A one dimension solid and a two dimension solid consisting of polyoxoanions bridged by {CoO 3N 2} and {CoO 4} groups respectively have been synthesized by the hydrothermal method and structurally characterized by...A one dimension solid and a two dimension solid consisting of polyoxoanions bridged by {CoO 3N 2} and {CoO 4} groups respectively have been synthesized by the hydrothermal method and structurally characterized by X Ray crystallography. Each structure has the [(PO 4) 4Mo 6O 15 ] 12- cluster that is commonly observed in many molybdophosphates. In compound 1, [(PO 4) 4Mo 6O 15 ] 12- clusters are linked by {CoO 3N 2} groups to form a chain like structure, and the chains are hydrogen bonded into a network. Compound 2 is a layer structure with channnels constructed from [(PO 4) 4Mo 6O 15 ] 12- clusters and {CoO 4} groups, the organic molecules and the lattice water molecules are distributed disorderly in the interlamellar region and form strong hydrogen bonds with inorganic framework. The IR and the fluorescent spectra were investigated and discussed.展开更多
The self-assembly of a flexible bipyridyl ligand 2,2?-bis(4-pyridylmethyle- neoxy)-1,1?-biphenylene (4,4?-bpp) with cobalt(II) center gave rise to a one-dimensional chain complex [Co(μ-4,4?-bpp)2(SCN)2?H2O]n 1 which ...The self-assembly of a flexible bipyridyl ligand 2,2?-bis(4-pyridylmethyle- neoxy)-1,1?-biphenylene (4,4?-bpp) with cobalt(II) center gave rise to a one-dimensional chain complex [Co(μ-4,4?-bpp)2(SCN)2?H2O]n 1 which has been characterized by single-crystal X-ray diffraction. The polymer crystallizes in monoclinic, space group C2/c with unit cell parameters: a = 13.1888(13), b = 24.230(2), c = 15.4218(17) ?, β = 93.291(6)o, V = 4920.1(8) ?3, Z = 4, C50H42CoN6O5S2, Mr = 929.95, Dc = 1.255 g/cm3, F(000) = 1932 and μ(MoKα) = 0.484 mm-1. The final R and wR are 0.0691 and 0.1670 for 3746 observed reflections with I > 2σ(I). 1 possesses an infinite 1-D polymeric chain structure consisting of the repeated basic square units Co2(μ-4,4?-bpp)2, where the Co(II) center acts as the joint of the square ring. The Co(II) center is coordinated in a slightly distorted octahedral geometry with four nitrogen atoms from four different 4,4?-bpp ligands in the equatorial plane and two trans thiocyanate ligands occupying the axial positions, preventing the formation of an extended framework.展开更多
High diffraction quality crystals of cucurmosin, a type I ribosome inactivating protein isolated from the sarcocarp of Cucurbita moschata (pumpkin), have been grown under newly optimised conditions. With in-house rota...High diffraction quality crystals of cucurmosin, a type I ribosome inactivating protein isolated from the sarcocarp of Cucurbita moschata (pumpkin), have been grown under newly optimised conditions. With in-house rotating anode X-ray source, these crystals diffract to 1.65 ?resolution which is much higher than that of the previously reported crystals that diffracted only to 3 ?resolution. The crystals belong to space group P212121 with cell parameters a = 41.5, b = 58.4 and c = 99.3 . Molecular replacement studies indicate that the cucurmosin structure is homologous to trichosanthin. The initial structural model has been obtained and the model fitting/ refinement is in progress.展开更多
The title complex, [Cu(L)Cl2]n (L = 2,5-di-2-pyridyl-1,3,4-oxodiazole) 1, has been obtained from the reaction of 3,6-di-2-pyridyl-1,2,4,5-tetrazine (bptz) and CuCl2?H2O in a mixture solvent of CH3CN and CH2Cl2 (L is g...The title complex, [Cu(L)Cl2]n (L = 2,5-di-2-pyridyl-1,3,4-oxodiazole) 1, has been obtained from the reaction of 3,6-di-2-pyridyl-1,2,4,5-tetrazine (bptz) and CuCl2?H2O in a mixture solvent of CH3CN and CH2Cl2 (L is generated from the metal-assisted hydrolysis reaction of bptz) and structurally characterized. It crystallizes in space group C2/c of monoclinic system with cell parameters: a = 9.812(2), b = 12.679(3), c = 11.111(2) ? b = 103.92(3)? V = 1341.6(5) 3, Z = 4, Dc = 1.776 g/cm3, Mr = 358.66, F(000) = 716, ?= 2.024 mm1 and S = 1.004. The final R = 0.0346 and wR = 0.0938 for 1011 observed reflections with I > 2(I). The Cu(Ⅱ) ion is six-coordinated by four N atoms of two L ligands and two Cl ions in a distorted octahedral geometry. The ligand L acts as a bis-bidentate ligand to bridge the Cu(Ⅱ) ions, resulting in an infinite chain structure.展开更多
