A novel anionic organotin(Ⅳ) complex {[(pClCHCH)Sn(HO)(Cl)OCOCH(O)CH(O)COSn(HO)(Cl)(p-ClCHCH)]·2(HNEt)}(1) was synthesized by the reaction of di(p-chlorobenzy)tin dichloride with the D-tartaric acid in 2:1 molar...A novel anionic organotin(Ⅳ) complex {[(pClCHCH)Sn(HO)(Cl)OCOCH(O)CH(O)COSn(HO)(Cl)(p-ClCHCH)]·2(HNEt)}(1) was synthesized by the reaction of di(p-chlorobenzy)tin dichloride with the D-tartaric acid in 2:1 molar in the presence of an organic base triethylamine. The structure was characterized by elemental analysis, IR, TG, XRD and single-crystal X-ray diffraction. It crystallizes in triclinic, P1 space group, with a = 0.7067(1), b = 1.9762(3), c = 2.2383(3) nm, α = 91.544(2)°, β = 90.075(2)°, γ = 90.110(2)°, V = 3.1247(7) nm~3, Z = 3, Dc = 1.621 g/cm~3, m(Mo Kα) = 16.29 cm–1, F(000) = 1530, R = 0.0394, wR = 0.1092,(Δρ)max = 1224 and(Δρ)min = –840 e/nm~3. The stabilities, orbital energies and composition characteristics of some frontier molecular orbitals of 1 have been carefully investigated with quantum chemistry calculation. In addition, the in vitro antitumor activity suggested that 1 had stronger inhibitory activity on H460, MCF7 than on A549.展开更多
Four new five-coordinated anionic tin(Ⅳ) complexes with a form of [R_ n NH_ 4- n ][PhSn( μ 2-SCH_2COO)_2] were synthesized via the reaction of mercaptoacetic acid with phenyltin trichloride in the presence of dif...Four new five-coordinated anionic tin(Ⅳ) complexes with a form of [R_ n NH_ 4- n ][PhSn( μ 2-SCH_2COO)_2] were synthesized via the reaction of mercaptoacetic acid with phenyltin trichloride in the presence of different organic bases and characterized by means of IR, 1H NMR and MS spectroscopies. The crystal structure of [( i -Pr)_2NH_2] [PhSn( μ 2-SCH_2COO)_2] was determined by X-ray diffraction. In the crystal structure,the tin atom is five-coordinated and exists in trigonal bipyramid geometry with cell parameters a =1.1766(11) nm, b =1.3144(14) nm, c =1.3336(15) nm,β =90° and Z =4.展开更多
A hydrazone compound 3-chloro-N＇-（3,5-dichloro-2-hydroxybenzylidene）benzo-hydrazide（H2L） derived from the condensation of 3,5-dichlorosalicylaldehyde with 3-chloro-benzohydrazide and its oxovanadium（V） complex ...A hydrazone compound 3-chloro-N＇-（3,5-dichloro-2-hydroxybenzylidene）benzo-hydrazide（H2L） derived from the condensation of 3,5-dichlorosalicylaldehyde with 3-chloro-benzohydrazide and its oxovanadium（V） complex [VOL（CH3OH）（OCH3）] have been successfully prepared and characterized by physico-chemical methods and single-crystal X-ray diffraction.The hydrazone ligand coordinates to the V atom through the phenolate O,imine N,and enolic O atoms.The V atom is hexa-coordinated in a distorted octahedral geometry.The antimicrobial activities（MIC） of the hydrazone ligand and the oxovanadium（V） complex have been evaluated against the bacteria Staphylococcus aureus,Baccilus subtilis,Pseudomonas aeruginosa,and Escherichia coli.展开更多
