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1.
Shuxiang Wang Yanan Shi Wenqing Shao Jianlong Du Haiying Wei Jinchao Zhang Ke Wang Shigang Shen Shenghui Li Jitai Li Yangyang Zhao 《应用有机金属化学》2012,26(10):504-510
Six new gold(III) complexes [Au(bzpam)Cl2] (1, bzpamH = N‐benzyl picolinamide), [Au(hetpam)Cl2] (2, hetpamH = N‐(2‐hydroxyethyl) picolinamide), [Au(pypam)Cl]AuCl4 (3, pypamH = N‐(pyridin‐2‐ylmethyl) picolinamide), [Au(dmepam)Cl]AuCl4 (4, dmepamH = N‐(2‐(dimethylamino)ethyl) picolinamide), [Au(bhetpydam)Cl] (5, bhetpydamH2 = N,N′‐bis(2‐hydroxyethyl) pyridine‐ 2,6‐dicarboxamide) and [Au2(hedam)Cl4] (6, hedamH2 = N,N′‐(hexane‐1,6‐diyl) dipicolinamide) with deprotonated pyridyl carboxamide were synthesized and characterized by elemental analysis, molar conductivity, IR, H1 NMR and C13 NMR techniques. The analytical data showed that deprotonated pyridyl carboxamide coordinated with gold(III) ions through a nitrogen atom. The cytotoxicity against Bel‐7402 and HL‐60 cell lines was tested by MTT (3‐(4,5‐Dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide) and SRB (sulforhodamine B) assays. The results indicated that the complexes exerted cytotoxic effects against Bel‐7402 and HL‐60 cell lines, complex 6 had better cytotoxicity than cisplatin, and complex 3 displayed similar cytotoxicity to cisplatin against Bel‐7402 cell line. The results suggested that the characteristics of ligands had an important effect on cytotoxicity of complexes. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
2.
Murat Çelik Cemalettin Alp M. Serdar Gültekin Metin Balci 《Tetrahedron letters》2006,47(22):3659-3663
1,2- and 1,3-Bis(trifluoroacetoxy) alcohols are easily obtained from the one-pot reaction of alkenes with phenyliodine(III) bis(trifluoroacetate) (PIFA) in the absence of any additive or catalyst. The products were converted into the corresponding diols by ammonolysis. The use of bicyclic alkenes has shown that rearranged 1,3-diacetoxy alcohols are mostly formed as the major products. 相似文献
3.
Complexes of Co(III) with 2-hydroxyacetophenone-thiosemicarbazone, 2-hydroxy-3-methylacetophenonethiosemicarbazone and 2-hydroxy-4-methyl-acetophenonethiosemicarbazone,
and the addition complexes of 2-hydroxy-acetophenone thiosemicarbazone with ammonia, pyridine, aniline,o-toluidine,m-toluidine andp-toluidine have been synthesized and characterized on the basis of their conductivities, electronic and infrared spectral
data. All complexes are low-spin octahedral in nature. Various parameters have been obtained using ligand field theory. 相似文献
4.
《Journal of Coordination Chemistry》2012,65(19):3187-3197
New Sm(III) and Gd(III) complexes of deprotonated 4-hydroxy-3[1-(4-nitrophenyl)-3-oxobutyl]-2H-1-benzopyran-2-one (Acenocoumarol) were synthesized and characterized using FT-IR, FT-Raman, NMR spectra, and elemental analyses. The vibrational study gave evidence for the coordination of ligand to lanthanide ions. The ligand and its lanthanide(III) complexes were tested for their cytotoxic/cytostatic activity against two tumor cell lines and peritoneal mouse macrophages. The Sm(III) and Gd(III) complexes exhibit good activity against melanoma B16 and fibrosarcoma L929 and are stronger inhibitors of tumor cell proliferation than the ligand. Besides their cytotoxicity to tumor cells, Acenocoumarol and its gadolinium(III) and samarium(III) complexes modulate NO generation in activated macrophages. 相似文献
5.