The title complex [Cu2(bipy)2(Hpht)2Cl](Hpht) (bipy = 2,2?-bipyridine, H2pht = o-phthalic acid) has been synthesized in the NaOH aqueous solution of CuCl2, Gd(NO3)3, bipy and H2pht, and its crystal structure was det...The title complex [Cu2(bipy)2(Hpht)2Cl](Hpht) (bipy = 2,2?-bipyridine, H2pht = o-phthalic acid) has been synthesized in the NaOH aqueous solution of CuCl2, Gd(NO3)3, bipy and H2pht, and its crystal structure was determined by single-crystal X-ray diffraction method. It crys- tallizes in triclinic, space group P1, C44H31ClCu2N4O12, Mr = 970.26, a = 8.175(2), b = 16.254(4), c = 16.946(4) ?, α = 62.966(6), β = 84.833(8), γ = 84.348(8)°, V = 1993.4(8) ?3, Z = 2, Dc = 1.616 g/cm3, F(000) = 988 and μ = 1.207 mm-1. The final R = 0.0429 and wR = 0.0843 for 5682 observed reflections with I > 2σ(I). Each copper(II) atom displays a distorted square-pyramidal geometry with two nitrogen atoms of one chelate 2,2?-bipy molecule, two oxygen atoms from two different bridging carboxylate groups of Hpht- and one bridging chloride atom occupying the apical position. The two copper(II) atoms are connected by a μ2-Cl atom and two bridging Hpht- ligands in a syn-syn coordination mode to form an isolated dinuclear unit. The molecular structure is extended to a one-dimensional wavy chain through hydrogen bonds. The title complex exhibits blue fluorescent emission at 443 nm (λex = 372 nm) in the solid state at room temperature.展开更多
MnCl2 (C12,H8N2)2, Mr= 486. 26, monoclinic, P21,/c, a= 9. 461 (5),b= 15. 20(1), c= 14. 514(2) A, β=98. 82(3)°, V=2062(2) A3, Z=4, Dc= 1. 57g/cm3. λ(MoKα) = 0. 71073 A, μ(MoKα) = 0. 895 mm-l, F (000) = 988, T...MnCl2 (C12,H8N2)2, Mr= 486. 26, monoclinic, P21,/c, a= 9. 461 (5),b= 15. 20(1), c= 14. 514(2) A, β=98. 82(3)°, V=2062(2) A3, Z=4, Dc= 1. 57g/cm3. λ(MoKα) = 0. 71073 A, μ(MoKα) = 0. 895 mm-l, F (000) = 988, T= 296K. Final R= 0. 043, Rw= 0. 053 for 2569 observed reflections. The Mn atom is co-ordinated by two Cl anions and four N of two phenanthroline (phen) molecules, forming a distorted octahedron. Two Mn--Cl bond lengths are 2. 437(2) and 2. 449(2) A,respectively. The Mn--N bond lengths vary from 2. 290(3) to 2. 367 (4) A。 The dihedral angle between two phen best planes is 90. 4°.展开更多
The title complex NiL(py)3, where H2L = N-salicylaldehyde-N-phenoxyacetyl hydrazine, was prepared and characterized by X-ray diffraction. The single crystal of the title compound, Ni(C15H12N2O3)(C5H5N)3, is of monocli...The title complex NiL(py)3, where H2L = N-salicylaldehyde-N-phenoxyacetyl hydrazine, was prepared and characterized by X-ray diffraction. The single crystal of the title compound, Ni(C15H12N2O3)(C5H5N)3, is of monoclinic, space group P21/c with a = 11.900(1), b = 9.6855(7), c = 23.658(2) , b = 92.357(2)? V = 2724.5(4) 3, Z = 4, F(000) = 1176, Dc = 1.376 g/cm3, ?= 0.753 mm-1, R = 0.0332 and wR = 0.0820. The coordination polyhedron around the nickel atom is an elongated octahedron. The basal plane consists of one phenol oxygen, one amine carbonyl oxygen and one hydrazine nitrogen atoms from the ligand L2- and one nitrogen atom from one coordinated pyridine ligand, while the axial sites are occupied by two nitrogen atoms of two coordinated pyridine ligands.展开更多
Two mononuclear tin(IV) complexes, [Sn(pda)2(edt)2] (pda = o-phenylenediamine) (C16H24N4S4Sn, Mr = 519.32) 1 and [Sn(eda)(edt)2] (eda = ethylenediamine) (C6H16N2S4Sn, Mr = 363.14) 2 were synthesized and characterized ...Two mononuclear tin(IV) complexes, [Sn(pda)2(edt)2] (pda = o-phenylenediamine) (C16H24N4S4Sn, Mr = 519.32) 1 and [Sn(eda)(edt)2] (eda = ethylenediamine) (C6H16N2S4Sn, Mr = 363.14) 2 were synthesized and characterized by X-ray structure analysis. 1 belongs to trigonal, space group P-3c1 with a = b = 20.0280(6), c = 8.7679(5) ? V = 3045.8(2) ?, Z = 6, Dc = 1.699 g/cm3, m = 1.677 mm-1, F(000) = 1572, the final R = 0.0418 and wR = 0.1019 for 1805 independent reflections. 2 crystallizes in monoclinic, space group P21/c with a = 10.911(3), b = 9.783(2), c = 11.831(3) ? b = 100.28(2), V = 1242.6(6) ?, Z = 4, Dc = 1.941 g/cm3, m = 2.690 mm-1, F(000) = 720, the final R = 0.0280 and wR = 0.0627 for 2166 independent reflections. Both Sn4+ ions in these two complexes are six-coordinated with a slightly distorted octahedral configu- ration.展开更多
The spectral parameters of Nd3+ ions in Nd3+:Klu(WO4)2 crystal were calculated based on Judd-Ofelt theory and obtained as follows: for the oscillator strengths ?λ: ?2 = 7.5029×10-20 cm2, ?4 = 7.1837×10-20...The spectral parameters of Nd3+ ions in Nd3+:Klu(WO4)2 crystal were calculated based on Judd-Ofelt theory and obtained as follows: for the oscillator strengths ?λ: ?2 = 7.5029×10-20 cm2, ?4 = 7.1837×10-20 cm2 and ?6 = 3.1189×10-20 cm2; the radiative lifetime is 123 μs; the quantum efficiency is equal to 64.55%; and β1 = 0.5498, β2 = 0.3943, β3 = 0.0551 and β4 = 0.0027 for the fluorescence branch ratios.展开更多
