synthesized and characterized by X-ray diffraction of the single-crystal and fluorescence spectra. Complex 1 crystallizes in triclinic system, space group P1 with a=0.559 62(7) nm, b=0.777 58(6) nm, c=0.969 75(10) nm, α=111.981(5)°, β=101.649(6)°, γ=98.240(5)°, and Z=1. Final R=0.024 8(wR=0.078 5). Complex 2 belongs to orthorhombic system, space group Pbca with unit cell dimensions a=1.144 94(19) nm, b=1.209 69(6) nm, c=1.740 73(8) nm and Z=8. Final R=0.018 5(wR=0.034 8). Both the two complexes are coordination polymers with a two-dimensional infinite structure, the repeat unit is [Cd 2(C 10H 2O 8)(H 2O) 6] (1) and [Cd 4(C 6H 4O 2N) 8(H 2O) 4] (2) which are bridged by the ligands of 1,2,4,5-benzenetetracarboxyl(C 10H 2O 8) and nicotinato(NA), respectively. The two polymers show strong fluorescence with λ em=433 nm(λ ex=333 nm, 1) and λ em=423 nm(λ ex=330 nm, 2) in the solid state at room temperature. The emissions observed in the polymers are tentatively assigned to the ligands fluorescence(LLCT).展开更多
基金supported by the National Natural Science Foundation of China (No. 21172105)the Foundation of the Education Department of Henan Province (No. 2011A150021)
文摘A new cadmium（Ⅱ） polymer [Cd（tdc）（Phen）]n 1 （H2tdc = thiophene-3,4-dicar-boxylic acid, Phen = 1,10-phenanthroline） was synthesized under hydrothermal conditions. The compound crystallizes in the triclinic system, space group P , with a = 7.3150（10）, b = 10.3598（14）, c = 10.8784（15） , α = 82.2740（10）, β = 72.9730（10）, γ = 80.236（2）°, V = 773.68（18） 3, Z = 2, Mr = 462.74, Dc = 1.986 Mg/m3, μ = 1.58 mm-1, F（000） = 456, the final R = 0.0218 and wR = 0.0465 for 3361 observed reflections with Ⅰ 〉 2σ（Ⅰ）. The compound presents a one-dimensional （1-D） double-stranded structure and exhibits fluorescent emission at room temperature. Furthermore, infrared spectroscopy, elemental analyses, thermogravimetric analysis and powder X-ray diffraction properties of the compound are also investigated.
基金This work was supported by the National Natural Science Foundation of China (No. 20231020)
文摘The reaction of L-histidine, CdCl22.5H2O and 4,4-bipyridine in methane/water gave rise to a two-dimensional coordination polymer [CdCl2(4,4-bipyridine)] which has been characterized by single-crystal X-ray diffraction. The polymer crystallizes in the orthorhombic sys- tem, space group Cmmm with a = 12.083(7), b = 11.771(7), c = 3.781(2) ? V = 537.8(6) ?, Z = 2, C10H8N2CdCl2, Mr = 339.48, Dc = 2.097 g/cm3, F(000) = 328 and (MoK? = 2.490 mm-1. The final R = 0.0658 and wR = 0.1398 for 257 observed reflections with I≥2(I).
基金supported by the National Natural Science Foundation of China (No. 20772042)
文摘A new complex [Cd（H2biim）2（H2O）2]·（ino）2·4H2O （H2biim = 2,2＇-biimidazole, ino = isonicotinate-N-oxide） has been prepared and characterized by single-crystal X-ray diffraction analysis, IR and fluorescence spectra analysis. The crystal is of triclinic system, space group P1 with a = 7.5380（6）, b = 8.0402（7）, c = 13.5094（11） , α = 104.269（1）, β = 93.604（1）, γ = 98.349（1）°, V = 780.93（11） 3, Mr = 765.00, Dc = 1.627 g/cm3, F（000） = 390, μ = 0.776 mm-1 and Z = 1. The final R = 0.0322 and wR = 0.0825 for 7038 observed reflections with I 2σ（I） and R = 0.0341 and wR = 0.0832 for all data. The title complex exhibits an infinite chain-like structure through bridging isonicotinate-N-oxide. Strong interchain hydrogen bonds between isonicotinate-N-oxide and H2biim result in the robust 3-D supramolecular architecture. Moreover, the complex shows strong photoluminescence with emission maximum at λ = 401 nm upon λex = 330 nm.
