scholarly journals THE CHELATING POLYIMINE BASED ON P-PHENYLENEDIAMINE AND GLYOXAL

2020 ◽  
Vol 18 (4) ◽  
pp. 445-450
Author(s):  
S.Z. Ismayilova ◽  
Keyword(s):  
Transition Metals ◽  
Elemental Analysis ◽  
Electron Spectroscopy ◽  
Molar Ratio ◽  
Composition And Structure ◽  
Chelating Ability

Condensation of p-phenylenediamine and glyoxal at a molar ratio of 1: 1 made it possible to synthesize a new polyimine with chelating ability. The complexation of this polyimine with transition metals was studied and the composition and structure of the complexes obtained were explored by means of IR, electron spectroscopy, EPR, derivatography, and elemental analysis.

scholarly journals SYNTHESISAND STUDY OF THE COMPLEXES OF: N-(3,4,5-TRIMETHOXY PHENYL)-N- BENZOYL THIOUREA (TMPBT) WITH A NUMBER OF TRANSITION METALS AND THEIR INDUSTRIAL AND MEDICAL IMPORTANCE

2020 ◽  
Vol 12 (2) ◽  
pp. 62-70
Author(s):  
أمير حسين حسن ◽  
Keyword(s):  
Transition Metals ◽  
Atomic Absorption ◽  
Elemental Analysis ◽  
Ph Effect ◽  
Structural Formula ◽  
Effect Study ◽  
Uv Spectra ◽  
Molar Conductivity ◽  
Molar Ratio ◽  
Medical Importance

This paper performance for preparation and identification of six new complexes of a number of transition metals Cr (lII), Mn (I1), Fe (l), Co (II), Ni (I1), Cu (Il) with: N - (3,4,5-Trimethoxy phenyl-N - benzoyl Thiourea (TMPBT) as a bidentet ligand. The prepared complexes have been characterized, identified on the basis of elemental analysis (C.H.N), atomic absorption, molar conductivity, molar-ratio ,pH effect study, I. Rand UV spectra studies. The complexes have the structural formula ML2X3 for Cr (III), Fe (III), and ML2X2 for Mn (II), Ni (II), and MLX2 for Co (Il) , Cu (Il).

scholarly journals Synthesis, Characterization, and Electrochemical Behaviour of Cobalt(II) and Nickel(II) Complexes with N2O2 Chelating Ligand 4,4′-(Biphenyl-4,4′-diyldinitrilo)dipentan-2-one

2013 ◽  
Vol 2013 ◽  
pp. 1-11 ◽  
Author(s):  
Lakhdar Sibous ◽  
Embarek Bentouhami ◽  
Mustayeen Ahmed Khan
Keyword(s):  
Schiff Base ◽  
Mass Spectroscopy ◽  
Elemental Analysis ◽  
Electrochemical Behaviour ◽  
Absolute Ethanol ◽  
Molar Ratio ◽  
H Nmr ◽  
Chelating Ligand ◽  
Metal Ligand

4,4′-Diaminobiphenyl reacts with 2,4-pentanedione in absolute ethanol in a molar ratio 1 : 2 to form mainly the product of [1 + 2] condensation, 4,4′-(biphenyl-4,4′-diyldinitrilo)dipentan-2-one (H2L). The Schiff base was used as tetradentate chelating ligand to coordinate CoII and NiII chlorides leading to complexes where the ratio of metal ligand was found to be 2 : 1 or 2 : 2. All the synthesized products were characterized by elemental analysis, infrared, electronic, and mass spectroscopy, 1H NMR, and DSC. The electrochemical behaviour of the ligand and its complexes in DMF is also investigated.

Bimetallic Group 6 Tricarbonyls Triply-Bridged by Bis(phenylthio)alkane Bidentate Ligands

2010 ◽  
Vol 93-94 ◽  
pp. 13-16
Author(s):  
Khalil J. Asali
Keyword(s):  
1H Nmr ◽  
Elemental Analysis ◽  
Thermodynamic Stability ◽  
Chlorinated Hydrocarbons ◽  
Metal Center ◽  
Molar Ratio ◽  
Bidentate Ligands ◽  
Group 6 ◽  
Ft Ir

