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11.
The new dipyrido[3,2-a:2′,3′-c]phenazine (dppz) copper(II) complex, [Cu(tpy)(dppz)]2+, where tpy is 2,2′:6′,2″-terpyridine, has been prepared and fully characterized by spectroscopic methods and single-crystal X-ray diffraction. Its DNA binding and in vitro cytotoxicity have been also studied. The molecular structure shows a distorted trigonal bipyramidal CuN5 coordination geometry around the copper atom. The bidentate dppz ligand binds in the equatorial plane, while tpy exhibits axial-equatorial bonding. The interaction of the complex with DNA has been investigated by electronic absorption, competitive fluorescence titration, linear dichroism, voltammetric techniques and a gel electrophoresis mobility shift assay. It is proposed that the binding mode of the complex to DNA is of an intercalation nature with the planar dppz ligands located between the base pairs of double-stranded DNA.An in vitro cytotoxicity study of the complex on human breast adenocarcinoma (MCF7) cell line by an MTT assay indicates that the title complex may have the potency to act as an effective anticancer drug, with an IC50 value of 4.57 μM (3.62-5.77). 相似文献
12.
Mehrnoosh?Kangani Nourallah?HazeriEmail author Malek?Taher?Maghsoodlou Khatereh?Khandan-Barani Maryam?Kheyrollahi Fereshteh?Nezhadshahrokhabadi 《Journal of the Iranian Chemical Society》2015,12(1):47-50
Saccharose was applied as an efficient and homogeneous catalyst for one-pot, four-component synthesis of 1,4-dihydropyrano[2,3-c]pyrazole derivatives from aromatic aldehydes, malononitrile, ethyl acetoacetate and hydrazine monohydrate under thermal solvent-free conditions. This protocol has a considerable number of advantages including mild condition, high yields, operational simplicity, environmentally benign and simple work-up procedures. 相似文献
13.
Hassan Hadadzadeh Ali Reza Rezvani Mahmood Karimi Abdolmaleki Khaled Ghasemi Hadi Esfandiari Marzieh Daryanavard 《Journal of chemical crystallography》2010,40(1):48-57
Abstract
Pyridine-2,6-dicarboxylic acid (dipic) was used for the synthesis of a co-crystal with 1,10-phenanthroline-5,6-dione (phen-dione) and a nickel(II) complex. The co-crystal dipic·phen-dione·4H2O (1) has been synthesized and studied by X-ray crystallography. The structure is stabilized with hydrogen bonds between dipic, H2O and phen-dione. It is surprising that there is no direct hydrogen bonding between phen-dione and dipic and yet the molecules co-crystallize in aqueous solution. A new complex of nickel(II), [Ni(phen)(dipic)(H2O)]·4H2O (2), (where phen = 1,10-phenanthroline) has been synthesized and characterized by elemental and thermogravimetric analyses, FT-IR, UV–Vis and 1H-NMR spectroscopy. The structure of (2) has been studied by X-ray crystallography. The coordination around Ni(II) is a distorted octahedron. The crystal packing shows that the dimensionality of (2) is enlarged to 3D, through hydrogen bonds and π–π interactions. Cyclic voltammetry of (2) shows that the Ni(II/I) couple is irreversible. 相似文献14.
The crystal structure of 1,10-phenanthroline-5,6-dione ligand with Zn(II), tris(1,10-phenanthroline-5,6-dione)zinc(II) hexafluorophosphate, [Zn(phen-dione)3](PF6)2, is reported. The complex was characterized by elemental analysis, IR, 1H NMR, electronic absorption spectroscopies, cyclic voltammetry and X-ray crystallography. Yellow crystals of [Zn(phen-dione)3](PF6)2 were formed by ether diffusion into an acetonitrile solution of the complex. The title complex crystallized in monoclinic crystal system (Z = 2) with space groups of P2 1, a = 12.0299(15) Å, b = 14.5306(19) Å, c = 13.1879(17) Å, β = 94.058(2)º and V = 2299.5(5) Å3. The structure was refined by using 10048 independent reflections, with I > 2σ(I) to an R factor of 0.0490. Single-crystal structure showed that the coordination geometry around the Zn(II) was a distorted octahedron. The complex showed an intense fluorescence band at visible region (690 nm) in CH3CN with an excitation wavelength of 310 nm at 25.0 ± 0.1 ºC. Cyclic voltammogram of the title complex showed two quasi-reversible reduction couples at negative potential, which were assigned to the consecutive reduction of phen-dione ligand to phen-semiquinonate and phen-diolate respectively by analogy to other phen-dione complexes at scan rate 200 mV s-1. 相似文献
15.
