A new Cd（Ⅱ） coordination polymer, namely, [Cd（1,3-bip）（3,5-pdc）]n （1,3-bip = 1,3-bis（imidazol）propane and 3,5-pdc = pyridine-3,5-dicarboxylic acid） has been synthesized under hydrothermal conditions. Compou...A new Cd（Ⅱ） coordination polymer, namely, [Cd（1,3-bip）（3,5-pdc）]n （1,3-bip = 1,3-bis（imidazol）propane and 3,5-pdc = pyridine-3,5-dicarboxylic acid） has been synthesized under hydrothermal conditions. Compound 1 was characterized by infrared spectrum, elemental analysis, powder X-ray diffraction （PXRD） and single-crystal X-ray diffraction analysis. It crystallizes in monoclinic, space group P21/c with a = 1.40178（7）, b = 1.72502（12）, c = 1.41635（6） ran, β = 92.653（4）°, V = 3.4212（3） nm3, Z = 4, C16HIsCdNsO4, Mr = 453.73, Dc = 1.762 g/cm3, F（000） = 1808,μ = 1.310 mm1, R = 0.0899 and wR = 0.1945. In compound 1, each 3,5-pdc ligand links three Cd（lI） ions and each Cd（Ⅱ） attaches to bip ligands to form a complicated 2D double-layer structure. In addition, the thermal stability and luminescent property of 1 have been studied in the solid state at room temperature.展开更多
Three new lanthanide-organic compounds, namely, [Ln_2(OH)_2(oba)(2-pc)_2]n(Ln =Er(1), Ho(2), and Dy(3))(oba = 4,4?-oxybis(benzoate), 2-pc = 2-pyrazinecarboxylic acid) have been obtained under hydrothermal conditions. ...Three new lanthanide-organic compounds, namely, [Ln_2(OH)_2(oba)(2-pc)_2]n(Ln =Er(1), Ho(2), and Dy(3))(oba = 4,4?-oxybis(benzoate), 2-pc = 2-pyrazinecarboxylic acid) have been obtained under hydrothermal conditions. These compounds are isostructural and exhibit 2 D layered structures by incorporating [Ln_4(μ_3-OH)_4]^(8+) clusters and the mixed linkers of oba and 2-pc. It is interesting that decarboxylation occurred in the ortho position and 2,3-pyrazinedicarboxylic acid was partially transformed into 2-pc under hydrothermal conditions. Compound 3 emits a typical Dy^(3+) emission spectrum. Furthermore, the PXRD, TGA and IR spectra were also studied.展开更多
Deep-level defects and random oriented configuration in perovskite crystallization process would cause the nonradiative recombination and further affect the performance of perovskite solar cells(PSCs).Herein,two metal...Deep-level defects and random oriented configuration in perovskite crystallization process would cause the nonradiative recombination and further affect the performance of perovskite solar cells(PSCs).Herein,two metal-organic frameworks(MOFs)with tunable Lewis-base passivation sites have been constructed(Cd-Httb and Cd-Httb-BDC,Httb=5-(4-(1H-1,2,4-triazole-1-yl)benzyl)-1h-tetrazole,BDC=1,4-dicarboxybenzene)to eliminate deep-level defects and simultaneously as nanostructured heterogeneous nucleation seed to assist the growth of large-grained perovskite films.Compared with the control and Cd-Httb,Cd-Httb-BDC designed with mix-ligands strategy exhibited the enhanced inducted effect on the crystallization and nucleation of high-quality perovskite films during annealing process.Consequently,the resultant Cd-Httb-BDC-modified device achieved higher power conversion efficiency(PCE)(22.18%)than the control(20.89%)and Cd-Httb(21.56%).Meanwhile,the unencapsulated Cd-Httb-BDC-modified device still maintained 90%of initial PCE after 1500 h in ambient conditions and exhibited enhanced thermal stability(85℃ in N_(2) atmosphere).This work presented a successful example of mixligands strategy on construction of high-quality MOF-assisted perovskite films for high-efficient and stable PSCs.展开更多