Reactions of the labile complex (Me3tach)M(CO)3 (Me3tach = 1,3,5-trimethyl-1,3,5-triazacyclohexane; M = W, Mo) with bis(phenylthio)alkanes ( = PhS(CH2)nSPh), (2:3 molar ratio) in CH2Cl2 as solvent (at 35 oC M = W, 0 oC M = Mo) afforded in good yields bimetallic tricarbonyl complexes triply- bridged by bis(phenylthio)alkanes of the type [M(CO)3]2(μ-PhS-(CH2)n-SPh)3 [n = 3 (a), 4 (b), 5 (c), 6 (d); M = W (1), Mo (2)]. These new triply-bridged complexes were characterized by 1H NMR, FT-IR and elemental analysis. Additionally, it has been observed that the thermodynamic stability of some of these new complexes in chlorinated hydrocarbons depends mainly on the nature of the metal center and varies in the order W >> Mo.

scholarly journals STUDY OF THE PROCESS OF OXIDATIVE DESULFURIZATION OF DIESEL FUEL IN THE PRESENCE OF CO-CATALYSTS

2021 ◽  
pp. 88-96
Author(s):  
D. Muktaly ◽  
◽  
Zh.K. Myltykbaeva ◽  
M.B. Smaiyl ◽  
◽  
...  
Keyword(s):  
Sulfuric Acid ◽  
Transition Metals ◽  
Diesel Fuel ◽  
Oxidation Process ◽  
Oxidative Desulfurization ◽  
Sodium Molybdate ◽  
Molar Ratio ◽  
Petrochemical Plant ◽  
Continuous Growth ◽  
Diesel Fractions

Continuous growth in consumption of oil in the world, as well as ever-increasing quality requirements stimulate the search for new scientific and technological solutions to directionally affect the characteristics of petroleum products, including their chemical composition. The advantages of oxidative desulfurization before hydrotreating are the absence of the need to use hydrogen, as well as small capital and energy costs, since the method does not require high temperatures and pressures. The purpose of this work was to study the oxidation process of diesel fuel and to search for the optimal mode of oxidative desulfurization of diesel fuel in the presence of transition metals salts with the addition of mineral acids. The object of the study is a straight-run diesel fraction of the Pavlodar Petrochemical Plant with boiling temperatures of 180-350°C. The oxidation process was carried out with hydrogen peroxide in the presence of salts of the transition metals molybdenum, vanadium and tungsten. The article defined the basic physico-chemical characteristics of straight-run and desulfurized diesel fractions. The optimal catalyst (Na2MoO4) was selected at a molar ratio of metal to sulfur of 1:100 for the oxidation process of straight-run diesel fractions. As a result of oxidative desulfurization of diesel fuel in the presence of sodium molybdenum perox complexes, the total sulfur content decreased by 42.9%, and with the addition of sulfuric acid by 56.5%. An increase in the cetane index from 56.3 to 58.6 was revealed in the presence of sodium molybdate with the addition of sulfuric acid.

scholarly journals An N4-Tetradentate Hydrazone Ligand That Binds in a Neutral, Mono- and Bisdeprotonated Form to Iron(II) and Zinc(II) Metal Ions

Crystals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 982
Author(s):  
Devaraj Pandiarajan ◽  
Thomas Fox ◽  
Bernhard Spingler
Keyword(s):  
Mass Spectrometry ◽  
Coordination Chemistry ◽  
Transition Metals ◽  
Metal Ions ◽  
Elemental Analysis ◽  
X Ray Diffraction ◽  
Hydrazone Ligand ◽  
X Ray

The coordination chemistry of butane-2,3-dione bis (2′-pyridylhydrazone) towards the divalent first-row transition metals zinc and iron has been explored. Depending upon the conditions, the ligand in the six complexes was found to be either neutral, mono, or doubly deprotonated. The zinc(II) and iron(II) complexes were fully characterized by elemental analysis, mass spectrometry, and X-ray diffraction methods.

Phosphor- und Schwefelhydrazin-Verbindungen / Phosphorus- and Sulfurhydrazine-Compounds

1971 ◽  
Vol 26 (12) ◽  
pp. 1232-1235 ◽  
Author(s):  
Herbert W. Roesky ◽  
Olaf Petersen
Keyword(s):  
Ir Spectra ◽  
Elemental Analysis ◽  
Mass Spectra ◽  
Molar Ratio ◽  
H Nmr ◽  
Chemical Behaviour

Pyrosulfonyldifluoride reacts with waterfree hydrazine in a molar ratio of 2 : 3 to give hydrazine -1,2-bis(sulfonylfluoride) in a low yield.. The reaction of N-fluorosulfonylamide and SOCl2 yields NH4⊕⊖ N(SO2F)2. This salt is converted to (C6H5)4P⊕⊖N(SO2F)2 in water by (C6H5)4PCl. (CH3)2NNH2 reacts with PSF3, PSF2Br, PSF2CH3 or PSF2C2H5 to yield the following compounds: (CH3)2NNHPSF2, (CH3)2NN (PSF2)2, (CH3)2NNHPSFCH3 and (CH3)2NNHPSFC2H5. The properties and the chemical behaviour of these substances are described. Results of ir-spectra, as well as 31P-, 19F- and 1H-nmr- and mass-spectra and elemental analysis characterize the compounds.

