A novel organotin complex of μ-pentaoxygen bridged penta（bis-benzyltin） bissalicylate has been synthesized by the reaction of bis-benzyltin oxide and salicylic acid and its structure has been determined by X-ray di...A novel organotin complex of μ-pentaoxygen bridged penta（bis-benzyltin） bissalicylate has been synthesized by the reaction of bis-benzyltin oxide and salicylic acid and its structure has been determined by X-ray diffraction. The crystal belongs to monoclinic, space group P21/n with a = 1.7206（5）, b = 2.1401（6）, c = 2.1488（6）nm, β= 93.325（5）°, V = 7.899（4） nm^3, Z = 4, Dc = 1.564 g/cm^3,μ（MoKα） = 16.17cm^-1, Mr = 1859.94, F（000） = 3692, R1= 0.0755 and wR2= 0.1557. According to structural analysis, the coordination geometry of tin is a distorted trigonal bipyramid, and the ladder-like structure is shaped by four Sn2O2 planar four-membered rings.展开更多
A di-molybdenum carbonyl compound containing thiolate and dithiocarbamate ligands, [Bu4N][（CO）4Mo（μ-SC6H5）2Mo（C5H10dtc）（CO）2] 1 （CsH10dtc = S2CNC5H10）, has been prepared by reaction of [Mo2（SC6H5）2（CO）8...A di-molybdenum carbonyl compound containing thiolate and dithiocarbamate ligands, [Bu4N][（CO）4Mo（μ-SC6H5）2Mo（C5H10dtc）（CO）2] 1 （CsH10dtc = S2CNC5H10）, has been prepared by reaction of [Mo2（SC6H5）2（CO）8] with C5H10dtcNa and [NBu4]Br in acetone. It crystallizes in monoclinic, space group P21/n with a = 13.162（3）, b = 17.466（2）, c = 20.453（4） A,β= 100.77（1）°, Z = 4, V= 4619（2）A^3, C40H56Mo2N2O6S4, Mr = 980.95, De= 1.389 g/cm^3,μ = 7.66 cm^-1, F（000） = 1988 and R = 0.0746 for 5161 observed reflections with I 〉 2σ（I）. The complex contains a [Mo2S2]^2- planar core in which one Mo atom is chelated by a C5H10dtc ligand, leading to different coordination environments of the two Mo atoms. 95Mo NMR measurement indicates that the two Mo atoms are in different oxidation states.展开更多
Twelve novel dithiocarbamates containing 1,2,3-trizaoles group were prepared via one step starting from organic halides, dithiocarbamic acid prop-2-ynyl ester, and sodium azide, using a very simple catalytic system co...Twelve novel dithiocarbamates containing 1,2,3-trizaoles group were prepared via one step starting from organic halides, dithiocarbamic acid prop-2-ynyl ester, and sodium azide, using a very simple catalytic system composed of copper（I） chloride and water at 70 8C. The structures of the new compounds were characterized and screened for their in vitro anti-tumor. Four of the compounds displayed varying levels of anti-tumor activity against the CDC25 B.展开更多
The title complex [RuH（CO）（PPh3）2（4-ClPhNHCS2）]·C6H14 has been prepared and characterized by X-ray diffraction analysis.It crystallizes in the triclinic system,space group P1 with a = 11.0817（2）,b = 14.3...The title complex [RuH（CO）（PPh3）2（4-ClPhNHCS2）]·C6H14 has been prepared and characterized by X-ray diffraction analysis.It crystallizes in the triclinic system,space group P1 with a = 11.0817（2）,b = 14.3889（2）,c = 15.2136（2） ,α = 71.018（1）,β = 74.911（1）,γ = 85.146（1）°,V = 2214.86（6） 3,Z = 2,Mr = 900.4,Dc = 1.350 g/cm3,Mr = 900.40,μ（MoKα） = 0.616 mm-1,F（000） = 926,S = 1.016,the final R = 0.0478 and wR = 0.0947 for 6828 observed reflections with I 2σ（I） and 505 variables.The molecular structure of 1 consists of one neutral complex [RuH（CO）（PPh3）2（4-ClPhNHCS2）] and one hexane solvent molecule.The geometry around ruthenium is pseudo-octahedral with two trans-binding PPh3 ligands and one chelating bidentate 4-ClPhNHCS2- ligand via two sulfur atoms.The average Ru-S,Ru-P and Ru-H bond lengths are 2.4824（8）,2.3495（8） and 1.71（2）,respectively.The electrochemical properties of 1 have been studied in CH2Cl2 solution by cyclic voltammetry.展开更多
The title compound, [P (CH2Ph) Ph3] [PdWS4(S2CNC4H8)], wassynthesized by ligand replacement reaction of Pd(S2CNC4H8)2 with (NH4)2WS4 in thepresence of [P(CH2Ph)Ph3]Cl in CH2Cl2 and characterized by X-ray diffraction a...The title compound, [P (CH2Ph) Ph3] [PdWS4(S2CNC4H8)], wassynthesized by ligand replacement reaction of Pd(S2CNC4H8)2 with (NH4)2WS4 in thepresence of [P(CH2Ph)Ph3]Cl in CH2Cl2 and characterized by X-ray diffraction analy-ses. Crystallographic data: triclinic, observed reflections with . The crys-tal contains discrete cations and anions. Palladium atom in the anion is coordinated by apyrrolidine-derived dithiocarbamate and a tetrathiotungstate. Both dithiocarbamate andtetrathiotungstate act as bidentate ligands through two sulfur atoms chelating palladiumatom. The Pd-W distance is 2- 847(1).展开更多
Thirteen title compounds Ph 3GeS 2CNR 2(1—13) were synthesized by the reaction of \{corre\|\}sponding triphenylgermanium chloride with dithiocarbamates. Their structures were confirmed by elemen\|tal analysis, IR, 1H...Thirteen title compounds Ph 3GeS 2CNR 2(1—13) were synthesized by the reaction of \{corre\|\}sponding triphenylgermanium chloride with dithiocarbamates. Their structures were confirmed by elemen\|tal analysis, IR, 1H NMR, UV and MS. Some of these compounds showed antitumor activities in vitro.展开更多
基金This work was supported by the Natural Science Foundation (05JJ40015) and Basic Research(03JZY3036) of the Hunan Province ,Key Foundation of Education Committee of HuNan Province(03A009) and Sustentation Fund of HenYang Science& Technology bureau (2004-25, 2005KG01-09)
文摘A novel organotin complex of μ-pentaoxygen bridged penta（bis-benzyltin） bissalicylate has been synthesized by the reaction of bis-benzyltin oxide and salicylic acid and its structure has been determined by X-ray diffraction. The crystal belongs to monoclinic, space group P21/n with a = 1.7206（5）, b = 2.1401（6）, c = 2.1488（6）nm, β= 93.325（5）°, V = 7.899（4） nm^3, Z = 4, Dc = 1.564 g/cm^3,μ（MoKα） = 16.17cm^-1, Mr = 1859.94, F（000） = 3692, R1= 0.0755 and wR2= 0.1557. According to structural analysis, the coordination geometry of tin is a distorted trigonal bipyramid, and the ladder-like structure is shaped by four Sn2O2 planar four-membered rings.