A three-dimensional coordination polymer,namely {[Zn2（tzba）（dmtrz）（OH）]·3H2O}n（1,H2tzba = 4-（5H-tetrazol）benzoic acid,Hdmtrz = 3,5-dimethyl-lH,l,2,4-triazole）,was hydrothermally synthesized and characte...A three-dimensional coordination polymer,namely {[Zn2（tzba）（dmtrz）（OH）]·3H2O}n（1,H2tzba = 4-（5H-tetrazol）benzoic acid,Hdmtrz = 3,5-dimethyl-lH,l,2,4-triazole）,was hydrothermally synthesized and characterized by single-crystal X-ray diffraction.It crystallizes in monoclinic system,P21/c space group with a = 8.018（11）,b = 21.04（3）,c = 11.069（14） A,β=91.26（3）°,V= 1867（4） A^3,Z = 4,Dc = 1.729 g/cm^3,F（000） = 984,μ= 2.614 mm^（-1）,R（F^2 〉 2σ（F^2）） =0.0612 and wR（F^2） = 0.1533.Topological analysis reveals that compound 1 is a（3,5）-connected structure with a Schlafli symbol of（4~2.6）（4~2.6~5.8~3）,which is a rarely observed lhh topology.In addition,the CO2 adsorption performance and luminescent property of 1 have also been studied.展开更多
A novel zero-dimensional heteronuclear cluster based on N-（phosphonomethyl）imi- no-diacetic acid （H4PMIDA） and Phen （1,10-phenanthroline）, [Zn6Co9（PMIDA）6（Phen）6（NO3）4（H2O）6]·2NO3·16H2O, has be...A novel zero-dimensional heteronuclear cluster based on N-（phosphonomethyl）imi- no-diacetic acid （H4PMIDA） and Phen （1,10-phenanthroline）, [Zn6Co9（PMIDA）6（Phen）6（NO3）4（H2O）6]·2NO3·16H2O, has been synthesized under hydrothermal conditions and characterized by elemental analysis, IR spectrum, thermal analysis, and single-crystal X-ray diffraction. The isolated 15- nuclearity cluster [Zn6Co9（PMIDA）6（Phen）6（NO3）4（H2O）6]^2＋ was constructed by four kinds of ligands, and its charges are balanced by NO3^–. Each isolated cluster is further extended into a 3D supramolecular network through π？？？π interaction and C–H…O hydrogen bonds. Moreover, the solid-state fluorescent property of this complex has also been investigated at room temperature.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 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
Under hydrothermal conditions,a new lanthanide coordination polymer,[Er3(oba)4(na)]n(1,oba=4,4?-oxybis(benzoate),na=nicotinic acid)has been synthesized.Compound 1 shows a 3D framework by incorporating tri-nuclear[Er3(...Under hydrothermal conditions,a new lanthanide coordination polymer,[Er3(oba)4(na)]n(1,oba=4,4?-oxybis(benzoate),na=nicotinic acid)has been synthesized.Compound 1 shows a 3D framework by incorporating tri-nuclear[Er3(COO)6]unit and the mixed ligands of oba2-and na-.It is interesting that decarboxylation occurred in the ortho position and 2,3-pyridinedicarboxylic acid was partially transformed into na under hydrothermal conditions.Compound 1 can be reduced into a(3,11)-connected net and displays weak second-harmonic generation response.Furthermore,the PXRD,TGA and IR spectra were also studied.展开更多
The title complex [Fe（CDTA）（H2O）]·[Fe（1,10-phen）3]·10H2O·2OH （CDTA = transcyclohexane-1,2-diamine-N,N,N,N′-tetraacetate） has been prepared and characterized by single-crystal X-ray diffraction ...The title complex [Fe（CDTA）（H2O）]·[Fe（1,10-phen）3]·10H2O·2OH （CDTA = transcyclohexane-1,2-diamine-N,N,N,N′-tetraacetate） has been prepared and characterized by single-crystal X-ray diffraction analysis. The crystal adopts space group P with a = 12.793（4）, b = 14.104（5）, c = 17.880（5）, V = 2792.2（1）3, Dc = 1.459 g/cm3, C50H66Fe2N8O21, Mr = 1226.81, F（000） = 1284, μ = 0.604 mm-1, Z = 2, R = 0.1055 and wR = 0.2581 for 8675 observed reflections （I 〉 2σ（I））. X-ray crystallography analysis exhibits that the title compound consists of two crystallographically independent molecules [Fe（CDTA）（H2O）] and [Fe（1,10-phen）3], and they are connected through O-H···O hydrogen bonds and π···π stacking interactions forming a 3D supramolecular structure. Interestingly, there is a cyclic water hexamer with chair conformation in this complex.展开更多
