A new Cd(II) coordination polymer, namely, [Cd3(1,2,3-BTC)2(L)2]·2.25H2O (1, L = 2-(2-chloro-6-fluorophenyl)-1H-imidazo[4,5-A][1,10]phenanthroline and 1,2,3-BTC = 1,2,3-ben- zenetricarboxylate), has bee...A new Cd(II) coordination polymer, namely, [Cd3(1,2,3-BTC)2(L)2]·2.25H2O (1, L = 2-(2-chloro-6-fluorophenyl)-1H-imidazo[4,5-A][1,10]phenanthroline and 1,2,3-BTC = 1,2,3-ben- zenetricarboxylate), has been synthesized under hydrothermal conditions. The compound was characterized by single-crystal X-ray diffraction. It crystallizes in triclinic, space group Pī with α = 11.650(2), b = 12.240(2), c = 19.760(4) A, α = 72.01(3), β = 77.11(3), γ = 83.48(3)°, V = 2609.4(9) A3, Z = 2, C56H31Cd3Cl2F2N8O14.25, Mr = 1489.99, Dc = 1.896 g/cm3, F(000) = 1466, μ(MoKa) = 1.401 mm^-1, R = 0.0401 and wR = 0.1104. Compound 1 shows a 1D chain structure, and the neigh- boring 1D chains of 1 are joined together by π···π interactions to result in a 2D supramolecular layer. In addition, the luminescent property of 1 has been studied in the solid state at room temperature.展开更多
A new ID coordination polymer, [Cda(L1)2(L2)2].H2O (1, H2L1 = 4-(carboxy- methoxy)benzoic acid and L2 = 2-(4-fluorophenyl)-I H-imidazo[4,5-f][1,10]phenanthroline), has been hydrothermally synthesized and cha...A new ID coordination polymer, [Cda(L1)2(L2)2].H2O (1, H2L1 = 4-(carboxy- methoxy)benzoic acid and L2 = 2-(4-fluorophenyl)-I H-imidazo[4,5-f][1,10]phenanthroline), has been hydrothermally synthesized and characterized by elemental analysis and single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 9.985(5), b = 10.768(5), c = 12.512(5) A, a = 68.959(5), β = 80.354(5), γ = 79.663(5)°, V= 1227.4(10) A3, Z = 1, C56H36Cd2F2N8O11, Mr = 1259.73, Dc = 1.704 g/cm3, F(000) = 630, μ(MoKa) = 0.949 mm-1, R = 0.0261 and wR = 0.0655. The L1 anions link the neighboring Cd(II) atoms to form a 1D double chain structure. The L2 ligands are alternately located on both sides of the double chains. More interestingly, the lateral L2 ligands from adjacent double chains are paired to furnish strong π-π interactions, yielding a 2D supramolecular layer. N-H...O, O-H...N and O-H...O hydrogen bonds further stabilize the structure of 1. The luminescent property of 1 was studied in solid state at room temperature.展开更多
In this work, a new Cd(Ⅱ) dimeric compound, [Cd(Cl)2(L)(H2O)]2 (1, L = 2-(4- fluorophenyl)-lH-imidazo[4,5-f][1,10]phenanthroline), has been achieved under hydrothermal conditions. The structure of compoun...In this work, a new Cd(Ⅱ) dimeric compound, [Cd(Cl)2(L)(H2O)]2 (1, L = 2-(4- fluorophenyl)-lH-imidazo[4,5-f][1,10]phenanthroline), has been achieved under hydrothermal conditions. The structure of compound 1 was determined by single-crystal X-ray diffraction. Compound 1 crystallizes in monoclinic, space group P21/c with a = 8.944(2), b = 18.781(5), c = 10.904(3) A, β = 91.392(4)°, V = 1831.2(8) A^3, Z = 2, C3sH26Cd2F2C14Cl4N8O2, Mr = 1031.27, Dc = 1.870 g/cm3, F(000) = 1016, μ(MoKα) = 1.513 mm^-1, R = 0.0532 and wR = 0.1407. Each Cd(ll) atom is in an octahedral coordination sphere, completed by two nitrogen atoms from one L ligand, two chlorine anions, and one water oxygen atom. Two chlorine anions bridge two Cd(Ⅱ) atoms to give a dimer [Cd(Cl)2(L)(H2O)]2. Adjacent dimers are stacked by one type of π…π interactions among L ligands to generate a 1D supramolecular chain. Further, the 1D supramolecular chains are stacked by another type of π…π interactions among L ligands to give a 2D supramolecular layer. Finally, the luminescent property of 1 has been studied in solid state at room temperature.展开更多