基金The project was supported by the Natural Science Foundation of Hebei Province (No. F2004000130)
文摘A novel coordination polymer [Eu2(C6H8O4)3(H2O)2]n?n(4,4?-bpy) (Mr = 928.51) was synthesized by the hydrothermal reaction of EuCl3?6H2O, adipic acid and 4,4?-bpy, and determined by elemental analysis, IR spectroscopy, thermal gravimetric analysis, single-crystal diffraction and fluorescence property. X-ray analysis reveals that a three-dimensional network has been formed between Eu3+ by carboxyl of adipic acid. The crystal is of orthorhombic, space group Pbcn with a = 21.870(7), b = 7.652(2), c = 19.624(6) ?, V = 3284.1(17) ?3, Z = 4, Dc = 1.878 g/cm3, μ = 3.854 mm-1, F(000) = 1824, R = 0.0345 and wR = 0.0565. The coordination polymer exhibits intensive red light under UV excitation at room temperature, which is attributed to the 5D0→7F2 transition of Eu(Ⅲ) ions.
基金supported by the Key Basic Research Project of Hebei Province(18961031D)the High-Level Talents Funding Project of Hebei Province(A201400233)+2 种基金the Science and Technology Research Project of Hebei’s Colleges and University(No.BJ 2017035)the Science and Technology Research and Development Program of Hebei Province,Zhangjiakou City(17120011D)the Doctoral Foundation of Hebei North University(12995557)
文摘Two lanthanide coordination polymers,{[Ln(Hbidc)(bidc)(H2O)3]-]·3 H2 O}n(H3 bidc=benzimidazole-5,6-dicarboxylic acid,Ln=Eu(1),Sm(2))have been hydrothennally synthesized.Both compounds are isostructure and crystallize in the P21c space group of monoclinic system.Complex1:a=11.087(6),b=8.972(5),c=23.064(13)A,β=95.027(5)°,V=2285.4(2)A3,Z=4,Mr=669.35,Dc=1.945 g/cm3,F(000)=1328,S=1.044,μ=2.827 mm-1,R=0.0393 and wR=0.0801 for 3458 observed reflections(I>2δ(I)).Complex 2:a=11.087(6),b=8.972(5),c=23.064(13)A,/3=95.027(5)°,V=2285.4(2)A3,Z=4,A/r=667.74,Dc=1.941 g/cm3,F(000)=1324,S=1.071,μ=2.652 mm-1,R=0.0329 and wR=0.0809 for 3744 observed reflections(I>2δ(I)).Complexes 1 and 2 have been determined by single-crystal X-ray diffraction analyses and further characterized by elemental analyses.IR spectroscopy,and thermogravimetric analyses(TGA).The single-crystal X-ray diffraction analysis reveals that complexes 1 and 2 are the isostructural 1D zigzag chain structures,which are further extended into a 3D supramolecular structure through hydrogen bonds and stacking interactions.Furthermore,the thermal stability,UV-vis absorption spectra and fluorescent properties of complexes 1 and 2 have been investigated and discussed in detail.
基金the National Natural Science Foundation of China (No. 20431010)
文摘The two title complexes, [Cd{3,5-（NO2）2sal}（2,2′-bipy）]n 1 and [Mn{3,5- （NO2）2sal}（2,2′-bipy）]n 2 （3,5-（NO2）2sal = 3,5-dinitrosalicylate, 2,2＇-bipy = 2,2′-bipyridine）, were synthesized by the hydrothermal reaction and structurally characterized. Complex 1 crystallizes in triclinic, space group P1, a = 5.581（4）, b = 12.071（8）, c = 12.88（1）A, α= 92.10（3）,β= 96.73（3）, γ = 102.02（2）°, C17H10N407Cd, Mr = 494.69, V= 841（1）A3, Z = 2, Dc = 1.954 g/cm3, F（000） = 488, μ= 1.353 mm^-1, R = 0.0248 and wR = 0.0761. Complex 2 crystallizes in monoclinic with space group P21/c, a = 8.604（3）, b = 23.88（1）, c = 8.894（3） A, β = 102.45（1）°, C17H10N407Mn, Mr = 437.23, V= 1785（1） A3, Z=.4, Dc = 1.627 g/cm3, F（000） = 884, μ = 0.791 mm^-1, R = 0.0471 and wR = 0.1250. Complex 1 possesses an infinite 1D polymeric chain structure consisting of the repeated basic four-membered ring units （Cd2O2） and eight-membered ring units （CdOCO）2. Compound 2displays a linear 1D chain through Mn（Ⅱ） atoms and bridging carboxylate groups of 3,5-dinitrosalicylic acid ligands with the Mn…Mn separation of 4.472（2）A. The fluorescence properties and cyclic voltammetric behaviors of the complexes are also reported.