The hydro(solvo)thermal reactions of cobalt powder or its chloride with 2,5- pyridine dicarboxylic acid (H2PYDC) yielded two new complexes: [Co(II)2(PYDC)2(H2O)2- (H2O)4]n 1 and {Co(II)[NH2(CH3)2]2(PYDC)2}n 2. It is o...The hydro(solvo)thermal reactions of cobalt powder or its chloride with 2,5- pyridine dicarboxylic acid (H2PYDC) yielded two new complexes: [Co(II)2(PYDC)2(H2O)2- (H2O)4]n 1 and {Co(II)[NH2(CH3)2]2(PYDC)2}n 2. It is observed that the reactive solvents result in different connectivity modes of ligand and diverse dimensional extension of crystal structures. The correlation between structure and magnetic property will be discussed in this paper. Crystal data for 1: space group P1, a = 7.0419(17), b = 8.937(2), c = 9.6182(19) ?, α = 91.532(4), β = 99.869(10), γ = 107.889(11)o, V = 565.5(2) ?3, Z = 1, Dc = 1.845 g/cm3, μ = 1.56 mm-1, F(000) = 322 , R = 0.0505 and wR = 0.1580; and those for 2: space group C2/c, a = 14.9075(6), b = 8.2523(3), c = 16.9643(2) ?, β = 100.982(2)o, V = 2048.75(11) ?3, Z = 4, Dc = 1.560 g/cm3, μ = 0.892 mm-1, F(000) = 996, R = 0.0443 and wR = 0.1134.展开更多
The crystal structure of the title compound {[Mn(phen)2(OAc)(H2O)]ClO4}2H2O (phen = 1,10-phenanthroline) has been synthesized and determined by X-ray diffraction. The crystal is of triclinic, space group P?with a = 12...The crystal structure of the title compound {[Mn(phen)2(OAc)(H2O)]ClO4}2H2O (phen = 1,10-phenanthroline) has been synthesized and determined by X-ray diffraction. The crystal is of triclinic, space group P?with a = 12.7955(4), b = 15.0544(4), c = 16.2183(4) , ?= 64.479(1), b =67.526(1), g = 83.582(1), C52H40Cl2Mn2N8O15, Mr = 1197.70, V = 2600.1(1) ?, Dc = 1.530 g/cm3, F(000) = 1224, = 0.666 cm-1 and Z = 2. The final refinement gave R = 0.0691 and wR = 0.1821 for 6131 observed reflections with I > 2s(I). The cell of the complex contains two uniform mono-manganese molecules [Mn(phen)2(OAc)(H2O)]ClO4 and a solvate water molecule. Four nitrogen atoms from two chelating phenanthroline ligands and one oxygen atom from acetate ligate to the MnⅡ ion, forming a distorted octahedral geometry together with one coordinated water molecule. One ClO4- anion and one water molecule exist outside the cation [Mn(phen)2(OAc)- (H2O)]+ as a counter ion and solvate molecule, respectively.展开更多
[Mo3S4(μ-CH3COO)[S2P(OEt)2]3(py)]·(CH3COOCH2CH3) , Mr = 1197. 96,monoclinic,P21/n,a=13. 158(2),b=23. 153(5), c=16. 175(3) A,β = 112. 79(1)°,V=4543. 1(7)A3,Z=4, Dc= 1. 751g/cm-3,λ(MoKa) = 0. 71073A ,μ= 13...[Mo3S4(μ-CH3COO)[S2P(OEt)2]3(py)]·(CH3COOCH2CH3) , Mr = 1197. 96,monoclinic,P21/n,a=13. 158(2),b=23. 153(5), c=16. 175(3) A,β = 112. 79(1)°,V=4543. 1(7)A3,Z=4, Dc= 1. 751g/cm-3,λ(MoKa) = 0. 71073A ,μ= 13. 799cm-1,F(000) = 2408. Final R=0. 067 for 4000 reflections. The structure consists of the neutral cluster molecule [Mo3S4(μ-OAc) (dtp)3(py)] (dtp = [S2P(OEt)2]) and the solvent ethyl acetate (AcOEt). The three Mo-Mo bond lengths in the title compound are 2. 691(2) ,2. 747(2) ,2. 762(2) A ,whereas the Mo-N bond length in Mo(3) position is 2. 36(2)A. The important bond lengths of these Mo clusters with (py) ring at the loose coordination site are listed for comparison.展开更多
The title complex [Cu3L3(H2O)]DMFH2O (H2L = 4-(3-hydroxy-2-ethyl-4- pyridinone-1-yl)-aniline condensation salicylaldehyde) was obtained. The single-crystal X-ray study shows that it is a trinuclear compound [Cu3(C20H1...The title complex [Cu3L3(H2O)]DMFH2O (H2L = 4-(3-hydroxy-2-ethyl-4- pyridinone-1-yl)-aniline condensation salicylaldehyde) was obtained. The single-crystal X-ray study shows that it is a trinuclear compound [Cu3(C20H15N2O3)3(H2O)]DMFH2O. The coordi- nation sphere about each copper ion in the complex consists of two oxygen atoms from hydroxylpyridinone moiety of one ligand and one oxygen and one nitrogen atoms from salicyladehyde Schiff-base moiety of another ligand arranged in a slightly distorted square planar geometry. Among the three copper ions, one (Cu(2)) is coordinated by the other oxygen atom of water molecule on the fifth coordinate position to form a distorted square pyramid geometry. The crystal is of monoclinic, space group P21/c with a = 12.9202(5), b = 27.197(1), c = 17.0116(7) ? b = 100.588(1), V = 5875.9(4) 3, Z = 4, C63H57N7O12Cu3, Mr = 1294.78, Dc = 1.464 g/cm3, m = 1.146 mm-1, F(000) = 2668, R = 0.0784 and wR = 0.1546 for 6926 observed reflections with I > 2s(I). The differences of coordinate bond lengths are observed between anhydrous and hydrous units: in the former unit, the average bond lengths are 1.978 ?for CuN (azomethine), 1.883 ?for CuO (phenolic) in Schiff-base moiety, 1.959 ?for CuO (keto), and 1.919 ?for CuO (hydroxy) in hydroxypyridinone moiety; while those in the latter are longer with the following corresponding values: 1.985(5), 1.908(5), 1.993(5) and 1.919(4) ? respectively. The Cu(2)O (water) bond length is 2.375(6) ?展开更多
