53364-10-6

Upstream product

• 90-02-8 salicylaldehyde 
• 496-72-0 4-methyl-1,2-diaminobenzene 

Relevant academic research and scientific papers

Study the biological effect of nanosize ferric oxides prepared from low cost organic materials against human breast cancer cells

The aim of this paper is to fully exploit the medical potential of α?Fe2O3 as a promising material for anticancer agent. Herein, Fe2O3 nanoparticles (NPs) have been synthesized using thermal decomposition method

Synthesis and spectroscopic characterization of Zr(IV) and Th(IV) with chelating containing ONNO donor quadridentate Schiff bases complexes

New metal complexes of novel Schiff bases derived from the reaction of zirconium (IV) and thorium (IV) ions with N,N′-disalicylidene-l,2-phenylenediamine (H2dsp), N,N′-disalicylidene-3,4-diaminotoluene (H2dst), 4-nitro-N,N-disalicyli

Syntheses and characterization of Ru(III) with chelating containing ONNO donor quadridentate Schiff bases

Complexes of ruthenium(III) with N,N′-disalicylidene-l,2-phenylenediamine (H2dsp), N,N′-disalicylidene-3,4-diaminotoluene (H2dst), 4-nitro-N,N′-disalicylidene-1,2-phenylenediamine (H2ndsp) and N,N′-disalicylidene ethylened

Solvent-free cycloaddition of CO2 and propylene oxide to cyclic carbonates using different ligand metal complexes

Tetradentate ligand metal complexes salen-Co(III)OBzF5, salen-CH3Co(III)OBzF5, salen-CH3Co(III)Br, and salen-ClCo(III)Br were synthesized. These complexes were used as catalysts for the chemical fixation of COs

A New Approach in Cancer Treatment: Discovery of Chlorido[ N, N′-disalicylidene-1,2-phenylenediamine]iron(III) Complexes as Ferroptosis Inducers

Chlorido[N,N′-disalicylidene-1,2-phenylenediamine]iron(III) complexes generate lipid-based ROS and induce ferroptosis in leukemia and neuroblastoma cell lines. The extent of ferroptosis on the mode of action is regulated by simple modifications of the sub

Synthesis, structure and catalytic alcohol oxidation by ruthenium(III) supported by Schiff base and triphenylphosphine ligands

Treatment of [RuCl2(PPh3)3] with two equiv. bi-dentate Schiff base N,O-LH-Cl (N,O-LH-Cl = 2[(3-chloro-phenylimino)-methyl]-phenol) or N,O-LH-NO2 (N,O-LH-NO2 = 2[(4-nitro-phenylimino)-methyl]-phenol) in the presence of triethylamine afforded cis-[RuCl(PPh3)(κ2-N,O-L-Cl)2] (1) and trans-[RuCl(PPh3)(κ2-N,O-L-NO2)2]·Et2O (2), respectively. Reactions of [RuCl2(PPh3)3] and equal equiv. tetra-dentate Schiff bases gave corresponding ruthenium(III) complexes [RuCl(PPh3)(salen)] (3) (H2salen = N,N′-disalicylidene-1,2-ethanediamine), [RuCl(PPh3)(salipn)]·2CH2Cl2 (4) (H2salipn = N,N′-disalicylidene-1,2-(1-methyl)ethanediamine), [RuCl(PPh3)(salpn)]·CH2Cl2 (5) (H2salpn = N,N′-disalicylidene-1,2-propanediamine), [RuCl(PPh3)(salphen)]·CH2Cl2 (6) (H2salphen = N,N′-disalicylidene-1,2-phenyldiamine), [RuCl(PPh3)(saltoln)]·CH2Cl2 (7) (H2saltoln = N,N′-disalicylidene-1,2-tolyldiamine) and [RuCl(PPh3)(salcyn)] (8) (H2salcyn = N,N′-disalicylidene-(R,R)-1,2-cyclohexanediamine). The molecular structures of complexes 1–5 and 7 have been determined by single-crystal X-ray crystallography. The catalytic oxidation properties of ruthenium(III) complexes 1–8 were tested towards alcohols in the presence of N-methylmorpholine-N-oxide.

Effect of the substitutional groups on the electrochemistry, kinetic of thermal decomposition and kinetic of substitution of some uranyl Schiff base complexes

Uranyl(VI) complexes, [UO2(X-saloph)(solvent)], where saloph denotes N,N'-bis(salicylidene)-1,2-phenylenediamine and X = NO2, Cl, Me, H; were synthesized and characterized by 1H NMR, IR, UV-Vis spectroscopy, thermal gravim