A novel coordination polymer [Cu(3-cpoa)(phen)(H2O)]n (3-cpoa2-=3-carboxyl phenoxyacetate, phen=1,10-phenanthroline) was synthesized and characterized by e lemental analysis, IR spectra and single crystal X-ray diffra...A novel coordination polymer [Cu(3-cpoa)(phen)(H2O)]n (3-cpoa2-=3-carboxyl phenoxyacetate, phen=1,10-phenanthroline) was synthesized and characterized by e lemental analysis, IR spectra and single crystal X-ray diffraction. Crystallogra phic facts are as follows: monoclinic crystal system, space group P21/n, a=0.688 96(14) nm, b=1.652 3(3) nm, c=1.651 1(3) nm, 穋m-3, F(000)=932, -ligands, two nitrogen atoms of 1,10-phen ligand and one coordinated water molecule. The copper atoms are bridged by 3-cp oa2-ligand, forming a one-dimensional chain along c axis. The distance of adjac ent Cu...Cu is 0.916 6(4) nm. A three-dimensional network structure is construct ed by the intermolecular hydrogen bond and stacking interactions. CCDC: 21972 4.展开更多
One-dimensional cyanide-bridged bimetallic coordination polymer [CuL(H 2O) 2] n [(CuL)·(μ-CN) 2Fe(CN) 4] 2n ·(H 2O) 2n was synthesized and structurally characterized. The coordination polymer crystallizes i...One-dimensional cyanide-bridged bimetallic coordination polymer [CuL(H 2O) 2] n [(CuL)·(μ-CN) 2Fe(CN) 4] 2n ·(H 2O) 2n was synthesized and structurally characterized. The coordination polymer crystallizes in a monoclinic system of the space group C2/c with a=2.983 1(5) nm, b=1.527 4(3) nm, c= 1.725 3(4) nm, β=107.68(2)°, V=7.490(3) nm3, Z=8, D c=1.382 g/cm3, F(000)=3 260, R=0.059 3, wR 2=0.132 3, S=0.885. The one-dimensional zigzag chain extents through Cu—CN—Fe—CN—Cu linkages. The adjacent two polymer chains are linked by the O—H……NC hydrogen bonding between [CuL(H 2O) 2] 2+ and [Fe(CN) 6] 3- ions to form hydrophilic channels in which water molecules are included.展开更多
A novel nickel(II) complex with 2,4-dihydroxybenzalidene benzoylhydrazone a nd pyridine ligands, Ni(C14H10N2O3)(C5H5N), has been synthesized and characteriz ed by elemental analysis and IR. The crystal structure of th...A novel nickel(II) complex with 2,4-dihydroxybenzalidene benzoylhydrazone a nd pyridine ligands, Ni(C14H10N2O3)(C5H5N), has been synthesized and characteriz ed by elemental analysis and IR. The crystal structure of the title complex has been determined by single crystal X-ray diffraction techniques. The crystal belo ngs to orthorhombic, space group Pbca. The cell parameters are: a=1.580 20(19) n m, b=1.362 18(16) nm, c=1.616 50(19) nm, and V=3.479 5(7) nm3, Z=8, Dc=1.497 Mg ·m-3, composed of two oxygen atoms, one n itrogen atom of tridentate acyhydrazone schiff base ligand and one nitrogen atom of the pyridine ligand. The analysis of the crystal structure indicates that th e complex has a one-dimensional chain structure, which is formed by intermolecul ar hydrogen bonds. CCDC: 244668.展开更多
The novel copper(Ⅱ)complex with 2-oxo-propionic acid benzoyl hydrazone and pyridine ligands, Cu(C10H8N2O3)·(C5H5N)·(H2O) (C10H8N2O32- is the dinegative ion of 2-oxo-propionicacid benzoyl hydrazone), has bee...The novel copper(Ⅱ)complex with 2-oxo-propionic acid benzoyl hydrazone and pyridine ligands, Cu(C10H8N2O3)·(C5H5N)·(H2O) (C10H8N2O32- is the dinegative ion of 2-oxo-propionicacid benzoyl hydrazone), has been synthesized and characterized by elemental analysis and IR. The crystal structure of the title complex was determined by single crystal X-ray diffraction technique. Complex crystallized in the triclinic space group P1 with a = 0.729 08(10) nm, b = 1.020 01(14) nm, c = 1.126 28(15) nm, α = 71.644(2) °, β = 80.437(2) °, γ = 89.160(2)°, V = 0.783 28(18) nm3, Z = 2, Dc = 1.547 Mg·m-3, μ(MoKa) = 1.417 mm-1, F(000) = 374. The final R1 = 0.030 6, wR2 = 0.084 2 for 2 992 observed reflections out of 3 357 unique reflections. In this complex, copper(Ⅱ)ion is square-pyramidally coordinated by two oxygen atoms and one nitrogen atom of tridentate C10H8N2O32- ligand, one nitrogen atom of the pyridine ligand, and one oxygen atom of water molecule with the oxygen atom of water molecule locating at the apical position. The analysis of the crystal structure indicates that the complex has a one-dimensional chain structure, which is formed by intermolecular hydrogen bonds. CCDC: 222656.展开更多