A two-dimensional hydrogen-bonded cadmium(II) compound [Cd(dapm)2- (CH3COO)2(H2O)2] (dapm = diaminodiphenylmethane) has been synthesized and characterized by single-crystal X-ray diffraction analysis. It crystallizes ...A two-dimensional hydrogen-bonded cadmium(II) compound [Cd(dapm)2- (CH3COO)2(H2O)2] (dapm = diaminodiphenylmethane) has been synthesized and characterized by single-crystal X-ray diffraction analysis. It crystallizes in monoclinic, space group C2/c with a = 27.572(3), b = 5.5064(5), c = 23.310(2) , = 124.785(1)o, C15H19Cdo.5ON2O3, Mr =331.52, V = 2906.6(5) ?, Z = 4, Dc = 1.515 g/cm3, F(000) = 1368 and = 0.801 mm-1. The final R = 0.0403 and wR = 0.1014 for 1795 observed reflections with I≥4(I). The centrosymmetric Cd(II) is six- coordinated in a distorted octahedral geometry, and the dapm in a trans mode acts as a monoden- tate ligand. The intermolecular hydrogen bonds among coordinated aqua molecules with coordi- nated acetate oxygen atoms and uncoordinated dapm nitrogen atoms form a two-dimensional supramolecular framework.展开更多
The crystal structures of two coordination polymers [Ln(IN)3(H2O)2]n (Ln = Nd 1, Gd 2; IN = isonicotinate) were determined by single-crystal X-ray diffraction and further chara- cterized by IR, elemental analysis and ...The crystal structures of two coordination polymers [Ln(IN)3(H2O)2]n (Ln = Nd 1, Gd 2; IN = isonicotinate) were determined by single-crystal X-ray diffraction and further chara- cterized by IR, elemental analysis and thermogravimetric analysis. Crystal data for 1: monoclinic, space group P21/c, a = 9.6636(5), b = 19.7532(10), c = 11.6183(6) ?, β = 112.032(1)°, V = 2055.83(18) ?3, Z = 4, Dc = 1.766 g/cm3, F(000) = 1076, μ = 2.575 mm–1 and R = 0.0493; Crystal data for 2: monoclinic, space group C2/c, a = 20.251(2), b = 11.6199(11), c = 9.8240(9) ?, β = 115.505(3)°, V = 2086.4(3) ?3, Z = 4, Dc = 1.781 g/cm3, F(000) = 1092, μ = 3.228 mm–1 and R = 0.0695. In the title compounds, the center atoms Ln(III) are in a distorted square antiprismatic geometry and linked by bridging isonicotinate to form an infinite chain. The intermolecular hydro- gen bonds lead to the formation of three-dimensional supramolecular structures.展开更多
A hydrothermal reaction of copper acetate with ammonium molybdate, 4,4-bpy (4,4-bipyridine) and 1,10-phen (1,10-phenanthroline) led to the formation of brown crystals of [Cu2(1,10-phen)2(4,4-bpy)]2 [Mo8O26]4H2O 1. Si...A hydrothermal reaction of copper acetate with ammonium molybdate, 4,4-bpy (4,4-bipyridine) and 1,10-phen (1,10-phenanthroline) led to the formation of brown crystals of [Cu2(1,10-phen)2(4,4-bpy)]2 [Mo8O26]4H2O 1. Single-crystal X-ray analysis has revealed that 1 (C68H56N12O30Cu4Mo8) crystallizes in the triclinic system, space group P with a = 11.270(3), b = 13.113(6), c = 13.906(3) ? = 103.33(4), b = 98.54(2), g = 101.29(2)? V = 1920.1(1) ?3, Mr = 2542.93, Z = 1, Dc = 2.199 g/cm3, m = 2.435 mm-1, F(000) = 1240, the final R = 0.0445, wR = 0.1082 and S = 1.021 for 5052 observed reflections with I >2s(I). It consists of copper (Ⅰ) tetramer units and -[Mo8O26]4- anions, which are further attached into a three-dimensional framework through hydrogen bonding and - stacking interactions.展开更多
A novel supramolecular adduct 3(C 42H 42N 28O 14) 2·H 2O (1) was synthesized by mixing 2- and cucurbit uril in solution of hydrochloric acid. The crystal structure was determined by single crys...A novel supramolecular adduct 3(C 42H 42N 28O 14) 2·H 2O (1) was synthesized by mixing 2- and cucurbit uril in solution of hydrochloric acid. The crystal structure was determined by single crystal X-ray diffraction analysis. The crystal belongs to orthorhombic system and space group F dd2 with cell dimensions: a=4.705 33 (5) nm, b=7.153 80 (6) nm, c= 1.894 61 (2) nm, Z=16, V=63.7744 (11) nm3, D c= 1.534 g/cm3, μ=3.007 mm -1, F(000)=29 120, R 1= 0.070 7, wR 2=0.169 2. In crystal, the cucurb uril molecules form two zig-zag chains.展开更多