A novel Fe(II) coordination polymer [Fe(L)(trans-1,4-chdc)];~ has been hydrother- mally synthesized by using 1,4-cyclohexanedicarboxylic acid (1,4-H2chdc) and 2-(2-fluoro- phenyl)-lH-imidazo[4,5-f][1,10]phen...A novel Fe(II) coordination polymer [Fe(L)(trans-1,4-chdc)];~ has been hydrother- mally synthesized by using 1,4-cyclohexanedicarboxylic acid (1,4-H2chdc) and 2-(2-fluoro- phenyl)-lH-imidazo[4,5-f][1,10]phenanthroline (L). Crystallographic data: monoclinic, space group C2/c with a = 14.571(5), b = 32.389(6), c = 10.948(5)A, 18 = 115.186(5)°, V= 4676(3)A3, Z = 8, C27H21FFeN404, Mr = 540.33, De --- 1.535 g/cm3, F(000) = 2224, μ(MoKa) = 0.697 mmI, R = 0.0462 and wR = 0.1110. The two kinds of trans-l,4-chdc ligands link neighboring Fe(II) atoms to yield a two-dimensional layer structure. The π-π interactions between the L ligands of neighboring layers result in a three-dimensional supramolecular architecture. The IR and UV-vis spectra of the compound have been investigated in detail.展开更多
A new 1D coordination polymer, [Pb(L)(cis-1,4-chdc)]·0.5H2O (cis-1,4-chdc = 1,4-cyclohexanedicarboxylate and L = 2-(4-fluorophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline), has been synthesized under hydro...A new 1D coordination polymer, [Pb(L)(cis-1,4-chdc)]·0.5H2O (cis-1,4-chdc = 1,4-cyclohexanedicarboxylate and L = 2-(4-fluorophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline), has been synthesized under hydrothermal conditions and characterized by elemental analysis, TG and single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 9.153(5), b = 10.338(5), c = 13.074(5), α = 80.956(5), β = 89.725(5), γ = 80.534(5)°, V = 1204.8(10)3 , Z = 1, C54H44F2N8O9Pb2 , Mr = 1401.35, Dc = 1.931 g/cm3 , F(000) = 678, μ(MoKa) = 7.055 mm-1 , R = 0.0277 and wR = 0.0559. Each cis-1,4-chdc anion coordinates with two Pb(Ⅱ) atoms in a bis-chelating coordination mode. In this way, cis-1,4-chdc anions bridged the neighboring Pb(Ⅱ) atoms to generate a 1D chain structure. The L ligands from neighboring chains are paired through the strong π-π interactions to generate a fascinating 2D supramolecular layer.展开更多
A new one-dimensional Ni(Ⅱ) coordination polymer [Ni(L)(cis-1,4- chdc)]n·1.25nH2O has been synthesized under hydrothermal conditions by using 1,4-cyclohexanedicarboxylic acid (1,4-H2chdc) and 2-(3-fluor...A new one-dimensional Ni(Ⅱ) coordination polymer [Ni(L)(cis-1,4- chdc)]n·1.25nH2O has been synthesized under hydrothermal conditions by using 1,4-cyclohexanedicarboxylic acid (1,4-H2chdc) and 2-(3-fluorophenyl)- 1H-imidazo [4,5-f] [ 1,10]phenanthroline (L). Crystallographic data for the compound: triclinic, space group Pi with a = 8.777(2), b = 10.662(2), c = 13.799(3) A, a = 89.480(4), β = 73,933(3), γ = 81.980(4)°, V = 1228.2(5) A3, Z = 2, C27H22.50FN4NiO5.25, Mr = 568.70, Dc = 1.527 g/cm3, F(000) = 583,μ(MoKα) = 0.846 mm-1, R = 0.0634 and wR = 0.1465. Neighboring Ni(Ⅱ) atoms are linked by the cis-1,4-chdc ligands to generate a one-dimensional chain structure. The π-π interactions between the L ligands of neighboring chains led to the formation of a two-dimensional supramolecular layer. The elemental analysis, IR spectrum and TG of the compound have been studied.展开更多
