Synthesis, characterization and biomedical activities of molybdenum complexes of tridentate Schiff base ligands. Crystal and molecular structure of [MoO2(L10)(DMSO)] and [MoO2(L11)(DMSO)]

Synthesis, characterisation and biological activities of S-2- or S-4-methylbenzyl-β-N-(di-2-pyridyl)methylenedithiocarbazate and Cu(II), Ni(II), Zn(II) and Cd(II) complexes

“…The coordination of these compounds often lead to enhanced biological activity in several pathogenic fungi [3,[19][20][21]. Some of these metal complexes have been known to accelerate drug action and the efficacy of a therapeutic agent [1][2][3][4][5][6][19][20][21].The Schiff bases synthesized in this study are the di-2-pyridylketone Schiff bases of isomeric dithiocarbazates, S-2-methylbenzyldithiocarbazate, S-3-methylbenzyl dithiocarbazate and S-4-methylbenzyldithiocarbazate (Fig. 1).…”

Synthesis and Evaluate of Some New 1,2,4-Triazoles to Modify Epoxy Resins in the Field of Anti-Microbial and Anti-Corrosive Organic Coating.

“…This is supported by the appearance a peak at 659 cm −1 in the metal complexes due to ν(C-S) (33) . The third feature is that the appearance of broad band at 3401cm −1 which can be assigned to the stretching frequencies of ν(OH) of water molecules either in the coordinated or uncoordinated form associated to the complexes which are also confirmed by thermal analyses as well as appearance of the non-ligand band at 554 cm −1 assignable to ν(M-O) (34,35) .…”

Synthesis, Characterization and Biological Studies of Novel Schiff Base viz. Bis-1,1'-(pyridine-2,6-diyldieth-1-yl-1-ylidene) biguanidine and Their Transition Metal Complexes

“…A. niger and Trichophyton rubrum were sensitive towards all of the test compounds. It was observed that by the application of the all test compounds the growth was inhibited with some variations [41]. Either the impermeability of the cells of the fungus or the difference of the ribosomes of fungal cells may be the cause of the variation in the effectiveness of different compounds against different fungi [42].…”