Crystals of the low temperature phase b-Ba3Y(BO3)3 have been synthesized by the flux method. The structure of the title compound crystallizes in the hexagonal system, space group P63cm with the following parameters: a...Crystals of the low temperature phase b-Ba3Y(BO3)3 have been synthesized by the flux method. The structure of the title compound crystallizes in the hexagonal system, space group P63cm with the following parameters: a = 9.416(3), c = 17.536(8) ? V = 1346.6(8) ?, Ba3YB3O9, Mr = 677.36, Z = 6, Dc = 5.012 g/cm3, l(MoKa) = 0.71073 ? m = 19.409 mm-1, Flack parameter = 0.02(3), F(000) = 1764, R = 0.0714 and wR = 0.1696 for 1076 observed reflections with I > 2s(I). The compound contains two sets of YO6 octahedra, four sets of BaO9 polyhedra and three sets of BO3 planar triangles.展开更多
文摘A one dimension solid and a two dimension solid consisting of polyoxoanions bridged by {CoO 3N 2} and {CoO 4} groups respectively have been synthesized by the hydrothermal method and structurally characterized by X Ray crystallography. Each structure has the [(PO 4) 4Mo 6O 15 ] 12- cluster that is commonly observed in many molybdophosphates. In compound 1, [(PO 4) 4Mo 6O 15 ] 12- clusters are linked by {CoO 3N 2} groups to form a chain like structure, and the chains are hydrogen bonded into a network. Compound 2 is a layer structure with channnels constructed from [(PO 4) 4Mo 6O 15 ] 12- clusters and {CoO 4} groups, the organic molecules and the lattice water molecules are distributed disorderly in the interlamellar region and form strong hydrogen bonds with inorganic framework. The IR and the fluorescent spectra were investigated and discussed.
基金This work was supported by the National Natural Science Foundation of China (No. 20231020)
文摘The self-assembly of a flexible bipyridyl ligand 2,2?-bis(4-pyridylmethyle- neoxy)-1,1?-biphenylene (4,4?-bpp) with cobalt(II) center gave rise to a one-dimensional chain complex [Co(μ-4,4?-bpp)2(SCN)2?H2O]n 1 which has been characterized by single-crystal X-ray diffraction. The polymer crystallizes in monoclinic, space group C2/c with unit cell parameters: a = 13.1888(13), b = 24.230(2), c = 15.4218(17) ?, β = 93.291(6)o, V = 4920.1(8) ?3, Z = 4, C50H42CoN6O5S2, Mr = 929.95, Dc = 1.255 g/cm3, F(000) = 1932 and μ(MoKα) = 0.484 mm-1. The final R and wR are 0.0691 and 0.1670 for 3746 observed reflections with I > 2σ(I). 1 possesses an infinite 1-D polymeric chain structure consisting of the repeated basic square units Co2(μ-4,4?-bpp)2, where the Co(II) center acts as the joint of the square ring. The Co(II) center is coordinated in a slightly distorted octahedral geometry with four nitrogen atoms from four different 4,4?-bpp ligands in the equatorial plane and two trans thiocyanate ligands occupying the axial positions, preventing the formation of an extended framework.
基金Supported by the National Natural Science Foundation of China (39970872) NSF of Fujian province+1 种基金 and International Cooperation program of Fujian province to the State Key Laboratory of Structural Chemistry Fujian Institute of Research on the Struct
文摘High diffraction quality crystals of cucurmosin, a type I ribosome inactivating protein isolated from the sarcocarp of Cucurbita moschata (pumpkin), have been grown under newly optimised conditions. With in-house rotating anode X-ray source, these crystals diffract to 1.65 ?resolution which is much higher than that of the previously reported crystals that diffracted only to 3 ?resolution. The crystals belong to space group P212121 with cell parameters a = 41.5, b = 58.4 and c = 99.3 . Molecular replacement studies indicate that the cucurmosin structure is homologous to trichosanthin. The initial structural model has been obtained and the model fitting/ refinement is in progress.
基金This work was supported by the National Natural Science Foundation of China (No.20001007 20131020) Natural Science Foundation of the Chinese Academy of Sciences (KJCX2-H3) and Fujian province (2000F006)
文摘The title complex, [Cu(L)Cl2]n (L = 2,5-di-2-pyridyl-1,3,4-oxodiazole) 1, has been obtained from the reaction of 3,6-di-2-pyridyl-1,2,4,5-tetrazine (bptz) and CuCl2?H2O in a mixture solvent of CH3CN and CH2Cl2 (L is generated from the metal-assisted hydrolysis reaction of bptz) and structurally characterized. It crystallizes in space group C2/c of monoclinic system with cell parameters: a = 9.812(2), b = 12.679(3), c = 11.111(2) ? b = 103.92(3)? V = 1341.6(5) 3, Z = 4, Dc = 1.776 g/cm3, Mr = 358.66, F(000) = 716, ?= 2.024 mm1 and S = 1.004. The final R = 0.0346 and wR = 0.0938 for 1011 observed reflections with I > 2(I). The Cu(Ⅱ) ion is six-coordinated by four N atoms of two L ligands and two Cl ions in a distorted octahedral geometry. The ligand L acts as a bis-bidentate ligand to bridge the Cu(Ⅱ) ions, resulting in an infinite chain structure.
