Search results for "Oct"
showing 10 items of 3052 documents
Coordination behavior of cinoxacine: Synthesis and crystal structure of tris (cinoxacinate) cobaltate(II) of sodium hexahydrate (HCx = 1-ethyl-4(1H) …
1991
The synthesis, crystal, and molecular structure of Co(Cx)3Na6H2O are reported. The Cobalt(II) compound crystallizes in the trigonal system, space group R 3 with Z = 6, in a cell of dimensions a= 18.688(7) (A), c= 20.142(6) A. Least-squares refinement of 1331 reflections [I≥3σ(I)] gave a final R = 0.088 for all observed reflections. The structure consists of anionic monomeric units of (Co(Cx)3−) and sodium cations. Three Cinoxacinate ions are chelated through Oceto and Ocarbox atoms. The Co(II) ion positioned on the third axis is bonded to six oxygen atoms in a slightly distorted octahedral environment.
Cyclometallation reactions in complexes of the type Rh(oq)(CO)[P(o-BrC6F4)Ph2]. The molecular structure of F4)Ph2] (oq = 8-hydroxyquinolinate)
1984
Cyclometallation occurs when a solution of the complex Rh(oq)(CO)(PCBr), (PCBr = 2-bromo-3,4,5,6-tetrafluorophenyldiphenylphosphine; oq = 8-hydroxyquinolinate) in toluene is refluxed, giving Rh(oq)2(PC) (PC = P(C6F4)(C6H5)2) and a dimeric compound, not yet completely characterized, formulated as Rh2Br(oq)(PCBr)2. Rh(oq)2(PC) was characterized by elemental analysis, by conductance measurements, and by 19F, 31P NMR and infrared spectroscopy. Its molecular structure was determined by single-crystal X-ray methods and refined by standard procedures to final agreement factors R and Rw of 0.067 and 0.060 for 5346 observed data. Lattice constants are 15.8494(6), 14.7188(5), 14.6675(5) A and β 96.93…
Oxidative DNA damage of mixed copper(II) complexes with sulfonamides and 1,10-phenanthroline
2003
Abstract Mixed coordination compounds of Cu(II) with sulfonamides and 1,10-phenanthroline as ligands have been prepared and characterised. Single crystal structural determination of the complex [Cu( N -quinolin-8-yl- p -toluenesulfonamidate) 2 (phen)] shows Cu(II) ions are located in a highly distorted octahedral environment, probably as a consequence of the Jahn–Teller effect. The FT-IR and electronic paramagnetic resonance (EPR) spectra are also discussed. The mixed complexes prepared undergo an extensive DNA cleavage in the presence of ascorbate and hydrogen peroxide. Two of the complexes have higher nucleolytic efficiency than the bis( o -phenanthroline)copper(II) complex.
Synthesis, crystal structures and magnetic properties of M(II)Cu(II) chains (M = Mn and Co) with sterically hindered alkyl-substituted phenyloxamate …
2011
A series of neutral oxamato-bridged heterobimetallic chains of general formula [MCu(L(x)2 (S)2] · p S · q H2O [p = 0-1, q = 0-2.5; L1 = N-2,6-dimethylphenyloxamate, S = DMF with M = Mn (1a) and Co (1b); L2 = N-2,6-diethylphenyloxamate, S = DMF with M = Mn (2a) and Co (2b) or S = DMSO with M = Mn (2c) and Co (2 d); L3 = N-2,6-diisopropylphenyloxamate, S = DMF with M = Mn (3a) and Co (3b) or S = DMSO with M = Mn (3c) and Co (3d)] were prepared by treating the corresponding anionic oxamatocopper(II) complexes [Cu(L(x))(2)]2- (x = 1-3) with M(2+) cations (M = Mn and Co) in DMF or DMSO as the solvent. The single-crystal X-ray structures of 2a and 3a reveal the occurrence of well-isolated, zigzag…
A magnetic self-contained thermochromic system with convenient temperature range
2019
A new ionic liquid with sugar-based ligand has been prepared and used to coordinate cobalt(II), at low loading, in an ionic liquid solution. The system obtained reveals magnetic switching and marked thermochromism in solution/polymer films over a convenient temperature range (20–60 °C). This system is self-contained, devoid of any volatile substances, and reproducible over multiple thermal cycles. The colour change can be attributed to a change in the coordination geometry from octahedral (pink) at room temperature to tetrahedral (blue) on warming, monitored by 59Co NMR spectroscopy, which was used for the first time to study the change. This material may find applications in stimuli-respon…
A giant hybrid organic-inorganic octahedron from a narrow rim carboxylate calixarene.
