Sharif Digital Repository

The novel unsymmetrical, diimino-tetradentate Schiff bases derived from 2-[(2-amino-phenylimino)- methyl]-phenol and 2-[1-(2-amino-phenylimino)-ethyl]-phenol were synthesised and characterised by template and non-template methods  

Graphene oxide was an effective supporting material for immobilizing a dioxomolybdenum Schiff base complex via covalent interaction. The large surface of graphene oxide plays important roles to obtain a good degree of catalytic reaction. Catalytic capacity of the graphene-bound dioxomolybdenum Schiff base complex was investigated for the oxidation of various sulfides to sulfoxide compounds using hydrogen peroxide urea as an oxidant. The catalyst was characterized by various techniques including XRD, FTIR, TGA, SEM, UV–vis, and ICP-AES. The immobilized complex was very efficient with the extra benefits of easy recovery and recycling of the heterogeneous catalyst. The graphene oxide bound... 

The novel unsymmetrical tetradentate Schiff base complexes of Co(II) and Pd(II) with the general formula M(SaI.Phen.Acac.) and M(Sal.Phen. Naph.), have been synthesised by template and non-template method  

The reaction of a solution of MoO2(acac)2 in CH3OH and salicylidene 2-picoloyl hydrazone as a tridentate ONO donor Schiff base (ONO) afford a six-coordinated Mo(VI) complex [MoO2(ONO)(CH3OH)], with a distorted octahedral configuration. [MoO2(ONO)(CH3OH)] was isolated as an air-stable crystalline solid and fully characterized by single-crystal X-ray structure analysis. [MoO2(ONO)(CH3OH)] shows reactivity in the oxidation of sulfides to their corresponding sulfoxides using urea hydrogen peroxide as the oxidant at room temperature under air  

Molybdenum complexes bearing a salicylidene 2-picoloyl hydrazone ligand have been synthesized and characterized. The salicylidene 2-picoloyl hydrazone ligand (H2sal-phz) was prepared by reaction of picoloyl hydrazine with salicylaldehyde. Reaction of H2sal-phz with MoO2(acac) 2 generates the dioxo molybdenum complex MoO2(sal-phz) (CH3OH). Treatment of MoO3 in the presence of H 2O2 with H2sal-phz produces the oxo-peroxo molybdenum(VI) complex MoO(O2)(sal-phz)(CH3OH). The new compounds were characterized by 1H NMR and IR spectroscopies, and elemental analysis. The complexes were also characterized by single crystal X-ray diffraction crystallography. The complexes were evaluated for epoxidation... 

Three ternary copper(II) complexes [Cu(5-bromo-salTyr)(bipy)]·1/ 2CH3OH (1), [Cu(5-bromo-salLue)(bipy)]·CH3OH (2) and [Cu(5-bromo-salTrp)(bipy)]·3CH3OH (3) (where 5-bromo-salTyr, 5-bromo-salLue and 5-bromo-salTrp are tridentate Schiff base ligands derived from the condensation of 5-bromosalicylaldehyde with tyrosine, leucine and tryptophan, respectively, and bipy is 2,2′-bipyridine) have been prepared and characterized by elemental analysis, electronic, IR spectroscopies, magnetic measurement and cyclic voltammetry. The complexes, 1 and 3 have been also structurally characterized by X-ray diffraction technique. Crystal structures of 1 and 3 complexes displayed a distorted square-pyramidal... 

The Mn-hydrazone Schiff base has been prepared, characterized, and encapsulated into NaY to prepare a new heterogeneous catalyst. Elemental analysis, UV-Vis, infrared spectroscopic analysis, diffuse reflectance spectroscopy, thermal analysis, small angle X-ray diffraction, and N2 sorption indicate the presence of Mn-hydrazone Schiff base within the nanocavity pores of zeolite-Y. The catalysts showed excellent catalytic efficiency in epoxidation with various olefinic compounds including cyclooctene, using tert-BuOOH as oxidant. Cyclooctene showed high conversion (97%) as well as epoxide selectivity (89%) with tert-BuOOH. Moreover, the encapsulated complex showed good recoverability without... 