Three mononuclear oxovanadium complexes [VO(Hbid)(CF3PIP)] (1) (Hbid=(E)-2-(2-hydroxybenzylideneamino) isoindoline-1,3-dione, CF3PIP=2-(2-trifluoromethyl phenyl)imidazole[4,5-f][1,10] phenanthroline), [VO(Hbid)(m-CF3P...Three mononuclear oxovanadium complexes [VO(Hbid)(CF3PIP)] (1) (Hbid=(E)-2-(2-hydroxybenzylideneamino) isoindoline-1,3-dione, CF3PIP=2-(2-trifluoromethyl phenyl)imidazole[4,5-f][1,10] phenanthroline), [VO(Hbid)(m-CF3PIP)];(2) (m-CF3PIP=2-(3-trifluoromethyl phenyl)imidazole [4, 5-f][1,10]phenanthroline) and [VO(Hbid)(p-CF3PIP)];(3) (p-CF3PIP=2-(4-trifluoromethyl phenyl) imidazole[4,5-f][1,10]phenanthroline) have been synthesized and characterized by elemental analysis, IR, molar conductance, ES-MS and 1H NMR. The DNA-binding properties of these complexes were studied by using UV-Vis absorption titration, fluorescence spectra, viscosity measurements and thermal denaturation studies. The results show that 1, 2 and 3 interact with calf thymus DNA (CT-DNA) by intercalation modes and the magnitude of their intrinsic binding constants (Kb values) follows the order: 2 < 1 < 3. Furthermore, their photocleavage properties with pBR322 plasmid DNA were investigated by agarose gel electrophoresis experiments. The DNA cleavage capacity of complex 3 is also stronger than that of 1 and 2.展开更多
It was found that the oxovanadium(V) complex of triethanolamine (TEA) exhibits catalytic activity to the oxidative cleavage of catechols. On the other hand. the vanadyl nitrilotriacetic acid (NTA) complex is inactiv...It was found that the oxovanadium(V) complex of triethanolamine (TEA) exhibits catalytic activity to the oxidative cleavage of catechols. On the other hand. the vanadyl nitrilotriacetic acid (NTA) complex is inactive. but leads to the formation of stable ternary complex. The main products of the catalytic oxidative cleavage of 3.5-di-tert-butylcatechol were separated and characterized. Based on the results. a reaction mechanism was discussed展开更多
New series of oxovanadium (IV) complexes isolated from 2,4,6-tris-(2-pyridyl)-1,3,5-triazine (L<sup>1</sup>) are incorporated and portrayed using spectroscopic (IR, UV-Vis, ESR, mass spectrometric), magnet...New series of oxovanadium (IV) complexes isolated from 2,4,6-tris-(2-pyridyl)-1,3,5-triazine (L<sup>1</sup>) are incorporated and portrayed using spectroscopic (IR, UV-Vis, ESR, mass spectrometric), magnetic moment, thermal and cyclic voltammetry measurements. The results demonstrate that L<sup>1</sup> acts in various styles of chelation with [V<sub>3</sub>O<sub>3</sub>(L<sup>1</sup>)(SO<sub>4</sub>)<sub>3</sub>(EtOH)<sub>1/2</sub>(H<sub>2</sub>O)<sub>3/2</sub>] 1), [VO(L<sup>1</sup>)(2,4-pentadionate)]·Cl·4HCl 2), [V<sub>2</sub>O<sub>2</sub>(L<sup>1</sup>)(SO<sub>4</sub>)<sub>2</sub>(EtOH)<sub>5/2</sub>] 3), [V<sub>2</sub>O<sub>2</sub>(L<sup>1</sup>)(SO<sub>4</sub>)<sub>2</sub>(EtOH)<sub>3/2</sub>(H<sub>2</sub>O)<sub>1/2</sub>] 4), [VO(L<sup>1</sup>)SO<sub>4</sub> (H<sub>2</sub>O)<sub>3/2</sub>]·2.5H<sub>2</sub>O 5) and [V<sub>2</sub>O<sub>2</sub>(L<sup>1</sup>)(SO<sub>4</sub>)<sub>2</sub>(H<sub>2</sub>O)]·H<sub>2</sub>O 6). The values of magnetic moments and spectral studies suggest a square-pyramidal geometry around the V (IV) ion for all complexes. The molar conductance values suggest that the complexes are non-electrolyte, except the [VO(L<sup>1</sup>) (2,4-pentadionate)] Cl·4HCl. Molecular modeling calculates the bond length, bond angle, chemical reactivity, energy components (Kcal/mol) and binding energy (Kcal/mol) for the isolated complexes. The in vitro antibacterial studies of these complexes screened against pathogenic bacteria prove them as growth inhibiting agents. Antitumor activity is carried out in vitro on human mammary gland (breast) MCF-7 and cervical cancer cell-HeLa has shown that [VO(L<sup>1</sup>)SO<sub>4</sub>(H<sub>2</sub>O)<sub>3/2</sub>]·2.5 H<sub>2</sub>O and [VO(L<sup>1</sup>)(2,4-pentadionate)] Cl·4HCl complexes display the highest powerful activity between all of the investigated complexes.展开更多