16.
Excess molar enthalpies, ?H m E , for the binary mixtures of butyl acetate + 1-alkanols, namely (methanol, ethanol, 1-propanol, 1-butanol, 1-pentanol, and 1-hexanol), were measured over the whole range of composition at 298.15 K using a Parr 1455 solution calorimeter. The excess partial molar enthalpies, ?H m,i E , were calculated from the experimental excess molar enthalpies using the Redlich–Kister polynomial equation. The sign of ?H m E for all systems are positive because of the disruption of hydrogen bonding and dipole–dipole interactions in the alkanols and esters, respectively. The magnitude of the ?H m E values increases with increasing alkyl chain length. The behavior of ?H m E was analyzed in terms of the length of the alkanol chain, the nature and type of intermolecular interactions and the balance between positive and negative effects on deviations from ideality. The experimental excess molar enthalpy data have also been correlated using the Redlich–Kister and SSF equations and two local composition models (UNIQUAC and NRTL). 相似文献
17.
NiFe2O4 nanoparticles are modified by graphene quantum dots (GQDs) and utilized to stabilize the Cu(II) nanoparticles as a novel magnetically retrievable catalytic system (Cu(II)/GQDs/NiFe2O4) for green formation of 4H‐pyrimido[2,1‐b]benzothiazoles. The prepared catalyst can be isolated assisted by an outer magnet and recovered for five courses without significant reduction in its efficiency. The as‐prepared magnetic heterogeneous nanocomposite was characterized by UV–Vis, FT‐IR, XRD, EDS, VSM, TEM, and ICP. Performing the reactions in environmentally friendly and affordable conditions (water), the low catalyst percentage, high yield of products, short reaction times, and easy workup are the merits of this protocol. 相似文献
18.
Abdollah Salimi Mohadeseh Izadi Rahman Hallaj Saied Soltanian Hassan Hadadzadeh 《Journal of Solid State Electrochemistry》2009,13(3):485-496
A simple procedure was developed to prepare a glassy carbon electrode modified with carbon nanotubes and Ruthenium (III) complexes.
First, 25 μl of dimethyl sulfoxide–carbon nanotubes solutions (0.4 mg/ml) was cast on the surface of the glassy carbon electrode
and dried in air to form a carbon nanotube film at the electrode surface. Then, the glassy carbon/carbon nanotube-modified
electrode was immersed into a Ruthenium (III) complex solution (direct deposition) for a short period of time (10–20 s for
multiwalled carbon nanotubes and 20–40 s for single-walled carbon nanotubes). The cyclic voltammograms of the modified electrode
in aqueous solution shows a pair of well-defined, stable, and nearly reversible redox couple, Ru(III)/Ru(II), with surface-confined
characteristics. The attractive mechanical and electrical characteristics of carbon nanostructures and unique properties and
reactivity of Ru complexes are combined. The transfer coefficient (α), heterogeneous electron transfer rate constants (k
s), and surface concentrations (Γ) for the glassy carbon/single-walled carbon nanotubes/Ru(III) complex-, glassy carbon/multiwalled carbon nanotubes/Ru(III)
complex-, and glassy carbon/Ru(III) complex-modified electrodes were calculated using the cyclic voltammetry technique. The
modified electrodes showed excellent catalytic activity, fast response time, and high sensitivity toward the reduction of
nicotinamide adenine dinucleotide in phosphate buffer solutions at a pH range of 4–8. The catalytic cathodic current depends
on the nicotinamide adenine dinucleotide concentration. In the presence of alcohol dehydrogenase, the modified electrode exhibited
a response to addition of acetaldehyde. Therefore, the main product of nicotinamide adenine dinucleotide electroreduction
at the Ru(III) complex/carbon nanotube-modified electrode was the enzymatically active NADH. The purposed sensor can be used
for acetaldehyde determination. 相似文献
19.
Kazem D. Safa Khatereh Ghorbanpour Akbar Hassanpour Shahin Tofangdarzadeh 《Journal of organometallic chemistry》2009,694(12):1907-1844
The Peterson olefination reaction of terephthalaldehyde with tris(trimethylsilyl)methyllithium, (Me3Si)3CLi, in Et2O gives disubstituted vinylbis(silane) 1 which reacts with MCPBA in CH2Cl2 at r.t. to afford mixture of mono and disubstituted epoxybis(silanes) 3 and 2. Vinylbis(silane) 1 can be completely converted into epoxybis(silane) 2 with an excess amount of MCPBA. The compound 2 was reacted with various reagents such as HX (X = Cl, Br), H2SO4, LiAlH4 and MeLi/CuI and give the related products. 相似文献