基金Fund of Science and Technology Committee of Hunan Province(No.2012GK3030)Scientific Research Fund of Hunan Provincial Education Department(No.11C0186)+1 种基金Hengyang Bureau of Science and Technology(No.2011kG28)the Key Discipline Project of Hunan Province
文摘A new Cd（II） complex [Cd（C12H6OaN2）（Phen）ffH2O）]＇3H2O with 2,2＂-bipyridine- 3,3＂-dicarboxylic acid as a ligand has been synthesized. Crystal data for the title complex are as follows： monoclinic, space group P2dn, a = 12.8458（5）, b = 17.9131（7）, c = 15.2960（6） A, β = 111.7430（10）°, V = 3269.3（2） A3, Dc = 1.581 g/cm3, Z = 4,/a（MoKa） = 0.731 mm-1, F（000） = 1580, the R = 0.0244 and wR = 0.0605. In the title complex, the central Cd（ll） ion is located in a distorted octahedral coordination environment. The electrochemical and fluorescent properties of the title complex were studied. The results show that the electron transfer of the title complex is irreversible in the electrode reaction and it has a broad emission peak in the range of 470-508 nm with the excitation wavelength of 488 nm.
基金Supported by the National Natural Science Foundation of China (Grant No. 20631030)the Natural Science Foundation of Tianjin (Grant No. 08ZCGHHZ01100)the Specialized Research Fund for the Doctoral Program of Higher Education (Grant No. 20060055039) of China
文摘Four new coordination compounds, [Zn(dba)(bpy)]n (1), {[Zn(dba)(phen)]·2H2O}n (2), [Cd(dba)(bpy)(H2O)2] (3) and [Cd2(dba)2(phen)2]n (4) (H2dba = 2,5-dihydroxy-p-benzenediacetic acid, bpy = 2,2′-bipyridine, phen = 1,10-phenanthroline) have been prepared via solvothermal method and characterized by sin-gle-crystal X-ray diffraction, infrared spectroscopy, elemental analysis and powder X-ray diffraction. 1 and 2 possess 1D infinite chain structures. Complex 3 exhibits a mononuclear structure. Complex 4 owns binuclear symmetry units, which were bridged via the dba ligands forming a 2D framework. The fluorescence properties of 1―4 have been studied.
基金the Natural Science Foundation of Education Department of Guizhou Province(No.2007060)the Science and Technology Foundation of Guizhou Province and the National Natural Science Foundation of China(No.30672515)
文摘A new μ-chloro-bridged one-dimensional coordination polymer [Cd（dmbpy）Cl2]a （dmbpy = 4,4＇-dimethyl-2,2＇-bipyridine） has been synthesized and structurally characterized by elemental analyses, IR, UV spectra and single-crystal X-ray diffraction. The complex crystallizes in the monoclinic system, space group C2/c with a = 17.745（4）, b = 10.326（2）, c = 7.3382（15）A, β = 106.85（3）°, V = 1286.9（4）A^3, Z = 4, C12H12N2Cl2Cd, Mr = 367.54, Dc = 1.897 g/cm^3, F（000） = 720, 2（MoKα） = 0.71073 A,μ= 2.089 mm^-1, R = 0.0368 and wR = 0.1048 for 1041 observed reflections （I 〉 2σ（I））. Cadmium（Ⅱ） adopts a distorted octahedral coordination geometry and adjacent coordination chains are intercalated in a zipper-like fashion into 2D layers through the π-π stacking interactions between dmbpy. Fluorescent analyses show that it exhibits intense blue photoluminescence in both DMF and DMSO solutions at room temperature.
基金This work was supported by the National Natural Science Foundation of China (No. 20231020) and Natural Science Foundation of Fujian Province
文摘Two mixed-ligand polymeric complexes formulated as {[Zn（pda）（bpy）]·0.5H2O}n （pda = 1,4-phenylenediacetate, bpy = 2,2＇-bipyridine） 1 and {[Cd（pda）（bpy）]·1.5H2O}n 2 have been hydrothermally synthesized. Single-crystal X-ray diffraction analyses reveal that the structures of complexes 1 and 2 possess similar one-dimensional zigzag chains. Crystal data for compound 1： monoclinic, space group P21/c, a = 15.965（2）, b = 8.305（1）, c= 14.856（2） °A, β= 111.048（2）°, Mr = 422.73, V = 1838.2（4）°A^3, Z = 4, Dc = 1.528 g/cm^3, μ= 1.368 mm^-1, F（000） = 868, the final R = 0.0783 and wR = 0.1469 （w =1/[σ^2（Fo^2） ＋ （0.0351P）^2＋ 8.0014P], where P = （Fo^2 ＋ 2Fc^2）/3） based on 2025 observed reflections with I〉 2σ（I）; and those for compound 2： monoclinic, space group C2/c, a = 29.921 （7）, b = 8.5400（17）, c = 15.320（3） °A,β= 99.59（3）°, Mr = 487.75, V = 3859.9（14） °A^3, Z = 8, Dc = 1.668 g/cm^3, μ= 1.169 mm^-1, F（000） = 1936, the final R = 0.0723 and wR = 0.1612 （w = 1/[σ^2（Fo^2） ＋ （0.0681P）^2 ＋ 55.9577P], where P = （Fo^2 ＋ 2Fc^2）/3） based on 2130 observed reflections with I〉 2σ（I）. Fluorescent analyses show that both complexes exhibit intense blue luminescence （λmax = 485 nm for 1 and 475 nm for 2） upon excitation at 330 nm.