The violet polycrystalline (NH4)5[(VO)6(CO3)4(OH)9]·10H2O(NVCO) was simply sy nthesized by solution reaction using V2O5, HCl, N2H4·2HCl and NH4HCO3 as the st arting materials. The results of TGA and DTA of N...The violet polycrystalline (NH4)5[(VO)6(CO3)4(OH)9]·10H2O(NVCO) was simply sy nthesized by solution reaction using V2O5, HCl, N2H4·2HCl and NH4HCO3 as the st arting materials. The results of TGA and DTA of NVCO under H2(99.999%) atmosphe re show that V2O3 forms at 620℃. The data of TG/DTG and DTA of NVCO under N2(99 .999%) atmosphere indicate that VO2 forms at 367℃and crystallizes at 390℃. In air atmosphere, the TG/DTG and DTA of NVCO show that V2O5 forms at 354℃, cryst allizes at 366℃and melts at 664℃. The three thermolysis processes of NVCO show that a large amount of H2O, CO2 and NH3 gases fast releases during the thermoly sis of NVCO, causing that the particles of the materials split and atomize stron gly, thus to obtain V2O3, VO2 and V2O5 nano-powders finally. According to the a bove of thermoanalytical results, V2O3, VO2 and V2O5 powders were prepared respe ctively under H2, N2 and oxygen in a tube furnace. Chemical analysis and XRD exp eriments of the powders identify that pure V2O3 is obtained at 800℃for 0.5h und er H2 atmosphere; crystalline VO2 is obtained at 480℃for 0.5h in N2; amorphous VO2 is obtained at 350℃for 20min under N2 atmosphere, this has been first repor ted to prepare amorphous VO2 powder so far; pure V2O5 is obtained at 400℃for 10 min under oxygen. From the micrographs of the powders, the particle size of the V2O3, the crystalline VO2 or the V2O5 powders is 35nm, 24nm or < 40nm, respectiv ely. Above-mentioned results prove that NVCO is a good precursor for preparatio n of pure V2O3, VO2 and V2O5 nano-powders under mild conditions.展开更多
基金Supported by the Open Fund Project innovation platform of Key Laboratory of Higher Educational Institutions of Hunan Province(GN16K01)Scientific&Technological Projects of Hengyang(2016KL03)+1 种基金Aid programs for Science and Technology Innovative Research Team in Higher Educational Institutions of Hunan Provincethe Key Discipline of Hunan Province,Project funding for research and innovation experiment of university students in Hunan Province
文摘A novel anionic organotin(Ⅳ) complex {[(pClCHCH)Sn(HO)(Cl)OCOCH(O)CH(O)COSn(HO)(Cl)(p-ClCHCH)]·2(HNEt)}(1) was synthesized by the reaction of di(p-chlorobenzy)tin dichloride with the D-tartaric acid in 2:1 molar in the presence of an organic base triethylamine. The structure was characterized by elemental analysis, IR, TG, XRD and single-crystal X-ray diffraction. It crystallizes in triclinic, P1 space group, with a = 0.7067(1), b = 1.9762(3), c = 2.2383(3) nm, α = 91.544(2)°, β = 90.075(2)°, γ = 90.110(2)°, V = 3.1247(7) nm~3, Z = 3, Dc = 1.621 g/cm~3, m(Mo Kα) = 16.29 cm–1, F(000) = 1530, R = 0.0394, wR = 0.1092,(Δρ)max = 1224 and(Δρ)min = –840 e/nm~3. The stabilities, orbital energies and composition characteristics of some frontier molecular orbitals of 1 have been carefully investigated with quantum chemistry calculation. In addition, the in vitro antitumor activity suggested that 1 had stronger inhibitory activity on H460, MCF7 than on A549.