Daniel De Moraes Profirio Raphael Enoque Ferraz De Paiva Camilla Abbehausen Alexandre Cuin Norberto Masciocchi Daisy Machado 《Journal of Coordination Chemistry》2016,69(18):2707-2722
A gold(III) complex with N,N′-ethylenebis(pyrrol-2-yl-methyleneamine) (H2pyren) was synthesized and characterized by physicochemical and spectroscopic measurements. Density functional theory (DFT) studies and cytotoxic assays were performed. Infrared, mass spectrometry, and 1H, 13C, and {15N,1H} nuclear magnetic resonance analyses indicate that pyren is deprotonated and gold(III) is four coordinate in a square planar environment, with the pyrrole and imine nitrogens as donors. The structure was confirmed by powder X-ray diffraction and confirmed as a minimum of the potential energy surface by DFT. Cytotoxic activity of [Au(pyren)]+ was active against three tumorigenic cell lines with IC50 values of 35 μM. Interaction studies with CT-DNA by fluorescence and competition with ethidium bromide (EB) showed a quenching of the emission band of DNA with a Stern–Volmer quenching constant value of (3.0 ± 0.1) × 104 M?1 and a decrease in fluorescence quenching of EB-DNA system, respectively, confirming that DNA is a possible target for the complex via an intercalative binding, which was confirmed by DNA conformational changes observed with circular dichroism spectroscopy. 相似文献
6.
Qurratul Ain Sarvesh Kumar Pandey Om Prakash Pandey Soumitra Kumar Sengupta 《应用有机金属化学》2016,30(2):102-108
A series of neodymium(III) and samarium(III) complexes of type [Ln(L)Cl(H2O)3] have been synthesized with Schiff bases (LH2) derived from 3‐(phenyl/substituted phenyl)‐4‐amino‐5‐mercapto‐1,2,4‐triazoles and isatin. The structures of the complexes were established using elemental analysis, molar conductivities, magnetic moments, infrared, NMR (1H, 13C) and UV–visible spectra, X‐ray diffraction and mass spectrometry. The thermal behaviour of these compounds under non‐isothermal conditions was investigated using thermogravimetry and differential thermogravimetry. The intermediates obtained at the end of various thermal decomposition steps were identified from elemental analysis and infrared spectral studies. All the ligands and their complexes were also screened for their antibacterial activity against Staphylococcus aureus and Bacillus subtilis and antifungal activity against Aspergillus niger, Aspergillus flavus and Colletotrichum capsici. The screening results were correlated with the structural features of the compounds. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
7.
《Journal of Coordination Chemistry》2012,65(10):1677-1689
Reaction of 2-hydroxy-1-naphthaldehydebenzoylhydrazone(napbhH2) with manganese(II) acetate tetrahydrate and manganese(III) acetate dihydrate in methanol followed by addition of methanolic KOH in molar ratio (2 : 1 : 10) results in [Mn(IV)(napbh)2] and [Mn(III)(napbh)(OH)(H2O)], respectively. Activated ruthenium(III) chloride reacts with napbhH2 in methanolic medium yielding [Ru(III)(napbhH)Cl(H2O)]Cl. Replacement of aquo ligand by heterocyclic nitrogen donor in this complex has been observed when the reaction is carried out in presence of pyridine(py), 3-picoline(3-pic) or 4-picoline(4-pic). The molar conductance values in DMF (N,N-dimethyl formamide) of these complexes suggest non-electrolytic and 1 : 1 electrolytic nature for manganese and ruthenium complexes, respectively. Magnetic moment values of manganese complexes suggest Mn(III) and Mn(IV), however, ruthenium complexes are paramagnetic with one unpaired electron suggesting Ru(III). Electronic spectral studies suggest six coordinate metal ions in these complexes. IR spectra reveal that napbhH2 coordinates in enol-form and keto-form to manganese and ruthenium metal ions in its complexes, respectively. ESR studies of the complexes are also reported. 相似文献
8.
9.
Man-Kit Lau Qian-Feng Zhang Wing-Tak Wong Wa-Hung Leung 《Journal of organometallic chemistry》2004,689(14):2401-2410
Treatment of [M(Buppy)2Cl]2 (M=Ir (1), Rh (2); BuppyH=2-(4′-tert-butylphenyl)pyridine) with Na(Et2NCS2), K[S2P(OMe)2], and K[N(Ph2PS)2]2 afforded monomeric [Ir(Buppy)2(S∧S)] (S∧S=Et2NCS2 (3), S2P(OMe)2 (4), N(PPh2S)2 (5)) and [Rh(Buppy)2(S∧S)] (S∧S=Et2NCS2 (6), S2P(OMe)2 (7), N(PPh2S)2 (8)), respectively. Reaction of 1 with Na[N(PPh2Se)2] gave [Ir(Buppy)2{N(PPh2Se)2}] (9). The crystal structures of 3, 4, 7, and 8 have been determined. Treatment of 1 or 2 with AgOTf (OTf=triflate) followed by reaction with KSCN gave dinuclear [{M(Buppy)2}2(μ-SCN)2] (M=Ir (10), Rh (11)), in which the SCN− ligands bind to the two metal centers in a μ-S,N fashion. Interaction of 1 and 2 with [Et4N]2[WQ4] gave trinuclear heterometallic complexes [{Ir(Buppy)2}2(μ-WQ4)] (Q=S (12), Se (13)) and [{Rh(Buppy)2}2{(μ-WQ)4}] (Q=S (14), Se (15)), respectively. Hydrolysis of 12 led to formation of [{Ir(Buppy)2}2{W(O)(μ-S)2(μ3-S)}] (16) that has been characterized by X-ray diffraction. 相似文献
10.