基金Jilin Science and Technology Development Program(JJKH20180776KJ)Jilin Normal University Graduate Innovation Program(201939)。
文摘A new 2D metal coordination polymer(MCP),[Mn(pzdc)0.5(L)]n(1,pzdc=pyrazine-2,3-dicar-boxylic acid,HL=3-(2-pyridyl)pyrazole),was synthesized under hydrothermal conditions and characterized by single-crystal X-ray diffraction,powder XRD,FT-IR,TG,fluorescence and elemental analysis techniques.Pale yellow crystals crystallize in orthorhombic system,space group Fdd2 with a=11.2368(6),b=38.280(2),c=10.5682(6)Å,V=4545.9(4)Å3,C11H7MnN4O2,Mr=282.15,Dc=1.649 g/cm3,μ(MoKα)=1.159 mm^(-1),F(000)=2272,Z=16,the final R=0.0613 and wR=0.1773 for 2856 observed reflections(I>2σ(I)).It shows a two-dimensional network structure and is further assembled into a three-dimensional supramolecular framework via hydrogen bonds and abundantπ-πinteractions.In addition,we analyzed natural bond orbital(NBO)of 1 in using the PBE0/LANL2DZ method established in Gaussian 03 Program.There is obvious covalent interaction between the coordinated atoms and Mn(Ⅱ)ions.
基金This work was supported by the National Natural Science Foundation of China (No. 20231020) and Natural Science Foundation of Fujian Province
文摘The title complex, formulated as {[Cd（pda）（phen）]·3H2O}, 1 （pda = 1,4-phenylenediacetate, phen = 1,10′-phenanthroline）, has been hydrothermally synthesized and determimned by X-ray crystallography. Crystallographic data： triclinic, space group P1^-, a = 10.375 （7）, b = 10.435（1）, c = 12.040（1） A.α = 68.503（1）, ,β= 86.371（1）, γ= 66.231（1）°, Mr = 538.82, V = 1104.5（8） ,A^3, Z = 2, Dc = 1.620 g/cm^3,μ = 1.035 mm^-1, F（000） = 544, the final R = 0.0380 and wR = 0.0985 （w = 1/[σ^2（F0^2） ＋ （0.0559P）^2 ＋ 1.5319P], where P = （F0^2＋ 2Fc^2）/3） based on 3444 observed reflections with I 〉2σ（I）. Complex 1 features a two-dimensional layer. Fluorescent analysis reveals that it exhibits intense green luminescence with the maximum at around 516 nm.
文摘Two novel Cd(Ⅱ) coordination polymers, [Cd 2(C 10H 2O 8)\5(H 2O) 6] n (1) and [Cd 4(C 6H 4O 2N) 8(H 2O) 4] n (2) (C 10H 2O 8=1,2,4,5-benzenetetracarboxyl and C 6H 4O 2N=nicotinato), were hydrothermally synthesized and characterized by X-ray diffraction of the single-crystal and fluorescence spectra. Complex 1 crystallizes in triclinic system, space group P1 with a=0.559 62(7) nm, b=0.777 58(6) nm, c=0.969 75(10) nm, α=111.981(5)°, β=101.649(6)°, γ=98.240(5)°, and Z=1. Final R=0.024 8(wR=0.078 5). Complex 2 belongs to orthorhombic system, space group Pbca with unit cell dimensions a=1.144 94(19) nm, b=1.209 69(6) nm, c=1.740 73(8) nm and Z=8. Final R=0.018 5(wR=0.034 8). Both the two complexes are coordination polymers with a two-dimensional infinite structure, the repeat unit is [Cd 2(C 10H 2O 8)(H 2O) 6] (1) and [Cd 4(C 6H 4O 2N) 8(H 2O) 4] (2) which are bridged by the ligands of 1,2,4,5-benzenetetracarboxyl(C 10H 2O 8) and nicotinato(NA), respectively. The two polymers show strong fluorescence with λ em=433 nm(λ ex=333 nm, 1) and λ em=423 nm(λ ex=330 nm, 2) in the solid state at room temperature. The emissions observed in the polymers are tentatively assigned to the ligands fluorescence(LLCT).