A novel coordination polymer, [ Ni （mal） （1,10＇-phen） （ H2O） ] n （ 1 ） （ mal = malate, 1,10＇-phen = 1,10- phenanthroline） was synthesized using malic acid which was generated from maleic acid via hydrother...A novel coordination polymer, [ Ni （mal） （1,10＇-phen） （ H2O） ] n （ 1 ） （ mal = malate, 1,10＇-phen = 1,10- phenanthroline） was synthesized using malic acid which was generated from maleic acid via hydrothermal reaction. Complex 1, which displays a two-dimensional supramolecular network, was formed by the addition reaction of Ni and maleic acid with water molecules. To our knowledge, several coordination polymers have been directly synthesized from malic acid, but these types of complexes have seldom been synthesized from maleic acid via hydrothermal reactions. When Ni（ Ⅱ ） ion was changed to Zn（ Ⅱ） ion under the same condition, two-dimensional covalent complex 2 [ Zn2 （fma） 2 （1,10＇-phen） 2 ] n （fma = fumatic acid） was formed. Furthermore, complex 2 exhibits intense photolumi- nescent property at room temperature.展开更多
A new dimeric lanthanum (Ⅲ) complex [La_2(phen)_2(C_7H_3N_2O_6)_6] (phen=1, 10-phenanthroline) was synthesized by the hydrothermal method and determined by single crystal X-ray diffraction analysis. The La(Ⅲ) ion is...A new dimeric lanthanum (Ⅲ) complex [La_2(phen)_2(C_7H_3N_2O_6)_6] (phen=1, 10-phenanthroline) was synthesized by the hydrothermal method and determined by single crystal X-ray diffraction analysis. The La(Ⅲ) ion is coordinated to seven oxygen atoms from five carboxylate groups and two nitrogen atoms from a phen ligand, forming a monocapped square antiprismatic geometry. Six carboxylate groups coordinate to two La(Ⅲ) ions in three modes which are chelating bidentate, bridging bidentate and bridging tridentate. The crystal is triclinic with space group P-1, a=1.2030(4) nm, b=1.2962(5) nm, c=1.3330(5) nm, α=104.410(5)°, β=114.048(4)°, γ=100.054 (4)°, V=1.7467 (10) nm^3, M_r=952.46, Z=2, D_c=1.811 g·cm^(-3), F(000)=944, S=1.017, μ=1.320 mm^(-1), with R1=0.0298 and wR2=0.0625.展开更多
A new quaternary mixed anion complex of gadolinium(Ⅲ), [Gd(CH 3CH 2COO) 2(N O 3)(phen)] 2, was synthesized and structurally characterized. The ESR spectr um of the complex with effective g values of 5.314, 2 47...A new quaternary mixed anion complex of gadolinium(Ⅲ), [Gd(CH 3CH 2COO) 2(N O 3)(phen)] 2, was synthesized and structurally characterized. The ESR spectr um of the complex with effective g values of 5.314, 2 473 and 1.880 in poly crys talline powder at room temperature is quite different from the U spectrum. The c oordination number of Gd 3+ is nine with a monocapped square antiprism geom etry. And the stacking effect was observed in the complex. The crystal of the co mplex belongs to triclinic with space group P 1, a=0.9626(4) n m, b=0.9732(4) nm, c=1.1758(5) nm, α=102.45(1)°, β=108.16(1) °, γ=96.68(2)°, V=1.0018(7) nm3, Z=2, D c=1.80 g·cm -3 , μ(MoKα)=33.63 mm -1, F(000)=530, GOF=1.80, R=0.023 and R w=0.027.展开更多
基金Supported by the National Natural Science Foundation of China(No.21373132)the Science Foundation of Education Department of Shaanxi Provincial Government(No.12JK0637)
文摘A new Cd（Ⅱ） coordination polymer, namely, [Cd（1,3-bip）（3,5-pdc）]n （1,3-bip = 1,3-bis（imidazol）propane and 3,5-pdc = pyridine-3,5-dicarboxylic acid） has been synthesized under hydrothermal conditions. Compound 1 was characterized by infrared spectrum, elemental analysis, powder X-ray diffraction （PXRD） and single-crystal X-ray diffraction analysis. It crystallizes in monoclinic, space group P21/c with a = 1.40178（7）, b = 1.72502（12）, c = 1.41635（6） ran, β = 92.653（4）°, V = 3.4212（3） nm3, Z = 4, C16HIsCdNsO4, Mr = 453.73, Dc = 1.762 g/cm3, F（000） = 1808,μ = 1.310 mm1, R = 0.0899 and wR = 0.1945. In compound 1, each 3,5-pdc ligand links three Cd（lI） ions and each Cd（Ⅱ） attaches to bip ligands to form a complicated 2D double-layer structure. In addition, the thermal stability and luminescent property of 1 have been studied in the solid state at room temperature.