11.
Two procedures are proposed for the potentiometric determination of Ag(I), Pd(II) and Au(III) in binary mixtures, by titration with potassium iodide solution, and use of a commercial iodide electrode as sensor. In the first procedure, two aliquots of the mixture are titrated, at pH 2.0 ± 0.2 and 9.0 ± 0.2, adjusted with dilute sulphuric acid and ammonia solution. At pH 2.0, the titrant reacts with both metals, whereas at pH 9.0, Ag(I) is the only reactant. The second procedure utilizes titration of two aliquots of the mixture in the presence and absence of a selective masking agent. The methods have been applied to the determination of these metals in some jewellery alloys. 相似文献
12.
Will E. Lynch Clifford W. Padgett Brandon Quillian John Haddock 《Acta Crystallographica. Section C, Structural Chemistry》2015,71(4):298-300
The cationic pseudo‐square‐planar complex tetrakis(1‐methyl‐2,3‐dihydro‐1H‐imidazole‐2‐thione‐κS)gold(III) trichloride sesquihydrate, [Au(C4H6N2S)4]Cl3·1.5H2O, was isolated as dark‐red crystals from the reaction of chloroauric acid trihydrate (HAuCl4·3H2O) with four equivalents of methimazole in methanol. The AuIII atoms reside at the corners of the unit cell on an inversion center and are bound by the S atoms of four methimazole ligands in a planar arrangement, with S—Au—S bond angles of approximately 90°. 相似文献
13.
The reaction of LLi, (L = [RNC(Me)CHC(Me) = O] (R = C2H4NEt2)), with AlCl3 at −78 °C forms the mono-ketiminate product, LAlCl2, 1, while the same reaction at 0 °C affords the bis-ketiminate complex, [{(LH)2AlCl}(Cl2)], 2, Reduction of 1 with Lio, Ko or Mgo yielded an unusual dimeric aluminum(III) species, [L′AlCl]2, 3, where C-C coupling of the ligand backbone is observed. 相似文献
14.
Synthesis and characterization of Pr(III), Nd(III) and Er(III) complexes with 2,6-pyridinedimethanol
The reactions of Ln(NO3)3?6H2O (Ln=Pr, Nd or Er) with the potentially tridentate O,N,O chelating ligand 2,6-pyridinedimethanol (H2pydm) in a 1:2 M ratio were investigated, and complexes with the formula [Ln(H2pydm)2(NO3)2](NO3) (Ln=Pr or Nd) (1 and 2) and [Er(H2pydm)3](NO3)3 (3) were isolated. The compounds contain 10-coordinate Pr(III) and Nd(III) ions that crystallize in the triclinic space group P-1 while the 9-coordinate Er(III) complex crystallizes in the monoclinic system (P21/n). A new lanthanide complex, [Pr(H2pydm)3](Cl)3?DMF (4), has been synthesized by reaction of PrCl3?6H2O and H2pydm. The nine-coordinate Pr(III) is bound to three H2pydm ligands. X-ray crystal structures of 1–4 reveal that the ligand coordinates tridentate via the pyridyl nitrogen and the two hydroxyl oxygens. The electronic absorption spectra of 1–4 show 4f–4f transitions. 相似文献
15.
Heteroleptic half-sandwich Ru(II), Rh(III) and Ir(III) complexes based on 5-ferrocenyldipyrromethene
Mahendra Yadav 《Journal of organometallic chemistry》2011,696(3):758-763
The synthesis and characterization of heteroleptic complexes with the formulations [(η6-arene)RuCl(fcdpm)] (η6-arene = C6H6, C10H14) and [(η5-C5Me5)MCl(fcdpm)] (M = Rh, Ir; fcdpm = 5-ferrocenyldipyrromethene) have been reported. All the complexes have been characterized by elemental analyses, IR, 1H NMR and electronic spectral studies. Structures of [(η6-C6H6)RuCl(fcdpm)] and [(η6-C10H14)RuCl(fcdpm)] have been determined crystallographically. Chelating monoanionic linkage of fcdpm to the respective metal centres has been supported by spectral and structural studies. Further, reactivity of the representative complex [(η6-C10H14)RuCl(fcdpm)] with ammonium thiocyanate (NH4SCN) and triphenylphosphine (PPh3) have been examined. 相似文献
16.