基金This work was supported by the National Natural Science Foundation of China (20001007 20131020)+1 种基金and Natural Science Foundation of Fujian Province (2003I031 A0420002)
文摘The title complex [Cu2(bipy)2(Hpht)2Cl](Hpht) (bipy = 2,2?-bipyridine, H2pht = o-phthalic acid) has been synthesized in the NaOH aqueous solution of CuCl2, Gd(NO3)3, bipy and H2pht, and its crystal structure was determined by single-crystal X-ray diffraction method. It crys- tallizes in triclinic, space group P1, C44H31ClCu2N4O12, Mr = 970.26, a = 8.175(2), b = 16.254(4), c = 16.946(4) ?, α = 62.966(6), β = 84.833(8), γ = 84.348(8)°, V = 1993.4(8) ?3, Z = 2, Dc = 1.616 g/cm3, F(000) = 988 and μ = 1.207 mm-1. The final R = 0.0429 and wR = 0.0843 for 5682 observed reflections with I > 2σ(I). Each copper(II) atom displays a distorted square-pyramidal geometry with two nitrogen atoms of one chelate 2,2?-bipy molecule, two oxygen atoms from two different bridging carboxylate groups of Hpht- and one bridging chloride atom occupying the apical position. The two copper(II) atoms are connected by a μ2-Cl atom and two bridging Hpht- ligands in a syn-syn coordination mode to form an isolated dinuclear unit. The molecular structure is extended to a one-dimensional wavy chain through hydrogen bonds. The title complex exhibits blue fluorescent emission at 443 nm (λex = 372 nm) in the solid state at room temperature.
文摘MnCl2 (C12,H8N2)2, Mr= 486. 26, monoclinic, P21,/c, a= 9. 461 (5),b= 15. 20(1), c= 14. 514(2) A, β=98. 82(3)°, V=2062(2) A3, Z=4, Dc= 1. 57g/cm3. λ(MoKα) = 0. 71073 A, μ(MoKα) = 0. 895 mm-l, F (000) = 988, T= 296K. Final R= 0. 043, Rw= 0. 053 for 2569 observed reflections. The Mn atom is co-ordinated by two Cl anions and four N of two phenanthroline (phen) molecules, forming a distorted octahedron. Two Mn--Cl bond lengths are 2. 437(2) and 2. 449(2) A,respectively. The Mn--N bond lengths vary from 2. 290(3) to 2. 367 (4) A。 The dihedral angle between two phen best planes is 90. 4°.
基金This work was supported by the National Natural Science Foundation of China (No. 20171012) and the Natural Science Foundation of Fujian province (No. E0110010)
文摘The title complex NiL(py)3, where H2L = N-salicylaldehyde-N-phenoxyacetyl hydrazine, was prepared and characterized by X-ray diffraction. The single crystal of the title compound, Ni(C15H12N2O3)(C5H5N)3, is of monoclinic, space group P21/c with a = 11.900(1), b = 9.6855(7), c = 23.658(2) , b = 92.357(2)? V = 2724.5(4) 3, Z = 4, F(000) = 1176, Dc = 1.376 g/cm3, ?= 0.753 mm-1, R = 0.0332 and wR = 0.0820. The coordination polyhedron around the nickel atom is an elongated octahedron. The basal plane consists of one phenol oxygen, one amine carbonyl oxygen and one hydrazine nitrogen atoms from the ligand L2- and one nitrogen atom from one coordinated pyridine ligand, while the axial sites are occupied by two nitrogen atoms of two coordinated pyridine ligands.
基金This research was financially supported by the grants from the State Key Laboratory of Structural Chemistry the National Science and Technology of China (001CB1089)+1 种基金 the Chinese Academy of Sciences (CAS) the National Science Foundation of China (20
文摘Two mononuclear tin(IV) complexes, [Sn(pda)2(edt)2] (pda = o-phenylenediamine) (C16H24N4S4Sn, Mr = 519.32) 1 and [Sn(eda)(edt)2] (eda = ethylenediamine) (C6H16N2S4Sn, Mr = 363.14) 2 were synthesized and characterized by X-ray structure analysis. 1 belongs to trigonal, space group P-3c1 with a = b = 20.0280(6), c = 8.7679(5) ? V = 3045.8(2) ?, Z = 6, Dc = 1.699 g/cm3, m = 1.677 mm-1, F(000) = 1572, the final R = 0.0418 and wR = 0.1019 for 1805 independent reflections. 2 crystallizes in monoclinic, space group P21/c with a = 10.911(3), b = 9.783(2), c = 11.831(3) ? b = 100.28(2), V = 1242.6(6) ?, Z = 4, Dc = 1.941 g/cm3, m = 2.690 mm-1, F(000) = 720, the final R = 0.0280 and wR = 0.0627 for 2166 independent reflections. Both Sn4+ ions in these two complexes are six-coordinated with a slightly distorted octahedral configu- ration.