文摘Three new lanthanide-organic compounds, namely, [Ln_2(OH)_2(oba)(2-pc)_2]n(Ln =Er(1), Ho(2), and Dy(3))(oba = 4,4?-oxybis(benzoate), 2-pc = 2-pyrazinecarboxylic acid) have been obtained under hydrothermal conditions. These compounds are isostructural and exhibit 2 D layered structures by incorporating [Ln_4(μ_3-OH)_4]^(8+) clusters and the mixed linkers of oba and 2-pc. It is interesting that decarboxylation occurred in the ortho position and 2,3-pyrazinedicarboxylic acid was partially transformed into 2-pc under hydrothermal conditions. Compound 3 emits a typical Dy^(3+) emission spectrum. Furthermore, the PXRD, TGA and IR spectra were also studied.
基金supported by the National Natural Science Foundation of China(22072034,22001050,and 21873025)the China Postdoctoral Science Foundation(2020T130147,2020M681084,and 2022M710949)+1 种基金the Postdoctoral Foundation of Heilongjiang Province(LBH-Z19059)the Natural Science Foundation of Heilongjiang Youth Fund(YQ2021B002).
文摘Deep-level defects and random oriented configuration in perovskite crystallization process would cause the nonradiative recombination and further affect the performance of perovskite solar cells(PSCs).Herein,two metal-organic frameworks(MOFs)with tunable Lewis-base passivation sites have been constructed(Cd-Httb and Cd-Httb-BDC,Httb=5-(4-(1H-1,2,4-triazole-1-yl)benzyl)-1h-tetrazole,BDC=1,4-dicarboxybenzene)to eliminate deep-level defects and simultaneously as nanostructured heterogeneous nucleation seed to assist the growth of large-grained perovskite films.Compared with the control and Cd-Httb,Cd-Httb-BDC designed with mix-ligands strategy exhibited the enhanced inducted effect on the crystallization and nucleation of high-quality perovskite films during annealing process.Consequently,the resultant Cd-Httb-BDC-modified device achieved higher power conversion efficiency(PCE)(22.18%)than the control(20.89%)and Cd-Httb(21.56%).Meanwhile,the unencapsulated Cd-Httb-BDC-modified device still maintained 90%of initial PCE after 1500 h in ambient conditions and exhibited enhanced thermal stability(85℃ in N_(2) atmosphere).This work presented a successful example of mixligands strategy on construction of high-quality MOF-assisted perovskite films for high-efficient and stable PSCs.
文摘A three-dimensional coordination polymer,namely {[Zn2（tzba）（dmtrz）（OH）]·3H2O}n（1,H2tzba = 4-（5H-tetrazol）benzoic acid,Hdmtrz = 3,5-dimethyl-lH,l,2,4-triazole）,was hydrothermally synthesized and characterized by single-crystal X-ray diffraction.It crystallizes in monoclinic system,P21/c space group with a = 8.018（11）,b = 21.04（3）,c = 11.069（14） A,β=91.26（3）°,V= 1867（4） A^3,Z = 4,Dc = 1.729 g/cm^3,F（000） = 984,μ= 2.614 mm^（-1）,R（F^2 〉 2σ（F^2）） =0.0612 and wR（F^2） = 0.1533.Topological analysis reveals that compound 1 is a（3,5）-connected structure with a Schlafli symbol of（4~2.6）（4~2.6~5.8~3）,which is a rarely observed lhh topology.In addition,the CO2 adsorption performance and luminescent property of 1 have also been studied.
基金Supported by the Youth Fund Project of Shaanxi University of Chinese Medicine(No.2015Qn22)the National Youth Natural Science Foundation of China(No.21603133)the Science Foundation of Shaanxi University of Technology(No.SLGKY15-36)
文摘A novel zero-dimensional heteronuclear cluster based on N-（phosphonomethyl）imi- no-diacetic acid （H4PMIDA） and Phen （1,10-phenanthroline）, [Zn6Co9（PMIDA）6（Phen）6（NO3）4（H2O）6]·2NO3·16H2O, has been synthesized under hydrothermal conditions and characterized by elemental analysis, IR spectrum, thermal analysis, and single-crystal X-ray diffraction. The isolated 15- nuclearity cluster [Zn6Co9（PMIDA）6（Phen）6（NO3）4（H2O）6]^2＋ was constructed by four kinds of ligands, and its charges are balanced by NO3^–. Each isolated cluster is further extended into a 3D supramolecular network through π？？？π interaction and C–H…O hydrogen bonds. Moreover, the solid-state fluorescent property of this complex has also been investigated at room temperature.
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.