The title coordination polymer, [Pb(L)(1,4-ndc)] 1 (L = 2-(4-fluorophenyl)-1Himidazo[4,5f1,10]phenanthroline, 1,4-ndc = naphthalene-1,4-dicarboxylic acid), has been obtained by using hydrothermal synthesis and...The title coordination polymer, [Pb(L)(1,4-ndc)] 1 (L = 2-(4-fluorophenyl)-1Himidazo[4,5f1,10]phenanthroline, 1,4-ndc = naphthalene-1,4-dicarboxylic acid), has been obtained by using hydrothermal synthesis and characterized by elemental analysis, IR and singlecrystal X-ray diffraction. It crystallizes in monoclinic, space group P21/c with a = 10.1043(11), b = 14.3162(15), c = 17.6061(18), β = 95.3990(10)°, V = 2535.5(5)3, Z = 4, C31H17FN4O4Pb, Mr = 735.68, Dc = 1.927 g/cm3, F(000) = 1416, μ(MoKa) = 6.709 mm-1, R = 0.0201 and wR = 0.0489. The 1,4-ndc dianions link neighboring Pb(II) atoms in a bis-chelating mode, yielding a one-dimensional chain structure along the c axis. The C-H···π interactions between the carbon atom of L ligand and the benzene ring of 1,4-ndc lead the one-dimensional chains to form a two-dimensional supramolecular layer. The π-π interactions between L ligand and 1,4-ndc ligand make the two-dimensional layers generate a three-dimensional supramolecular architecture. Additionally, the N-H···O hydrogen bonds further stabilize the structure of 1.展开更多
A new ligand,2-(2-methoxynaphthyl)-1H-imidazo[4,5-f][1,10]phenanthroline(mnipH),was synthesized by the condensation of 2-methoxy-1-naphthaldehyde and 5,6-diamino-1,10-phenanthroline.Then three ionic copper(I)complexes...A new ligand,2-(2-methoxynaphthyl)-1H-imidazo[4,5-f][1,10]phenanthroline(mnipH),was synthesized by the condensation of 2-methoxy-1-naphthaldehyde and 5,6-diamino-1,10-phenanthroline.Then three ionic copper(I)complexes were obtained through the reactions of[Cu(MeCN)4]ClO4,mnipH and the chelating diphosphine ligands with a molar ratio of 1:1:1.The photoluminescence and the corresponding luminescent mechanism of all copper(I)complexes in the solid state were investigated at room temperature.展开更多
A new Pb(Ⅱ) coordination polymer [Pb(L1)(L2)]·1.25H2O has been synthesized with 2-(4-fluorophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline (L1) and sebacic acid (H2L2) under hydrothermal conditions. Cr...A new Pb(Ⅱ) coordination polymer [Pb(L1)(L2)]·1.25H2O has been synthesized with 2-(4-fluorophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline (L1) and sebacic acid (H2L2) under hydrothermal conditions. Crystallographic data: triclinic, space group Pī with a=8.4890(17), b=12.471(3), c=14.604(3), α=67.04(3), β=74.08(3), γ=85.80(3)°, V=1368.0(5)3 , Z=1, C58H59F2N8O10.5Pb2 , Mr=1488.51, Dc=1.807g/cm3 , F(000)=729, μ(MoKa)=6.221mm-1 , R=0.0283 and wR=0.0564. The L2 dianions bridge neighboring Pb(Ⅱ) atoms to form a two-dimensional layer structure. The π-π interactions between the L1 ligands of neighboring layers led to a three-dimensional supramolecular architecture. The IR and TGA of the complex have been studied in detail.展开更多
