scholarly journals Synthesis, Characterization and Antimicrobial Activity of Cu(II), Co(II) and Ni(II) Complexes with O, N, and S Donor Ligands

2008 ◽  
Vol 5 (3) ◽  
pp. 577-583 ◽  
Author(s):  
Vidyavati Reddy ◽  
Nirdosh Patil ◽  
S. D. Angadi
Keyword(s):  
Schiff Base ◽  
Magnetic Measurements ◽  
Antimicrobial Activities ◽  
Octahedral Geometry ◽  
Donor Ligands ◽  
Azomethine Nitrogen ◽  
Spectral Studies ◽  
Conductivity Measurements ◽  
Schiff Base Ligands ◽  
Plate Method

The complexes of the type ML2[where M = Cu(II), Co(II), and Ni(II)] L = 1-phenyl-1-ene-3-(2-hydroxyphenyl)-prop-2-ene with 3- substituted-5-mercapto-4-amino-1,2,4-triazoles. Schiff base ligands have been prepared by reacting 3-(2-hydroxyphenyl)-1-phenylprop-2-en-1-one and 3-phenyl/pyridyl-4-amino-5-mercapto-1,2,4-triazoles in an alcoholic medium. The complexes are non-electrolytes in DMF. The resulting complexes were characterized by elemental analysis, magnetic measurements, conductivity measurements and spectral studies. The Schiff base acts as a tridentate dibasic and coordinating through the deprotonated oxygen, thioenolic sulphur and azomethine nitrogen atoms. It is found that Cu(II), Co(II), and Ni(II) complexes exhibited octahedral geometry. The antimicrobial activities of ligands and its complexes were screened by cup plate method.

scholarly journals Some Organotellurium(IV) Complexes of 1-Methyl-3-(p-tolylimino)indolin-2-one Schiff Base

2021 ◽  
Vol 33 (6) ◽  
pp. 1236-1244
Author(s):  
Manish Kumar ◽  
K.K. Verma ◽  
Sapana Garg
Keyword(s):  
Schiff Base ◽  
Xanthomonas Campestris ◽  
Computational Study ◽  
Molar Conductance ◽  
Bidentate Ligand ◽  
Octahedral Geometry ◽  
Azomethine Nitrogen ◽  
Spectral Studies ◽  
Distorted Octahedral Geometry ◽  
No Donor

Six new hexa-coordinated organotellurium(IV) complexes of type RTeCl3·NMeIPT and R2TeCl2·NMeIPT (R = 4-hydroxyphenyl, 4-methoxyphenyl or 3-methy-4-hydroxyphenyl; NMeIPT(L) = Schiff base (1-methyl-3-(p-tolylimino)indolin-2-one) derived from condensation of 4-methylisatin and p-toluidine) have been synthesized and characterized by different spectral studies like elemental analyses, molar conductance, infrared, mass spectrometry, 1H NMR, 13C NMR and UV-visible spectroscopy. On the basis of spectroscopic data, it is evident that Schiff base behaves as NO donor bidentate ligand via azomethine nitrogen atom and oxygen atom from carbonyl group for all the tellurium(IV) complexes. The results showed that all the organotellurium(IV) complexes possess distorted octahedral geometry. Geometry of the all organotellurium(IV) complexes was optimized and their theoretical quantum mechanical parameters were calculated. This computational study also suggests octahedral geometry for complexes. The antimicrobial activity of NMeIPT and all the organotellurium(IV) complexes were screened against bacteria i.e. Xanthomonas campestris and Bacillus cereus and fungi i.e. Fusarium oxysporum, Candida albicans and Sclerotinia sclerotium.

scholarly journals Synthesis, Spectral Characterization and Antimicrobial Evaluation of New Metal Complexes of Novel Schiff Base Derived from 4,6-dihydroxy-1,3-phenylenediethanone

2021 ◽  
Author(s):  
Yasmin mamdoh hussien Ahmed ◽  
Gehad G. Mohamed
Keyword(s):  
Staphylococcus Aureus ◽  
Schiff Base ◽  
Schiff Base Ligand ◽  
Magnetic Moment ◽  
Magnetic Measurements ◽  
Diffusion Method ◽  
Spectral Studies ◽  
Conductivity Measurements ◽  
Absorption Bands ◽  
Elemental Analyses

Abstract A new tetradentate Schiff base ligand was prepared from condensation of 4,6-dihydroxy-1,3-phenylenediethanone with ethane-1,2-diylbis(oxy)diethanamine. The ligand forms complexes in good yield. The Schiff base and its complexes were characterized by analytical (CHN elemental analyses, solubility, melting point, conductivity) measurements, spectral (IR, UV-vis, 1H NMR and MS) and magnetic measurements. The elemental analyses, Uv-vis spectra, and room temperature magnetic moment data and theoretically through density function theory were used as characterizing techniques in supporting of further interpretation of the complexes structures. The results of elemental analyses, EI-mass and conductivity measurements confirmed the stoichiometry of the ligand and its complexes while the characteristic absorption bands and resonance peaks in IR and NMR spectra confirmed the formation of the ligand frameworks around the metal ions. The octahedral environment for complexes derived from Schiff base ligand have been confirmed on the basis of results of electronic and diffused reflectance spectral studies and magnetic moment measurements. Detailed studies of the thermal properties of the Schiff base ligand and complexes were investigated by thermogravimetric technique. Moreover, the molecular docking into (PDB: 6NE0) was the DNA binding and supports the experimental finding and 6IY0 Crystal structure of conserved hypothetical protein SAV0927 from Staphylococcus aureus subsp. aureus Mu50. The synthesized ligand and its complexes were tested for in vitro antimicrobial activity against Candida albicans, Bacillus subtilis, Aspergillus flavus, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus by using agar-well diffusion method.