A new hydrazone-Schiff base (H2L) and it corresponding dioxomolybdenum(VI) complex were synthesized and characterized by spectroscopic methods and elemental analyses. The crystal structures of both ligand and its complex were determined by single-crystal X-ray diffraction. A new hydrazone Schiff base, (E)-N′-(3-ethoxy-2-hydroxybenzylidene)isonicotinohydrazide (H2L), has been prepared and characterized by elemental analyses, spectroscopic methods, and single-crystal X-ray diffraction. The corresponding dioxomolybdenum(VI) complex [Mo(O)2(L)(CH3OH)] was synthesized and characterized by spectroscopic methods and by single-crystal X-ray diffraction. The hydrazone ligand coordinates to Mo through... 

The monoanionic bidentate Schiff base, N-(phenolyl)-benzaldimine (HL), has been employed to synthesize a new vanadium(IV) complex of general composition [VO(L)2] (where L = O, N donor of Schiff base). The ligand and complex have been fully characterized by elemental analyses, molar conductance data, FT-IR, 1H- and 13C-NMR, and UV-Vis spectroscopies. Oxidation of alcohols to their corresponding aldehydes and ketones was conducted by this complex catalyst using Oxone as oxidant under biphasic reaction conditions (CH2Cl2/H2O) and tetra-n-butylammonium bromide as phase transfer agent under air at room temperature  

The non-symmetrical tetradentate Schiff-base H2L have been obtained using the half-unit N-(1-hydroxy-2-acetonaphthone)-1-amino-2- phenyleneimine (HL1) with 2-hydroxyl-1-naphthaldehyde. ML complexes(M = Ni(1), Cu(2), Co(3) and Zn(4)) were prepared and characterized by atomic absorption, IR, UV, 1H NMR spectroscopy, and a single crystal X-ray structure. Crystal data for (1) are triclinic space group P-1, a = 7.9784 (3) A, b = 10.2417 (4) A, c = 13.4090 (5) A, α = 103.8480 (10)°, β = 97.0540 (10)°, γ = 92.2400 (10)° and z = 2. Crystal data for (2): Triclinic space group P-1, a = 7.9991 (6) A, b = 10.0520 (7) A, c = 13.6974 (10) A, α = 103.6500 (10)°, β = 95.9650 (10)°, γ = 90.3160 (10)° and z =... 

A heterogeneous nanocatalyst was prepared via covalent anchoring of dioxomolybdenum(VI) Schiff base complex on core-shell structured Fe3O4@SiO2. The properties and the nature of the surface-fixed complex have been identified by a series of characterization techniques such as SEM, EDX, XRD, TGA, FT-IR, and VSM. The synthesized hybrid material was an efficient nanocatalyst for selective oxidation of olefins to corresponding epoxides with t-BuOOH in high yields and selectivity. The catalyst could be conveniently recovered by applying an external magnetic field and reused several times without significant loss of efficiency. © 2016 Taylor and Francis  

Two unique heteronuclear Schiff base complexes of Cu(II), [{Cu(L)Na(ClO4)}2(μ-H2L)] (1) and Ni(II), [{Ni(L)Na(BF4)}2(μ-H2L)] (2) were synthesized and characterized by different spectroscopic methods as well as X-ray crystallography. The Schiff base ligand (H2L) was synthesized from the condensation meso-1,2-diphenyl-1,2-ethylenediamine with 3-methoxysalicylaldehyde. The 3d metal ions in these complexes have been accommodated by the inner N2O2 compartment of the Schiff base ligand, while the O2O′2 outer compartment has accommodated the Na(I) ion (O and O′ denote the phenolic and methoxy oxygen atoms, respectively). Besides, a Schiff base ligand has doubly bridged the M(II)/Na(I) moieties via... 

An hydrazone Schiff base-iron(III) complex using salicylidene benzoyl hydrazine (L) as ligand has been synthesized and characterized by elemental analyses, IR, 1H and 13C NMR and UV-Vis spectroscopy. Oxidation of sulfides to sulfoxides in one-step was conducted by this complex catalyst using urea hydrogen peroxide (UHP) in mixture of CH2Cl2/CH3OH (1:1) under air at room temperature. The effect of the reaction conditions on the oxidation of methylphenylsulfide was studied by varying the amount of the catalyst, reaction temperature, reaction time and the amount of UHP. The results showed that using this system in the oxidation of sulfides, sulfoxides were obtained as the main products,... 