Complex [Zn(L)(SO4)]0.5H20 (L = 2-(2-chloro-6-fluorophenyl)-lH-imidazo[4,5- J][1,10]phenanthroline) has been synthesized under hydrothermal conditions. The compound was characterized by elemental analysis, IR,...Complex [Zn(L)(SO4)]0.5H20 (L = 2-(2-chloro-6-fluorophenyl)-lH-imidazo[4,5- J][1,10]phenanthroline) has been synthesized under hydrothermal conditions. The compound was characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction. It crystallizes in monoclinic, space group P21/n with a = 9.9916(7), b = 12.3834(9), c = 29.259(2) A, fl = 97.7720(10)°, V = 3587.0(4) A^3, Z = 2, C76H41CI4F4NI60952Zn2, Mr = 1734.91, Dc = 1.606 g/cm^3, F(000) = 1754, p(MoKa) = 0.959 mm-1, R = 0.0492 and wR = 0.1385. The asymmetric unit of 1 contains one Zn(lI) atom, two L ligands, one sulfate anion and half a water molecule. Each Zn(lI) atom is five-coordinated by four nitrogen atoms from two different L ligands and one sulfate oxygen atom in a tetragonal pyramidal coordination environment. The N-H'"O hydrogen bonds link the discrete structure of 1 into a 2D supramolecular architecture. The photoluminescent property of 1 has also been studied in the solid state at room temperature.展开更多
The title complex,[Zn(ip)2(H2O)2][ZnCl4]·H2O·2DMF 1(ip=imidazo[4,5-f][1,10] phenanthroline),has been synthesized via the slow evaporation of concentrated reaction solution at room temperature.It was ch...The title complex,[Zn(ip)2(H2O)2][ZnCl4]·H2O·2DMF 1(ip=imidazo[4,5-f][1,10] phenanthroline),has been synthesized via the slow evaporation of concentrated reaction solution at room temperature.It was characterized by single-crystal X-ray diffraction.Crystal data for C32H36Cl4N10O5Zn2:white prism,0.17mm×0.15mm×0.10mm,monoclinic,space group P2/c,a=11.928(8),b=9.868(6),c=16.520(11),β=104.879(12)°,V=1879(2)3,Z=2,Mr=913.25,Dc=1.614 g/cm3,F(000)=932,μ=1.616 mm-1,λ(MoKα)=0.71073,GOOF=1.045,R=0.0710 and wR=0.1755 for 3055 observed reflections with I 〉 2σ(I). X-ray diffraction study reveals that the title complex has an interesting 3D architecture via hydrogen bonding interactions and π-π interactions. The IR, TGA, XRD and luminescent properties of complex 1 were also studied.展开更多
基金Supported by the Science and Technology Research Projects of the Education Committee of Jilin Province(No.2013212)
文摘A new Cd(II) coordination polymer, namely, [Cd3(1,2,3-BTC)2(L)2]·2.25H2O (1, L = 2-(2-chloro-6-fluorophenyl)-1H-imidazo[4,5-A][1,10]phenanthroline and 1,2,3-BTC = 1,2,3-ben- zenetricarboxylate), has been synthesized under hydrothermal conditions. The compound was characterized by single-crystal X-ray diffraction. It crystallizes in triclinic, space group Pī with α = 11.650(2), b = 12.240(2), c = 19.760(4) A, α = 72.01(3), β = 77.11(3), γ = 83.48(3)°, V = 2609.4(9) A3, Z = 2, C56H31Cd3Cl2F2N8O14.25, Mr = 1489.99, Dc = 1.896 g/cm3, F(000) = 1466, μ(MoKa) = 1.401 mm^-1, R = 0.0401 and wR = 0.1104. Compound 1 shows a 1D chain structure, and the neigh- boring 1D chains of 1 are joined together by π···π interactions to result in a 2D supramolecular layer. In addition, the luminescent property of 1 has been studied in the solid state at room temperature.