基金This work was supported by the National Natural Science Foundation of China (50272066) and Key Project of Science and Technology of Fujian Province (2001F004)
文摘The spectral parameters of Nd3+ ions in Nd3+:Klu(WO4)2 crystal were calculated based on Judd-Ofelt theory and obtained as follows: for the oscillator strengths ?λ: ?2 = 7.5029×10-20 cm2, ?4 = 7.1837×10-20 cm2 and ?6 = 3.1189×10-20 cm2; the radiative lifetime is 123 μs; the quantum efficiency is equal to 64.55%; and β1 = 0.5498, β2 = 0.3943, β3 = 0.0551 and β4 = 0.0027 for the fluorescence branch ratios.
基金Financially support by NNSFC (No. 20031020) NSF of Fujian Province and the Key Project from CAS
文摘The hydro(solvo)thermal reactions of cobalt powder or its chloride with 2,5- pyridine dicarboxylic acid (H2PYDC) yielded two new complexes: [Co(II)2(PYDC)2(H2O)2- (H2O)4]n 1 and {Co(II)[NH2(CH3)2]2(PYDC)2}n 2. It is observed that the reactive solvents result in different connectivity modes of ligand and diverse dimensional extension of crystal structures. The correlation between structure and magnetic property will be discussed in this paper. Crystal data for 1: space group P1, a = 7.0419(17), b = 8.937(2), c = 9.6182(19) ?, α = 91.532(4), β = 99.869(10), γ = 107.889(11)o, V = 565.5(2) ?3, Z = 1, Dc = 1.845 g/cm3, μ = 1.56 mm-1, F(000) = 322 , R = 0.0505 and wR = 0.1580; and those for 2: space group C2/c, a = 14.9075(6), b = 8.2523(3), c = 16.9643(2) ?, β = 100.982(2)o, V = 2048.75(11) ?3, Z = 4, Dc = 1.560 g/cm3, μ = 0.892 mm-1, F(000) = 996, R = 0.0443 and wR = 0.1134.
基金This work was supported by the State Key Basic Research and Development Plan (G1998010100) and NNSFC (No. 30170229 29973047 and 39970177)
文摘The crystal structure of the title compound {[Mn(phen)2(OAc)(H2O)]ClO4}2H2O (phen = 1,10-phenanthroline) has been synthesized and determined by X-ray diffraction. The crystal is of triclinic, space group P?with a = 12.7955(4), b = 15.0544(4), c = 16.2183(4) , ?= 64.479(1), b =67.526(1), g = 83.582(1), C52H40Cl2Mn2N8O15, Mr = 1197.70, V = 2600.1(1) ?, Dc = 1.530 g/cm3, F(000) = 1224, = 0.666 cm-1 and Z = 2. The final refinement gave R = 0.0691 and wR = 0.1821 for 6131 observed reflections with I > 2s(I). The cell of the complex contains two uniform mono-manganese molecules [Mn(phen)2(OAc)(H2O)]ClO4 and a solvate water molecule. Four nitrogen atoms from two chelating phenanthroline ligands and one oxygen atom from acetate ligate to the MnⅡ ion, forming a distorted octahedral geometry together with one coordinated water molecule. One ClO4- anion and one water molecule exist outside the cation [Mn(phen)2(OAc)- (H2O)]+ as a counter ion and solvate molecule, respectively.
文摘[Mo3S4(μ-CH3COO)[S2P(OEt)2]3(py)]·(CH3COOCH2CH3) , Mr = 1197. 96,monoclinic,P21/n,a=13. 158(2),b=23. 153(5), c=16. 175(3) A,β = 112. 79(1)°,V=4543. 1(7)A3,Z=4, Dc= 1. 751g/cm-3,λ(MoKa) = 0. 71073A ,μ= 13. 799cm-1,F(000) = 2408. Final R=0. 067 for 4000 reflections. The structure consists of the neutral cluster molecule [Mo3S4(μ-OAc) (dtp)3(py)] (dtp = [S2P(OEt)2]) and the solvent ethyl acetate (AcOEt). The three Mo-Mo bond lengths in the title compound are 2. 691(2) ,2. 747(2) ,2. 762(2) A ,whereas the Mo-N bond length in Mo(3) position is 2. 36(2)A. The important bond lengths of these Mo clusters with (py) ring at the loose coordination site are listed for comparison.
基金This work was supported by the foundation of Natural Science Research of Jiangsu Education Department (02KJB150007)
文摘The title complex [Cu3L3(H2O)]DMFH2O (H2L = 4-(3-hydroxy-2-ethyl-4- pyridinone-1-yl)-aniline condensation salicylaldehyde) was obtained. The single-crystal X-ray study shows that it is a trinuclear compound [Cu3(C20H15N2O3)3(H2O)]DMFH2O. The coordi- nation sphere about each copper ion in the complex consists of two oxygen atoms from hydroxylpyridinone moiety of one ligand and one oxygen and one nitrogen atoms from salicyladehyde Schiff-base moiety of another ligand arranged in a slightly distorted square planar geometry. Among the three copper ions, one (Cu(2)) is coordinated by the other oxygen atom of water molecule on the fifth coordinate position to form a distorted square pyramid geometry. The crystal is of monoclinic, space group P21/c with a = 12.9202(5), b = 27.197(1), c = 17.0116(7) ? b = 100.588(1), V = 5875.9(4) 3, Z = 4, C63H57N7O12Cu3, Mr = 1294.78, Dc = 1.464 g/cm3, m = 1.146 mm-1, F(000) = 2668, R = 0.0784 and wR = 0.1546 for 6926 observed reflections with I > 2s(I). The differences of coordinate bond lengths are observed between anhydrous and hydrous units: in the former unit, the average bond lengths are 1.978 ?for CuN (azomethine), 1.883 ?for CuO (phenolic) in Schiff-base moiety, 1.959 ?for CuO (keto), and 1.919 ?for CuO (hydroxy) in hydroxypyridinone moiety; while those in the latter are longer with the following corresponding values: 1.985(5), 1.908(5), 1.993(5) and 1.919(4) ? respectively. The Cu(2)O (water) bond length is 2.375(6) ?