Synthesis of zirconocene silsesquioxane complexes and their ethene polymerization activity in systems with methylaluminoxane

2010 ◽  
Vol 75 (1) ◽  
pp. 105-119 ◽  
Author(s):  
Vojtech Varga ◽  
Jiří Pinkas ◽  
Róbert Gyepes ◽  
Petr Štěpnička ◽  
Michal Horáček ◽  
...  
Keyword(s):  
Ir Spectra ◽  
Elemental Analysis ◽  
Molar Ratio ◽  
Stoichiometric Ratio ◽  
Polyhedral Oligomeric Silsesquioxanes ◽  
Xps Spectra ◽  
Zirconocene Dichloride ◽  
Order Of Magnitude ◽  
Ethene Polymerization

Protocols for obtaining defined zirconocene complexes with polyhedral oligomeric silsesquioxanes with mono-, di-, and trisilanol functionality (SIPOSS, DIPOSS, and TRIPOSS) were established. The TRIPOSS silanolates binding one zirconocene and one chlorozirconocene moiety, [{(c-C5H9)7Si7O9O3}Zr2Cl(η5-C5H4R)4] (1, R = Bu; 2, R = H), were obtained by reacting the silanol with the respective zirconocene dichloride and triethylamine in CH2Cl2 in a 1.0:3.0:3.0 molar ratio, an excess of the zirconocene dichloride being required to suppress intramolecular dehydration of TRIPOSS. The related SIPOSS complex, [{(c-C5H9)7Si8O12O}2Zr(η5-C5H4Bu)2] (3), was prepared similarly at the stoichiometric ratio of [ZrCl2(η5-C5H4Bu)2]/ SIPOSS/NEt3 equal to 1.0:2.0:2.0. When employed in the 1.0:1.0:1.0 ratio, the same reagents afforded only the impure complex [{(c-C5H9)7Si8O12O}ZrCl(η5-C5H4Bu)2] (4), contaminated with 3 and unreacted [ZrCl2(η5-C5H4Bu)2]. Finally, the zirconocene complexes with SIPOSS and DIPOSS moiety, [{(c-C5H9)7Si8O12O}2Zr(η5-C5H5)2] (5) and [(c-C5H9)7Si7O9(OSiMe3)O2}- Zr(η5-C5H5)2] (6), respectively, were obtained by reacting [ZrMe2(η5-C5H5)2] with stoichiometric amounts of the appropriate silanols. All complexes were characterized by 1H, 13C, 29Si NMR and IR spectra, and by elemental analysis from XPS spectra. Preliminary ethene polymerization experiments showed that compounds 5 or 6 when combined with an excess of methylaluminoxane were nearly as active as [ZrCl2(η5-C5H5)2] whereas compound 2 was by about one order of magnitude less active.

scholarly journals Cr(III),Mn(II),Fe(III),Co(II),Ni(II),Cu(II) and Zn(II) Complexes with Diisobutyldithiocarbamato Ligand

2011 ◽  
Vol 8 (4) ◽  
pp. 2020-2023 ◽  
Author(s):  
Mohammad Tarique
Keyword(s):  
Transition Metals ◽  
Spectral Data ◽  
Elemental Analysis ◽  
Coordination Compounds ◽  
Analytical Data ◽  
Spectral Studies

The synthesis of sulphur and nitrogen containing dithiocarbamato ligand derived from diisobutylamine as well as its coordination compounds with 3d series transition metals is presented. These synthesized compounds were characterized on the basis of elemental analysis, conductometric measurements and IR spectral studies. The analytical data showed the stoichiometry 1:2 and 1:3 for the compounds of the types ML2{M=Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)} and M'L3{M'=Cr(III) and Fe(III)} respectively. The conductometric measurements proved the non-electrolytic behaviour of all the compounds. The bidentate nature of dithiocarbamato moiety was confirmed on the basis of IR spectral data.

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