2020
Here we discovered an unprecedented giant octahedral coordination compound bearing 16 Zn2+, 12 Na+, 8 O2-, 4 OH-, 13 H2O and 6 L4- ligands [L4- = fully deprotonated tetra(carboxymethoxy)calix[4]arene]. Its structure was elucidated by single-crystal X-ray diffraction, wavelength-dispersive X-ray spectroscopy and MALDI-TOF mass spectrometry. This compound, Zn8Na6L6⊃Zn8Na6O8(OH)4(H2O)13 (external⊃internal), has eight tetrahedral zinc ions forming the coordination vertices of an outermost cube where carboxylate groups from the sodium calixarenes are anchored. Its core consists of eight Zn2+, six Na+, eight O2-, and four OH- distributed over three layers, besides thirteen coordinated H2O molecul…
Synthesis, characterization and catalytic properties for olefin polymerization of two new dimeric zirconium(IV) complexes having diamine-bis(phenolat…
2015
Abstract Reaction of the zirconium tetrachloride with one equivalent of the sodium salt of the diamine bis (phenolate) ligand, L1H2 (Me2NCH2CH2N-(CH2-2-OH-3,5-tBu-C6H2)2) or L2H2 (Me2NCH2CH2N-(CH2-2-OH-3,5-tBu-C6H2)(CH2-2-OH-C6H4)) in the presence of air led to formation of [Lig1ZrCl]2(μ-O) and [Lig2ZrCl]2(μ-O), respectively. These novel oxo-bridged dinuclear zirconium complexes were characterized by elemental analysis, 1H NMR spectroscopy and by single-crystal X-ray diffraction. Their reactivities in polymerization of ethylene and 1-octene, upon activation with Al(iBu)3/Ph3CB(C6F5)4 and MAO, were examined. It was found that lack of t-Bu substituents on one phenolate ring cause a significan…
Isobaric vapor-liquid equilibria for binary systems composed of octane, decane, and dodecane at 20 kPa
1996
Vapor−liquid equilibria were measured for binary systems of octane + decane, decane + dodecane, and octane + dodecane at 20.00 kPa using a recirculating still. The results are thermodynamically consistent according to the point-to-point consistency test, and deviation from ideal behavior is small for all systems.
Extraction Chromatographic Behavior of Rf, Zr, and Hf in HCl Solution with Styrenedivinylbenzene Copolymer Resin Modified by TOPO (trioctylphosphine …
2010
It is of great interest to study chemical properties of the transactinide elements with atomic numbers (Z) ≥ 104. One of the most important subjects is to establish the position of the elements at the extreme end of the periodic table. To this end we perform studies of chemical properties of these transactinides and compare them with those of their lighter homologues and with the ones expected from extrapolations in the periodic table. So far, chromatographic studies of the transactinides have provided experimental proof of placing rutherfordium (Rf, Z = 104) through hassium (Hs, Z = 108) into groups 4 to 8, respectively. 1-10 Quite recently, copernicium (Cn, Z = 112) has been shown to be a…
Slow Relaxation of the Magnetization in a {Co <sup>III</sup>Mn <sup>III</sup>} Heterometallic Brick-Wall Network
2021
The use of the cyanide-bearing dicobalt(III) complex (PPh 4 ) 2 [Co 2 III (m-2,5-dpp)(CN) 8 ] as a metalloligand towards [Mn(salen)(H 2 O)]ClO 4 afforded the heterobimetallic two-dimensional compound of formula [{Mn III (salen)} 2 {(m-NC) 4 Co 2 III (m-2,5-dpp)(CN) 4 }] n (1) [PPh 4 + = teraphenylphosphonium cation, 2,5-dpp = 2,5-bis(2-pyridyl)pyrazine and H 2 salen = N,N’ -ethylenebis(salicylideneimine)] whose structure has been determined by single crystal X-ray diffraction. Compound 1 exhibits a neutral brick-wall structure, where each [Co 2 III (m-2,5-dpp)(CN) 8 ] 2- unit adopts a tetrakis-monodentate bridging mode towards four {Mn III (salen)} + fragments through four of its eight cyan…