文摘Four new five-coordinated anionic tin(Ⅳ) complexes with a form of [R_ n NH_ 4- n ][PhSn( μ 2-SCH_2COO)_2] were synthesized via the reaction of mercaptoacetic acid with phenyltin trichloride in the presence of different organic bases and characterized by means of IR, 1H NMR and MS spectroscopies. The crystal structure of [( i -Pr)_2NH_2] [PhSn( μ 2-SCH_2COO)_2] was determined by X-ray diffraction. In the crystal structure,the tin atom is five-coordinated and exists in trigonal bipyramid geometry with cell parameters a =1.1766(11) nm, b =1.3144(14) nm, c =1.3336(15) nm,β =90° and Z =4.
基金supported by the Key Program of the Baoji University of Arts and Sciences (No. ZK1018)
文摘A hydrazone compound 3-chloro-N＇-（3,5-dichloro-2-hydroxybenzylidene）benzo-hydrazide（H2L） derived from the condensation of 3,5-dichlorosalicylaldehyde with 3-chloro-benzohydrazide and its oxovanadium（V） complex [VOL（CH3OH）（OCH3）] have been successfully prepared and characterized by physico-chemical methods and single-crystal X-ray diffraction.The hydrazone ligand coordinates to the V atom through the phenolate O,imine N,and enolic O atoms.The V atom is hexa-coordinated in a distorted octahedral geometry.The antimicrobial activities（MIC） of the hydrazone ligand and the oxovanadium（V） complex have been evaluated against the bacteria Staphylococcus aureus,Baccilus subtilis,Pseudomonas aeruginosa,and Escherichia coli.
文摘Three mononuclear oxovanadium complexes [VO(Hbid)(CF3PIP)] (1) (Hbid=(E)-2-(2-hydroxybenzylideneamino) isoindoline-1,3-dione, CF3PIP=2-(2-trifluoromethyl phenyl)imidazole[4,5-f][1,10] phenanthroline), [VO(Hbid)(m-CF3PIP)];(2) (m-CF3PIP=2-(3-trifluoromethyl phenyl)imidazole [4, 5-f][1,10]phenanthroline) and [VO(Hbid)(p-CF3PIP)];(3) (p-CF3PIP=2-(4-trifluoromethyl phenyl) imidazole[4,5-f][1,10]phenanthroline) have been synthesized and characterized by elemental analysis, IR, molar conductance, ES-MS and 1H NMR. The DNA-binding properties of these complexes were studied by using UV-Vis absorption titration, fluorescence spectra, viscosity measurements and thermal denaturation studies. The results show that 1, 2 and 3 interact with calf thymus DNA (CT-DNA) by intercalation modes and the magnitude of their intrinsic binding constants (Kb values) follows the order: 2 < 1 < 3. Furthermore, their photocleavage properties with pBR322 plasmid DNA were investigated by agarose gel electrophoresis experiments. The DNA cleavage capacity of complex 3 is also stronger than that of 1 and 2.