文摘A di-molybdenum carbonyl compound containing thiolate and dithiocarbamate ligands, [Bu4N][（CO）4Mo（μ-SC6H5）2Mo（C5H10dtc）（CO）2] 1 （CsH10dtc = S2CNC5H10）, has been prepared by reaction of [Mo2（SC6H5）2（CO）8] with C5H10dtcNa and [NBu4]Br in acetone. It crystallizes in monoclinic, space group P21/n with a = 13.162（3）, b = 17.466（2）, c = 20.453（4） A,β= 100.77（1）°, Z = 4, V= 4619（2）A^3, C40H56Mo2N2O6S4, Mr = 980.95, De= 1.389 g/cm^3,μ = 7.66 cm^-1, F（000） = 1988 and R = 0.0746 for 5161 observed reflections with I 〉 2σ（I）. The complex contains a [Mo2S2]^2- planar core in which one Mo atom is chelated by a C5H10dtc ligand, leading to different coordination environments of the two Mo atoms. 95Mo NMR measurement indicates that the two Mo atoms are in different oxidation states.
基金the National Centre for Drug Screening,Shanghai,China,for evaluating the inhibitory activity against CDC25Bthe Fundamental Research Funds for the Central Universities,Southwest University for Nationalities(No.12NZYTH03)+1 种基金the Natural Science Foundation of Southwest University for Nationalities(No.381010)the Postgraduate Degree Construction Project of Southwest University for Nationalities(No.2013XWD-S0703)for financial support
文摘Twelve novel dithiocarbamates containing 1,2,3-trizaoles group were prepared via one step starting from organic halides, dithiocarbamic acid prop-2-ynyl ester, and sodium azide, using a very simple catalytic system composed of copper（I） chloride and water at 70 8C. The structures of the new compounds were characterized and screened for their in vitro anti-tumor. Four of the compounds displayed varying levels of anti-tumor activity against the CDC25 B.
基金supported by the National Natural Science Foundation of China (20771003)
文摘The title complex [RuH（CO）（PPh3）2（4-ClPhNHCS2）]·C6H14 has been prepared and characterized by X-ray diffraction analysis.It crystallizes in the triclinic system,space group P1 with a = 11.0817（2）,b = 14.3889（2）,c = 15.2136（2） ,α = 71.018（1）,β = 74.911（1）,γ = 85.146（1）°,V = 2214.86（6） 3,Z = 2,Mr = 900.4,Dc = 1.350 g/cm3,Mr = 900.40,μ（MoKα） = 0.616 mm-1,F（000） = 926,S = 1.016,the final R = 0.0478 and wR = 0.0947 for 6828 observed reflections with I 2σ（I） and 505 variables.The molecular structure of 1 consists of one neutral complex [RuH（CO）（PPh3）2（4-ClPhNHCS2）] and one hexane solvent molecule.The geometry around ruthenium is pseudo-octahedral with two trans-binding PPh3 ligands and one chelating bidentate 4-ClPhNHCS2- ligand via two sulfur atoms.The average Ru-S,Ru-P and Ru-H bond lengths are 2.4824（8）,2.3495（8） and 1.71（2）,respectively.The electrochemical properties of 1 have been studied in CH2Cl2 solution by cyclic voltammetry.
文摘The title compound, [P (CH2Ph) Ph3] [PdWS4(S2CNC4H8)], wassynthesized by ligand replacement reaction of Pd(S2CNC4H8)2 with (NH4)2WS4 in thepresence of [P(CH2Ph)Ph3]Cl in CH2Cl2 and characterized by X-ray diffraction analy-ses. Crystallographic data: triclinic, observed reflections with . The crys-tal contains discrete cations and anions. Palladium atom in the anion is coordinated by apyrrolidine-derived dithiocarbamate and a tetrathiotungstate. Both dithiocarbamate andtetrathiotungstate act as bidentate ligands through two sulfur atoms chelating palladiumatom. The Pd-W distance is 2- 847(1).
文摘Thirteen title compounds Ph 3GeS 2CNR 2(1—13) were synthesized by the reaction of \{corre\|\}sponding triphenylgermanium chloride with dithiocarbamates. Their structures were confirmed by elemen\|tal analysis, IR, 1H NMR, UV and MS. Some of these compounds showed antitumor activities in vitro.