Complexes of the general formula [ReIII(L)Cl(PPh3)2] have been synthesised by reacting H2L and [ReOCl3(PPh3)2] in ethanol. Here H2L represents imines of α-amino acids (glycine, l-alanine, l-valine, l-phenylalanine) derived from salicylaldehyde and naphthaldehyde. The crystal structure of one complex has been determined. The complexes are mononuclear, paramagnetic and display paramagnetic 1H NMR in CDCl3 solution. Their spectral and redox properties are scrutinised. 相似文献
17.
Spectroscopic Characterization and Crystal Structure of Trifluoromethyl Iodine(III) Chloride Trifluororacetate (CF3I(Cl)OCOCF3) The ternary iodine(III) compound CF3I(Cl)OCOCF3 is obtained by reaction between CF3I(Cl)F and (CH3)3SiOCOCF3 at –50 °C. The molecule was characterized by vibrational spectra, NMR‐spectra, and a crystal structure analysis. CF3I(Cl)OCOCF3 crystallizes monoclinic in the space group P21/c with a = 1102.7(1) pm, b = 785.6(1) pm, c = 989.7(1) pm, and β = 101.34(1)°. 相似文献
18.
《Journal of Coordination Chemistry》2012,65(4):371-378
The vanadium(III) complexes, V(S2CNMe2)3 (1) and V(S2CN i Pr2)3 (2) were prepared and characterized by analysis, IR, electronic and 1H NMR spectra. The complexes show reversible thermochromic behaviour. MM2 calculations were used to simulate the molecular structure of 1. For 2, variable temperature 1H NMR revealed hindered rotation about C–N bonds. The rotational energy barrier (38?kJ?mol?1) was obtained by molecular mechanics force-field calculations. 相似文献
19.
Four new complexes of Au(III), Pd(II), Ni(II), and Cu(II) ions were synthesized, derived from a novel heterocyclic ligand (L) that has both triazole and tetrazole rings. The ligand synthesis was through successive steps to achieve both heterocyclic rings. The synthesized compounds were characterized using conventional techniques like infrared, ultra violet—visible and proton/carbon nuclear magnetic resonance spectroscopy, metal and thermal analyses, and molar conductivity. All complexes were suggested to have square planar geometry, gold, nickel, and palladium complexes were salts while copper neutral complexes have the chemical formulas; [AuL2]Cl.2H2O, [PdL2]Cl2.2H2O, [NiL2]Cl2.2H2O, and [CuL2]. The cytotoxic effect was studied on breast cancer cell line (MCF‐7 cell line) at different concentrations by using the 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide assay method, for the ligand (L) and complexes. The results showed that gold(III) and nickel(II) complexes have the highest cytotoxicity among all compounds against cancer cell lines. 相似文献
20.
Santanu Mandal Tinku Sen Uttam Mandal Dipankar Bhunia Corrado Rizzoli 《Journal of Coordination Chemistry》2019,72(22-24):3614-3624
AbstractFour new mononuclear Schiff base manganese(III) and cobalt(III) complexes viz. [Mn(L1)(NCS)] (1), [Mn(L2)(NCS)] (2), [Co(L3)(NCS)] (3), and [Co(L4)(NCS)]·0.5CH3OH·0.5H2O (4), containing thiocyanate as a common pseudohalide ion are reported. The pentadentate Schiff base ligands H2L1, H2L2, H2L3, and H2L4 were obtained by the condensation of substituted salicylaldehydes with N-(3-aminopropyl)-N-methylpropane-1,3-diamine. The syntheses of the complexes have been achieved by the reaction of manganese(II) perchlorate or cobalt(II) perchlorate with the respective Schiff bases in the presence of thiocyanate in methanol medium. Complexes 1–4 have been characterized by microanalytical, spectroscopic, single-crystal X-ray diffraction and other physicochemical studies. Structural studies reveal that 1–4 adopt nearly similar structures containing the MN4O2 (M?=?Mn, Co) chromophore in which each central M(III) ion adopts a distorted octahedral geometry. Weak intermolecular H-bonding interactions are operative in these complexes to bind the molecular units. The antibacterial activity of 1–4 and their constituent Schiff bases has been tested against some common bacteria. 相似文献