The title complex [La(DMSO)3(H2O)3Cr(CN)6]H2O was obtained by the reaction of LaCl37H2O, DMSO and K3[Cr(CN)6] in aqueous solution on a hot water bath. The crystal crystallizes in orthorhombic, space group P212121 with...The title complex [La(DMSO)3(H2O)3Cr(CN)6]H2O was obtained by the reaction of LaCl37H2O, DMSO and K3[Cr(CN)6] in aqueous solution on a hot water bath. The crystal crystallizes in orthorhombic, space group P212121 with a = 9.827(3), b = 15.037(4), c = 17.633(5) ? C12H26CrLaN6O7S3, Mr = 653.48, Z = 4, V = 2605.7(13) ?, Dc = 1.666 g/m3, (MoKa) = 2.314 mm-1, F(000) = 1300, R = 0.0205 and wR = 0.0481 for 5038 observed reflec- tions (I > 2s(I)). La3+ ion is eight-coordinated by three DMSO molecules, three H2O molecules and two [Cr(CN)6]3- units. The structure of the title complex possesses a cyano-bridged one- dimensional zigzag chain structure with alternating La(DMSO)3(H2O)3 and Cr(CN)6 moieties, which are linked by some hydrogen bonds to form a 3D network structure.展开更多
Three new mixed-ligand Fe(Ⅱ/Ⅲ) complexes [Fe2(μ2–btec)( μ2–H2btec)(phen)2(H2O)2]n (1), [Fe2(btec) (phen)2(H2O)4] (2), and {[Fe(o-pha)(phen)(H2O)]·H2O}n (3) (phen=1,10-phenanthroline, o-H2pha=o-phthalic acid...Three new mixed-ligand Fe(Ⅱ/Ⅲ) complexes [Fe2(μ2–btec)( μ2–H2btec)(phen)2(H2O)2]n (1), [Fe2(btec) (phen)2(H2O)4] (2), and {[Fe(o-pha)(phen)(H2O)]·H2O}n (3) (phen=1,10-phenanthroline, o-H2pha=o-phthalic acid, H4btec=1,2,4,5-benzenetetracarboxylic acid) have been hydrothermally synthesized and detected by single crystal X-ray diffraction, showing that complexes (1) and (2) are both bridged by the betc4? ligands to form 1D chain and dinuclear structure and complex (3) is bridged by the o-pha groups to form 1D chain structure. The coordinated modes of the carboxyl groups adopt μ2-η1η1ηη1η1 and μ2-η2η1 respectively in complexes (2) and (3). The betc groups in complex (1) show two different coordinated modes: μ2-η1η1η1η1 and μ2-η1η1. In addition, the hydrogen bonds and π…π type interactions make the complex molecule further connect to three-dimensional and two-dimensional networks respectively. These complexes are detected by IR, UV-Vis-NIR and surface photovoltage spectrum (SPS). The SPS of complexes (1)–(3) indicate that there are positive SPV responses in the range of 300–600 nm and show p-type semiconductor characteristic. Because the structure, the valence and the coordinative environment of the Fe ions are all different in the three complexes, the intensity, position and the number of the response bands are different obviously. The results of SPS are corresponding with UV-Vis-NIR spectra.展开更多
文摘A novel coordination polymer [Cu(3-cpoa)(phen)(H2O)]n (3-cpoa2-=3-carboxyl phenoxyacetate, phen=1,10-phenanthroline) was synthesized and characterized by e lemental analysis, IR spectra and single crystal X-ray diffraction. Crystallogra phic facts are as follows: monoclinic crystal system, space group P21/n, a=0.688 96(14) nm, b=1.652 3(3) nm, c=1.651 1(3) nm, 穋m-3, F(000)=932, -ligands, two nitrogen atoms of 1,10-phen ligand and one coordinated water molecule. The copper atoms are bridged by 3-cp oa2-ligand, forming a one-dimensional chain along c axis. The distance of adjac ent Cu...Cu is 0.916 6(4) nm. A three-dimensional network structure is construct ed by the intermolecular hydrogen bond and stacking interactions. CCDC: 21972 4.
文摘One-dimensional cyanide-bridged bimetallic coordination polymer [CuL(H 2O) 2] n [(CuL)·(μ-CN) 2Fe(CN) 4] 2n ·(H 2O) 2n was synthesized and structurally characterized. The coordination polymer crystallizes in a monoclinic system of the space group C2/c with a=2.983 1(5) nm, b=1.527 4(3) nm, c= 1.725 3(4) nm, β=107.68(2)°, V=7.490(3) nm3, Z=8, D c=1.382 g/cm3, F(000)=3 260, R=0.059 3, wR 2=0.132 3, S=0.885. The one-dimensional zigzag chain extents through Cu—CN—Fe—CN—Cu linkages. The adjacent two polymer chains are linked by the O—H……NC hydrogen bonding between [CuL(H 2O) 2] 2+ and [Fe(CN) 6] 3- ions to form hydrophilic channels in which water molecules are included.