文摘A two-dimensional hydrogen-bonded cadmium(II) compound [Cd(dapm)2- (CH3COO)2(H2O)2] (dapm = diaminodiphenylmethane) has been synthesized and characterized by single-crystal X-ray diffraction analysis. It crystallizes in monoclinic, space group C2/c with a = 27.572(3), b = 5.5064(5), c = 23.310(2) , = 124.785(1)o, C15H19Cdo.5ON2O3, Mr =331.52, V = 2906.6(5) ?, Z = 4, Dc = 1.515 g/cm3, F(000) = 1368 and = 0.801 mm-1. The final R = 0.0403 and wR = 0.1014 for 1795 observed reflections with I≥4(I). The centrosymmetric Cd(II) is six- coordinated in a distorted octahedral geometry, and the dapm in a trans mode acts as a monoden- tate ligand. The intermolecular hydrogen bonds among coordinated aqua molecules with coordi- nated acetate oxygen atoms and uncoordinated dapm nitrogen atoms form a two-dimensional supramolecular framework.
基金This work was supported by the NNSF of China (Nos. 20271050 and 20473093), the Talents Program of the Chinese Academy of Sciences and NSF of Fujian Province (Nos. E0510030 and E0210029)
文摘The crystal structures of two coordination polymers [Ln(IN)3(H2O)2]n (Ln = Nd 1, Gd 2; IN = isonicotinate) were determined by single-crystal X-ray diffraction and further chara- cterized by IR, elemental analysis and thermogravimetric analysis. Crystal data for 1: monoclinic, space group P21/c, a = 9.6636(5), b = 19.7532(10), c = 11.6183(6) ?, β = 112.032(1)°, V = 2055.83(18) ?3, Z = 4, Dc = 1.766 g/cm3, F(000) = 1076, μ = 2.575 mm–1 and R = 0.0493; Crystal data for 2: monoclinic, space group C2/c, a = 20.251(2), b = 11.6199(11), c = 9.8240(9) ?, β = 115.505(3)°, V = 2086.4(3) ?3, Z = 4, Dc = 1.781 g/cm3, F(000) = 1092, μ = 3.228 mm–1 and R = 0.0695. In the title compounds, the center atoms Ln(III) are in a distorted square antiprismatic geometry and linked by bridging isonicotinate to form an infinite chain. The intermolecular hydro- gen bonds lead to the formation of three-dimensional supramolecular structures.
基金This work was supported by the National Natural Science Foundation of China (20073048) NSF of Fujian and the Chinese Academy of Sciences
文摘A hydrothermal reaction of copper acetate with ammonium molybdate, 4,4-bpy (4,4-bipyridine) and 1,10-phen (1,10-phenanthroline) led to the formation of brown crystals of [Cu2(1,10-phen)2(4,4-bpy)]2 [Mo8O26]4H2O 1. Single-crystal X-ray analysis has revealed that 1 (C68H56N12O30Cu4Mo8) crystallizes in the triclinic system, space group P with a = 11.270(3), b = 13.113(6), c = 13.906(3) ? = 103.33(4), b = 98.54(2), g = 101.29(2)? V = 1920.1(1) ?3, Mr = 2542.93, Z = 1, Dc = 2.199 g/cm3, m = 2.435 mm-1, F(000) = 1240, the final R = 0.0445, wR = 0.1082 and S = 1.021 for 5052 observed reflections with I >2s(I). It consists of copper (Ⅰ) tetramer units and -[Mo8O26]4- anions, which are further attached into a three-dimensional framework through hydrogen bonding and - stacking interactions.
文摘A novel supramolecular adduct 3(C 42H 42N 28O 14) 2·H 2O (1) was synthesized by mixing 2- and cucurbit uril in solution of hydrochloric acid. The crystal structure was determined by single crystal X-ray diffraction analysis. The crystal belongs to orthorhombic system and space group F dd2 with cell dimensions: a=4.705 33 (5) nm, b=7.153 80 (6) nm, c= 1.894 61 (2) nm, Z=16, V=63.7744 (11) nm3, D c= 1.534 g/cm3, μ=3.007 mm -1, F(000)=29 120, R 1= 0.070 7, wR 2=0.169 2. In crystal, the cucurb uril molecules form two zig-zag chains.
基金The project was supported by the Key Project of Science and Technology of Fujian province (2001H107) and the National Natural Science Foundation of China (N0. 50272066)
文摘Crystals of the low temperature phase b-Ba3Y(BO3)3 have been synthesized by the flux method. The structure of the title compound crystallizes in the hexagonal system, space group P63cm with the following parameters: a = 9.416(3), c = 17.536(8) ? V = 1346.6(8) ?, Ba3YB3O9, Mr = 677.36, Z = 6, Dc = 5.012 g/cm3, l(MoKa) = 0.71073 ? m = 19.409 mm-1, Flack parameter = 0.02(3), F(000) = 1764, R = 0.0714 and wR = 0.1696 for 1076 observed reflections with I > 2s(I). The compound contains two sets of YO6 octahedra, four sets of BaO9 polyhedra and three sets of BO3 planar triangles.