The synthesis of a Mo(VI) Schiff base complex, cis-[MoO2{(4,6-bis(tert-butyl)-2-{(benzyl)iminomethyl}phenolate)2}], cis-[MoO2(L)2] where L = 4,6-bis(tert-butyl)-2-{(benzyl)iminomethyl}phenol, derived from benzylamine and 3,5-di-tert-butylsalycilaldehyde is reported. Full characterization of this complex was accomplished with elemental analyses, spectroscopic studies (NMR, IR and electronic) and X-ray structure analysis. This complex was tested as a catalyst for the homogeneous oxidation of olefins. The Mo(VI) complex is catalytically active for the epoxidation of aliphatic substrates at 80 °C, yielding the epoxide as the sole product in yields up to 100% and turnover numbers up to 5000.... 

We have explored the suitability of an O,N,N–donor Schiff base (H2SB) for obtaining dinuclear complexes with heavy metal ions such as Cu2+, Zn2+, Ni2+, and Co2+ (borderline acids) as well as Pd2+ and Cd2+ (soft acids). Spectroscopic studies demonstrated that the complexation of H2SB and Cu2+, Zn2+, Ni2+, Co2+, Pd2+, and Cd2+ occurred at a 1:1 stoichiometry. We have found two square planar centers with Pd-N-Pd angles of 93.08(11)◦ and a Pd–Pd distance of 3.0102(4) Å in Pd2(SB)2·Me2CO. This Pd–Pd distance is 30% shorter than the sum of the van der Waals radii, which is in accordance with a strong palladophilic interaction. Fluorescence studies on H2SB-M2+ interaction showed that H2SB can... 

Reaction of 2-pyridinecarboxaldehyde with L-Alaninol (as a chiral amine) or 2-amino-2-methyl-1-propanol (AMP) in the presence of PdCl2 produced the new and attractive palladium(II) complexes which were synthesized by in situ method. The presence of an extra methyl group in AMP other than L-Alaninol induced the different chelating mode and, therefore, several structurally different palladium complexes obtained. Correspondingly, the chiral amine with PdCl2 produced the imine product, (Iminol (1)), and an oxazolidine compound (Imizol (1′)) as minor product. Also, the use of AMP in formation of palladium complexes led to the synthesis of imine (Ampynol (2)) and oxazolidine (Ampyzol (3))... 

Two new potentially heptadentate N4O3 Schiff base ligands {N[(CH2)3NCH(2-OH-3,5-t-Bu2C 6H2)]3} (H3L1) and {N[(CH2)3NCH(2-OH-3,5-t-Bu2C6H 2)]2 [(CH2)2-NCH(2-OH-3,5-t-Bu 2C6H2)]} (H3L2) were synthesized and characterized by various spectroscopic methods. The heptadentate N4O3 Schiff bases, H3L1 and H 3L2, were derived from the condensation reaction of two tripodal tetraamine ligands, tris(3-aminopropyl)amine and (2-aminoethyl)-bis(3- aminopropyl)amine with 3 equiv. of 3,5-di-tert-butylsalicylaldehyde, respectively. The neutral gadolinium(III) and samarium(III) complexes, [Ln(L)], of these bulky ligands and also a gadolinium(III) complex of a previously known ligand,... 

Aryl schiff bases were efficiently reduced to the corresponding secondry amines by triethylammonium formate/formic acid system under microwave irradiation in solvent-free condition  

Two series of the novel unsymmetrical diimino tetradentate Schiff bases derived from phenylenediamine and 1,3-naphthalene diamine and their vanadyl complexes were synthesized by template and non-template methods and characterized by 1H, 13C NMR, IR, UV-Vis and elemental analysis. These complexes are used as catalysts for the selective aerobic oxidation of cyclohexene. The catalytic activity increases as the number of electron-donor groups decreases, and the catalytic selectivity is varied by changing the substituents on the ligands. The catalytic system described here is an efficient and inexpensive method for the oxidation of olefins, with the advantages of high activity, selectivity,... 

Novel vanadyl Schiff base complexes with the general formula VOLx (x = 7-18) were synthesized and characterized by physicochemical methods. Only an orange polymeric form was obtained for VOL13, both brown polymeric and green monomeric forms were obtained for VOLx, x = 16, 17. These observations suggest that in these complexes oxovanadium(IV) exhibit a coordination number of five. Systematic substitution on the ancillary ligand have allowed V(V)/V(IV) reduction potentials to be tuned over a range of approximately 130mV. The complexes are catalysts for the aerobic oxidation of cyclohexene. Catalytic activity increases with increasing V(V)/V(IV) reduction potential and the catalytic selectivity...