文摘A novel nickel(II) complex with 2,4-dihydroxybenzalidene benzoylhydrazone a nd pyridine ligands, Ni(C14H10N2O3)(C5H5N), has been synthesized and characteriz ed by elemental analysis and IR. The crystal structure of the title complex has been determined by single crystal X-ray diffraction techniques. The crystal belo ngs to orthorhombic, space group Pbca. The cell parameters are: a=1.580 20(19) n m, b=1.362 18(16) nm, c=1.616 50(19) nm, and V=3.479 5(7) nm3, Z=8, Dc=1.497 Mg ·m-3, composed of two oxygen atoms, one n itrogen atom of tridentate acyhydrazone schiff base ligand and one nitrogen atom of the pyridine ligand. The analysis of the crystal structure indicates that th e complex has a one-dimensional chain structure, which is formed by intermolecul ar hydrogen bonds. CCDC: 244668.
文摘The novel copper(Ⅱ)complex with 2-oxo-propionic acid benzoyl hydrazone and pyridine ligands, Cu(C10H8N2O3)·(C5H5N)·(H2O) (C10H8N2O32- is the dinegative ion of 2-oxo-propionicacid benzoyl hydrazone), has been synthesized and characterized by elemental analysis and IR. The crystal structure of the title complex was determined by single crystal X-ray diffraction technique. Complex crystallized in the triclinic space group P1 with a = 0.729 08(10) nm, b = 1.020 01(14) nm, c = 1.126 28(15) nm, α = 71.644(2) °, β = 80.437(2) °, γ = 89.160(2)°, V = 0.783 28(18) nm3, Z = 2, Dc = 1.547 Mg·m-3, μ(MoKa) = 1.417 mm-1, F(000) = 374. The final R1 = 0.030 6, wR2 = 0.084 2 for 2 992 observed reflections out of 3 357 unique reflections. In this complex, copper(Ⅱ)ion is square-pyramidally coordinated by two oxygen atoms and one nitrogen atom of tridentate C10H8N2O32- ligand, one nitrogen atom of the pyridine ligand, and one oxygen atom of water molecule with the oxygen atom of water molecule locating at the apical position. The analysis of the crystal structure indicates that the complex has a one-dimensional chain structure, which is formed by intermolecular hydrogen bonds. CCDC: 222656.
基金This work was supported by the National Natural Science Foundation of China (No. 50242001)
文摘The title complex [La(DMSO)3(H2O)3Cr(CN)6]H2O was obtained by the reaction of LaCl37H2O, DMSO and K3[Cr(CN)6] in aqueous solution on a hot water bath. The crystal crystallizes in orthorhombic, space group P212121 with a = 9.827(3), b = 15.037(4), c = 17.633(5) ? C12H26CrLaN6O7S3, Mr = 653.48, Z = 4, V = 2605.7(13) ?, Dc = 1.666 g/m3, (MoKa) = 2.314 mm-1, F(000) = 1300, R = 0.0205 and wR = 0.0481 for 5038 observed reflec- tions (I > 2s(I)). La3+ ion is eight-coordinated by three DMSO molecules, three H2O molecules and two [Cr(CN)6]3- units. The structure of the title complex possesses a cyano-bridged one- dimensional zigzag chain structure with alternating La(DMSO)3(H2O)3 and Cr(CN)6 moieties, which are linked by some hydrogen bonds to form a 3D network structure.
基金supported by the National Natural Science Foundation of China (Grant No. 20571037)Liaoning Province Foundation (Grant No. 2007T092)
文摘Three new mixed-ligand Fe(Ⅱ/Ⅲ) complexes [Fe2(μ2–btec)( μ2–H2btec)(phen)2(H2O)2]n (1), [Fe2(btec) (phen)2(H2O)4] (2), and {[Fe(o-pha)(phen)(H2O)]·H2O}n (3) (phen=1,10-phenanthroline, o-H2pha=o-phthalic acid, H4btec=1,2,4,5-benzenetetracarboxylic acid) have been hydrothermally synthesized and detected by single crystal X-ray diffraction, showing that complexes (1) and (2) are both bridged by the betc4? ligands to form 1D chain and dinuclear structure and complex (3) is bridged by the o-pha groups to form 1D chain structure. The coordinated modes of the carboxyl groups adopt μ2-η1η1ηη1η1 and μ2-η2η1 respectively in complexes (2) and (3). The betc groups in complex (1) show two different coordinated modes: μ2-η1η1η1η1 and μ2-η1η1. In addition, the hydrogen bonds and π…π type interactions make the complex molecule further connect to three-dimensional and two-dimensional networks respectively. These complexes are detected by IR, UV-Vis-NIR and surface photovoltage spectrum (SPS). The SPS of complexes (1)–(3) indicate that there are positive SPV responses in the range of 300–600 nm and show p-type semiconductor characteristic. Because the structure, the valence and the coordinative environment of the Fe ions are all different in the three complexes, the intensity, position and the number of the response bands are different obviously. The results of SPS are corresponding with UV-Vis-NIR spectra.