基金Supported by Jilin Province Science and Technology Development projects (No. 201105085)
文摘A new ID coordination polymer, [Cda(L1)2(L2)2].H2O (1, H2L1 = 4-(carboxy- methoxy)benzoic acid and L2 = 2-(4-fluorophenyl)-I H-imidazo[4,5-f][1,10]phenanthroline), has been hydrothermally synthesized and characterized by elemental analysis and single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 9.985(5), b = 10.768(5), c = 12.512(5) A, a = 68.959(5), β = 80.354(5), γ = 79.663(5)°, V= 1227.4(10) A3, Z = 1, C56H36Cd2F2N8O11, Mr = 1259.73, Dc = 1.704 g/cm3, F(000) = 630, μ(MoKa) = 0.949 mm-1, R = 0.0261 and wR = 0.0655. The L1 anions link the neighboring Cd(II) atoms to form a 1D double chain structure. The L2 ligands are alternately located on both sides of the double chains. More interestingly, the lateral L2 ligands from adjacent double chains are paired to furnish strong π-π interactions, yielding a 2D supramolecular layer. N-H...O, O-H...N and O-H...O hydrogen bonds further stabilize the structure of 1. The luminescent property of 1 was studied in solid state at room temperature.
基金Supported by the Science and Technology Research Projects of the Education Committee of Jilin Province(No.2013206)
文摘In this work, a new Cd(Ⅱ) dimeric compound, [Cd(Cl)2(L)(H2O)]2 (1, L = 2-(4- fluorophenyl)-lH-imidazo[4,5-f][1,10]phenanthroline), has been achieved under hydrothermal conditions. The structure of compound 1 was determined by single-crystal X-ray diffraction. Compound 1 crystallizes in monoclinic, space group P21/c with a = 8.944(2), b = 18.781(5), c = 10.904(3) A, β = 91.392(4)°, V = 1831.2(8) A^3, Z = 2, C3sH26Cd2F2C14Cl4N8O2, Mr = 1031.27, Dc = 1.870 g/cm3, F(000) = 1016, μ(MoKα) = 1.513 mm^-1, R = 0.0532 and wR = 0.1407. Each Cd(ll) atom is in an octahedral coordination sphere, completed by two nitrogen atoms from one L ligand, two chlorine anions, and one water oxygen atom. Two chlorine anions bridge two Cd(Ⅱ) atoms to give a dimer [Cd(Cl)2(L)(H2O)]2. Adjacent dimers are stacked by one type of π…π interactions among L ligands to generate a 1D supramolecular chain. Further, the 1D supramolecular chains are stacked by another type of π…π interactions among L ligands to give a 2D supramolecular layer. Finally, the luminescent property of 1 has been studied in solid state at room temperature.
基金Supported by the Institute Foundation of Siping City(No.2009011)
文摘A novel Fe(II) coordination polymer [Fe(L)(trans-1,4-chdc)];~ has been hydrother- mally synthesized by using 1,4-cyclohexanedicarboxylic acid (1,4-H2chdc) and 2-(2-fluoro- phenyl)-lH-imidazo[4,5-f][1,10]phenanthroline (L). Crystallographic data: monoclinic, space group C2/c with a = 14.571(5), b = 32.389(6), c = 10.948(5)A, 18 = 115.186(5)°, V= 4676(3)A3, Z = 8, C27H21FFeN404, Mr = 540.33, De --- 1.535 g/cm3, F(000) = 2224, μ(MoKa) = 0.697 mmI, R = 0.0462 and wR = 0.1110. The two kinds of trans-l,4-chdc ligands link neighboring Fe(II) atoms to yield a two-dimensional layer structure. The π-π interactions between the L ligands of neighboring layers result in a three-dimensional supramolecular architecture. The IR and UV-vis spectra of the compound have been investigated in detail.