文摘Under hydrothermal conditions,a new lanthanide coordination polymer,[Er3(oba)4(na)]n(1,oba=4,4?-oxybis(benzoate),na=nicotinic acid)has been synthesized.Compound 1 shows a 3D framework by incorporating tri-nuclear[Er3(COO)6]unit and the mixed ligands of oba2-and na-.It is interesting that decarboxylation occurred in the ortho position and 2,3-pyridinedicarboxylic acid was partially transformed into na under hydrothermal conditions.Compound 1 can be reduced into a(3,11)-connected net and displays weak second-harmonic generation response.Furthermore,the PXRD,TGA and IR spectra were also studied.
基金supported by Knowledge Innovation Program (No. KJCX2-EW-H01)the Chinese Academy of Sciences and National Natural Science Foundation of China (No. 21073190)
文摘The title complex [Fe（CDTA）（H2O）]·[Fe（1,10-phen）3]·10H2O·2OH （CDTA = transcyclohexane-1,2-diamine-N,N,N,N′-tetraacetate） has been prepared and characterized by single-crystal X-ray diffraction analysis. The crystal adopts space group P with a = 12.793（4）, b = 14.104（5）, c = 17.880（5）, V = 2792.2（1）3, Dc = 1.459 g/cm3, C50H66Fe2N8O21, Mr = 1226.81, F（000） = 1284, μ = 0.604 mm-1, Z = 2, R = 0.1055 and wR = 0.2581 for 8675 observed reflections （I 〉 2σ（I））. X-ray crystallography analysis exhibits that the title compound consists of two crystallographically independent molecules [Fe（CDTA）（H2O）] and [Fe（1,10-phen）3], and they are connected through O-H···O hydrogen bonds and π···π stacking interactions forming a 3D supramolecular structure. Interestingly, there is a cyclic water hexamer with chair conformation in this complex.
基金Supported by the National Natural Science Foundation of China(No20371011)
文摘A novel coordination polymer, [ Ni （mal） （1,10＇-phen） （ H2O） ] n （ 1 ） （ mal = malate, 1,10＇-phen = 1,10- phenanthroline） was synthesized using malic acid which was generated from maleic acid via hydrothermal reaction. Complex 1, which displays a two-dimensional supramolecular network, was formed by the addition reaction of Ni and maleic acid with water molecules. To our knowledge, several coordination polymers have been directly synthesized from malic acid, but these types of complexes have seldom been synthesized from maleic acid via hydrothermal reactions. When Ni（ Ⅱ ） ion was changed to Zn（ Ⅱ） ion under the same condition, two-dimensional covalent complex 2 [ Zn2 （fma） 2 （1,10＇-phen） 2 ] n （fma = fumatic acid） was formed. Furthermore, complex 2 exhibits intense photolumi- nescent property at room temperature.
文摘A new dimeric lanthanum (Ⅲ) complex [La_2(phen)_2(C_7H_3N_2O_6)_6] (phen=1, 10-phenanthroline) was synthesized by the hydrothermal method and determined by single crystal X-ray diffraction analysis. The La(Ⅲ) ion is coordinated to seven oxygen atoms from five carboxylate groups and two nitrogen atoms from a phen ligand, forming a monocapped square antiprismatic geometry. Six carboxylate groups coordinate to two La(Ⅲ) ions in three modes which are chelating bidentate, bridging bidentate and bridging tridentate. The crystal is triclinic with space group P-1, a=1.2030(4) nm, b=1.2962(5) nm, c=1.3330(5) nm, α=104.410(5)°, β=114.048(4)°, γ=100.054 (4)°, V=1.7467 (10) nm^3, M_r=952.46, Z=2, D_c=1.811 g·cm^(-3), F(000)=944, S=1.017, μ=1.320 mm^(-1), with R1=0.0298 and wR2=0.0625.
文摘A new quaternary mixed anion complex of gadolinium(Ⅲ), [Gd(CH 3CH 2COO) 2(N O 3)(phen)] 2, was synthesized and structurally characterized. The ESR spectr um of the complex with effective g values of 5.314, 2 473 and 1.880 in poly crys talline powder at room temperature is quite different from the U spectrum. The c oordination number of Gd 3+ is nine with a monocapped square antiprism geom etry. And the stacking effect was observed in the complex. The crystal of the co mplex belongs to triclinic with space group P 1, a=0.9626(4) n m, b=0.9732(4) nm, c=1.1758(5) nm, α=102.45(1)°, β=108.16(1) °, γ=96.68(2)°, V=1.0018(7) nm3, Z=2, D c=1.80 g·cm -3 , μ(MoKα)=33.63 mm -1, F(000)=530, GOF=1.80, R=0.023 and R w=0.027.