文摘It was found that the oxovanadium(V) complex of triethanolamine (TEA) exhibits catalytic activity to the oxidative cleavage of catechols. On the other hand. the vanadyl nitrilotriacetic acid (NTA) complex is inactive. but leads to the formation of stable ternary complex. The main products of the catalytic oxidative cleavage of 3.5-di-tert-butylcatechol were separated and characterized. Based on the results. a reaction mechanism was discussed
文摘New series of oxovanadium (IV) complexes isolated from 2,4,6-tris-(2-pyridyl)-1,3,5-triazine (L<sup>1</sup>) are incorporated and portrayed using spectroscopic (IR, UV-Vis, ESR, mass spectrometric), magnetic moment, thermal and cyclic voltammetry measurements. The results demonstrate that L<sup>1</sup> acts in various styles of chelation with [V<sub>3</sub>O<sub>3</sub>(L<sup>1</sup>)(SO<sub>4</sub>)<sub>3</sub>(EtOH)<sub>1/2</sub>(H<sub>2</sub>O)<sub>3/2</sub>] 1), [VO(L<sup>1</sup>)(2,4-pentadionate)]·Cl·4HCl 2), [V<sub>2</sub>O<sub>2</sub>(L<sup>1</sup>)(SO<sub>4</sub>)<sub>2</sub>(EtOH)<sub>5/2</sub>] 3), [V<sub>2</sub>O<sub>2</sub>(L<sup>1</sup>)(SO<sub>4</sub>)<sub>2</sub>(EtOH)<sub>3/2</sub>(H<sub>2</sub>O)<sub>1/2</sub>] 4), [VO(L<sup>1</sup>)SO<sub>4</sub> (H<sub>2</sub>O)<sub>3/2</sub>]·2.5H<sub>2</sub>O 5) and [V<sub>2</sub>O<sub>2</sub>(L<sup>1</sup>)(SO<sub>4</sub>)<sub>2</sub>(H<sub>2</sub>O)]·H<sub>2</sub>O 6). The values of magnetic moments and spectral studies suggest a square-pyramidal geometry around the V (IV) ion for all complexes. The molar conductance values suggest that the complexes are non-electrolyte, except the [VO(L<sup>1</sup>) (2,4-pentadionate)] Cl·4HCl. Molecular modeling calculates the bond length, bond angle, chemical reactivity, energy components (Kcal/mol) and binding energy (Kcal/mol) for the isolated complexes. The in vitro antibacterial studies of these complexes screened against pathogenic bacteria prove them as growth inhibiting agents. Antitumor activity is carried out in vitro on human mammary gland (breast) MCF-7 and cervical cancer cell-HeLa has shown that [VO(L<sup>1</sup>)SO<sub>4</sub>(H<sub>2</sub>O)<sub>3/2</sub>]·2.5 H<sub>2</sub>O and [VO(L<sup>1</sup>)(2,4-pentadionate)] Cl·4HCl complexes display the highest powerful activity between all of the investigated complexes.
文摘The violet polycrystalline (NH4)5[(VO)6(CO3)4(OH)9]·10H2O(NVCO) was simply sy nthesized by solution reaction using V2O5, HCl, N2H4·2HCl and NH4HCO3 as the st arting materials. The results of TGA and DTA of NVCO under H2(99.999%) atmosphe re show that V2O3 forms at 620℃. The data of TG/DTG and DTA of NVCO under N2(99 .999%) atmosphere indicate that VO2 forms at 367℃and crystallizes at 390℃. In air atmosphere, the TG/DTG and DTA of NVCO show that V2O5 forms at 354℃, cryst allizes at 366℃and melts at 664℃. The three thermolysis processes of NVCO show that a large amount of H2O, CO2 and NH3 gases fast releases during the thermoly sis of NVCO, causing that the particles of the materials split and atomize stron gly, thus to obtain V2O3, VO2 and V2O5 nano-powders finally. According to the a bove of thermoanalytical results, V2O3, VO2 and V2O5 powders were prepared respe ctively under H2, N2 and oxygen in a tube furnace. Chemical analysis and XRD exp eriments of the powders identify that pure V2O3 is obtained at 800℃for 0.5h und er H2 atmosphere; crystalline VO2 is obtained at 480℃for 0.5h in N2; amorphous VO2 is obtained at 350℃for 20min under N2 atmosphere, this has been first repor ted to prepare amorphous VO2 powder so far; pure V2O5 is obtained at 400℃for 10 min under oxygen. From the micrographs of the powders, the particle size of the V2O3, the crystalline VO2 or the V2O5 powders is 35nm, 24nm or < 40nm, respectiv ely. Above-mentioned results prove that NVCO is a good precursor for preparatio n of pure V2O3, VO2 and V2O5 nano-powders under mild conditions.