基金Supported by Jilin Province Science and Technology Development projects (No. 20100549)
文摘A new 1D coordination polymer, [Pb(L)(cis-1,4-chdc)]·0.5H2O (cis-1,4-chdc = 1,4-cyclohexanedicarboxylate and L = 2-(4-fluorophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline), has been synthesized under hydrothermal conditions and characterized by elemental analysis, TG and single-crystal X-ray diffraction. It crystallizes in triclinic, space group P1 with a = 9.153(5), b = 10.338(5), c = 13.074(5), α = 80.956(5), β = 89.725(5), γ = 80.534(5)°, V = 1204.8(10)3 , Z = 1, C54H44F2N8O9Pb2 , Mr = 1401.35, Dc = 1.931 g/cm3 , F(000) = 678, μ(MoKa) = 7.055 mm-1 , R = 0.0277 and wR = 0.0559. Each cis-1,4-chdc anion coordinates with two Pb(Ⅱ) atoms in a bis-chelating coordination mode. In this way, cis-1,4-chdc anions bridged the neighboring Pb(Ⅱ) atoms to generate a 1D chain structure. The L ligands from neighboring chains are paired through the strong π-π interactions to generate a fascinating 2D supramolecular layer.
基金Supported by the Institute Foundation of Siping City (No. 2009011)
文摘A new one-dimensional Ni(Ⅱ) coordination polymer [Ni(L)(cis-1,4- chdc)]n·1.25nH2O has been synthesized under hydrothermal conditions by using 1,4-cyclohexanedicarboxylic acid (1,4-H2chdc) and 2-(3-fluorophenyl)- 1H-imidazo [4,5-f] [ 1,10]phenanthroline (L). Crystallographic data for the compound: triclinic, space group Pi with a = 8.777(2), b = 10.662(2), c = 13.799(3) A, a = 89.480(4), β = 73,933(3), γ = 81.980(4)°, V = 1228.2(5) A3, Z = 2, C27H22.50FN4NiO5.25, Mr = 568.70, Dc = 1.527 g/cm3, F(000) = 583,μ(MoKα) = 0.846 mm-1, R = 0.0634 and wR = 0.1465. Neighboring Ni(Ⅱ) atoms are linked by the cis-1,4-chdc ligands to generate a one-dimensional chain structure. The π-π interactions between the L ligands of neighboring chains led to the formation of a two-dimensional supramolecular layer. The elemental analysis, IR spectrum and TG of the compound have been studied.
基金Supported by the Institute Foundation of Siping City (No. 2009011)
文摘The title coordination polymer, [Pb(L)(1,4-ndc)] 1 (L = 2-(4-fluorophenyl)-1Himidazo[4,5f1,10]phenanthroline, 1,4-ndc = naphthalene-1,4-dicarboxylic acid), has been obtained by using hydrothermal synthesis and characterized by elemental analysis, IR and singlecrystal X-ray diffraction. It crystallizes in monoclinic, space group P21/c with a = 10.1043(11), b = 14.3162(15), c = 17.6061(18), β = 95.3990(10)°, V = 2535.5(5)3, Z = 4, C31H17FN4O4Pb, Mr = 735.68, Dc = 1.927 g/cm3, F(000) = 1416, μ(MoKa) = 6.709 mm-1, R = 0.0201 and wR = 0.0489. The 1,4-ndc dianions link neighboring Pb(II) atoms in a bis-chelating mode, yielding a one-dimensional chain structure along the c axis. The C-H···π interactions between the carbon atom of L ligand and the benzene ring of 1,4-ndc lead the one-dimensional chains to form a two-dimensional supramolecular layer. The π-π interactions between L ligand and 1,4-ndc ligand make the two-dimensional layers generate a three-dimensional supramolecular architecture. Additionally, the N-H···O hydrogen bonds further stabilize the structure of 1.
基金supported financially by the National Natural Science Foundation of China(21271091)。
文摘A new ligand,2-(2-methoxynaphthyl)-1H-imidazo[4,5-f][1,10]phenanthroline(mnipH),was synthesized by the condensation of 2-methoxy-1-naphthaldehyde and 5,6-diamino-1,10-phenanthroline.Then three ionic copper(I)complexes were obtained through the reactions of[Cu(MeCN)4]ClO4,mnipH and the chelating diphosphine ligands with a molar ratio of 1:1:1.The photoluminescence and the corresponding luminescent mechanism of all copper(I)complexes in the solid state were investigated at room temperature.
基金Supported by the Institute Foundation of Siping City (No.2009011)
文摘A new Pb(Ⅱ) coordination polymer [Pb(L1)(L2)]·1.25H2O has been synthesized with 2-(4-fluorophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline (L1) and sebacic acid (H2L2) under hydrothermal conditions. Crystallographic data: triclinic, space group Pī with a=8.4890(17), b=12.471(3), c=14.604(3), α=67.04(3), β=74.08(3), γ=85.80(3)°, V=1368.0(5)3 , Z=1, C58H59F2N8O10.5Pb2 , Mr=1488.51, Dc=1.807g/cm3 , F(000)=729, μ(MoKa)=6.221mm-1 , R=0.0283 and wR=0.0564. The L2 dianions bridge neighboring Pb(Ⅱ) atoms to form a two-dimensional layer structure. The π-π interactions between the L1 ligands of neighboring layers led to a three-dimensional supramolecular architecture. The IR and TGA of the complex have been studied in detail.
基金Supported by Jilin Province Science and Technology Development Projects (No.No.201105085)the Science and Technology Research Projects of the Education Committee of Jilin Province (No.2013206)
文摘Complex [Zn(L)(SO4)]0.5H20 (L = 2-(2-chloro-6-fluorophenyl)-lH-imidazo[4,5- J][1,10]phenanthroline) has been synthesized under hydrothermal conditions. The compound was characterized by elemental analysis, IR, TG and single-crystal X-ray diffraction. It crystallizes in monoclinic, space group P21/n with a = 9.9916(7), b = 12.3834(9), c = 29.259(2) A, fl = 97.7720(10)°, V = 3587.0(4) A^3, Z = 2, C76H41CI4F4NI60952Zn2, Mr = 1734.91, Dc = 1.606 g/cm^3, F(000) = 1754, p(MoKa) = 0.959 mm-1, R = 0.0492 and wR = 0.1385. The asymmetric unit of 1 contains one Zn(lI) atom, two L ligands, one sulfate anion and half a water molecule. Each Zn(lI) atom is five-coordinated by four nitrogen atoms from two different L ligands and one sulfate oxygen atom in a tetragonal pyramidal coordination environment. The N-H'"O hydrogen bonds link the discrete structure of 1 into a 2D supramolecular architecture. The photoluminescent property of 1 has also been studied in the solid state at room temperature.
基金supported by 973 (2006CB932900)NNSFC (20571074)NSF of Fujian Province (2007J172)
文摘The title complex,[Zn(ip)2(H2O)2][ZnCl4]·H2O·2DMF 1(ip=imidazo[4,5-f][1,10] phenanthroline),has been synthesized via the slow evaporation of concentrated reaction solution at room temperature.It was characterized by single-crystal X-ray diffraction.Crystal data for C32H36Cl4N10O5Zn2:white prism,0.17mm×0.15mm×0.10mm,monoclinic,space group P2/c,a=11.928(8),b=9.868(6),c=16.520(11),β=104.879(12)°,V=1879(2)3,Z=2,Mr=913.25,Dc=1.614 g/cm3,F(000)=932,μ=1.616 mm-1,λ(MoKα)=0.71073,GOOF=1.045,R=0.0710 and wR=0.1755 for 3055 observed reflections with I 〉 2σ(I). X-ray diffraction study reveals that the title complex has an interesting 3D architecture via hydrogen bonding interactions and π-π interactions. The IR, TGA, XRD and luminescent properties of complex 1 were also studied.