scholarly journals Ni(II) Dimers of NNO Donor Tridentate Reduced Schiff Base Ligands as Alkali Metal Ion Capturing Agents: Syntheses, Crystal Structures and Magnetic Properties

2018 ◽  
Vol 4 (4) ◽  
pp. 51 ◽  
Author(s):  
Monotosh Mondal ◽  
Maharudra Chakraborty ◽  
Michael G. B. Drew ◽  
Ashutosh Ghosh
Keyword(s):  
Schiff Base ◽  
Metal Ion ◽  
Magnetic Measurements ◽  
Dft Method ◽  
Distorted Octahedral Geometry ◽  
Schiff Base Ligands ◽  
Reduced Schiff Base ◽  
Ferromagnetic Interactions ◽  
Experimental Values ◽  
Reduced Schiff Base Ligands

Three trinuclear Ni(II)-Na(I) complexes,[Ni2(L1)2NaCl3(H2O)]·H2O (1), [Ni2(L2)2NaCl3(H2O)] (2), and [Ni2(L3)2NaCl3(OC4H10)] (3) have been synthesized using three different NNO donor tridentate reduced Schiff base ligands, HL1= 2-[(3-methylamino-propylamino)-methyl]-phenol, HL2= 2-[(3-methylamino-propylamino)-methyl]-4-chloro-phenol, and HL3= 2-[(3-methylamino-propylamino)-methyl]-6-methoxy-phenol that had been structurally characterized. Among these complexes, 1 and 2 are isostructural in which dinuclearNi(II) units act as metalloligands to bind Na(I) ions via phenoxido and chlorido bridges. The Na(I) atom is five-coordinated, and the Ni(II) atom possesses hexacordinated distorted octahedral geometry. In contrast, in complex 3, two -OMe groups from the dinuclear Ni(II) unit also coordinate to Na(I) to make its geometry heptacordinated pentagonal bipyramidal. The magnetic measurements of complexes 1–3 indicate ferromagnetic interactions between dimeric Ni(II) units with J = 3.97 cm−1, 4.66 cm−1, and 5.50 cm−1for 1–3, respectively, as is expected from their low phenoxido bridging angles (89.32°, 89.39°, and 87.32° for 1–3, respectively). The J values have been calculated by broken symmetry DFT method and found to be in good agreement with the experimental values.

scholarly journals Complexes of some 3d-metals with a Schiff base derived from 5-acetamido-1,3,4-thiadiazole-2-sulphonamide and their biological activity

2011 ◽  
Vol 76 (10) ◽  
pp. 1387-1394 ◽  
Author(s):  
Suman Malik ◽  
Suparna Ghosh ◽  
Liviu Mitu
Keyword(s):  
Schiff Base ◽  
Fungicidal Activity ◽  
Particle Size Analysis ◽  
Bidentate Ligand ◽  
Octahedral Geometry ◽  
Spectral Studies ◽  
Size Analysis ◽  
3D Metals ◽  
Complexes Of Transition Metals ◽  
The Stability

Using a bidentate ligand, a Schiff base of 5-acetamido-1,3,4- thiadiazole-2-sulphonamide, complexes of transition metals having the general formula ML2, where M = Mn(II), Fe(II), Ni(II) and Cu(II), were synthesized. The complexes were characterized by elemental analysis, molar conductivity, magnetic moment, electronic, ESR and IR spectroscopy, and particle size analysis. The conductivity data of the complexes suggests their non-electrolytic nature. The stability constants and free energy change for the complexes were calculated. Spectral studies and magnetic susceptibility measurements revealed an octahedral geometry for all the complexes. The ligand and its complexes were screened for their fungicidal activity against Aspergillus niger and A. flavus.

scholarly journals Antimicrobial and Antioxidant Activities of Diorganotin(IV) Complexes Synthesized from 1,2,4-Triazole Derivatives

2020 ◽  
Vol 32 (10) ◽  
pp. 2553-2558
Author(s):  
Jyoti Yadav ◽  
Jai Devi
Keyword(s):  
Schiff Base ◽  
Antioxidant Activities ◽  
Azomethine Nitrogen ◽  
Spectroscopic Techniques ◽  
Schiff Base Ligands ◽  
Alkyl Aryl ◽  
Aryl Group ◽  
Ft Ir ◽  
Tin Metal

Novel diorganotin(IV) complexes were synthesized from 1,2,4-triazole Schiff base ligands which were synthesized by reaction between the 4-amino-5-phenyl-1,2,4-triazole-3-thiol and salicyaldehyde derivatives. The bonding and geometry of the diorganotin(IV) complexes were evaluated by using different spectroscopic techniques such as FT-IR, mass, 1H, 13C & 119Sn NMR. The different spectroscopic techniques revealed the tridentate (ONS) mode of chelation of Schiff base ligands and pentacoordinated environment around the central tin metal which was satisfied with azomethine nitrogen, phenolic oxygen, thiolic sulfur and metal-carbon bond of alkyl/aryl group. The Schiff base ligands and their organotin(IV) complexes were tested for their in vitro antimicrobial and antioxidant activities to examine the biological outline of complexes in comparison to standard drugs. The results of activities data revealed that diorganotin(IV) complexes are more active than Schiff base ligands and some diorganotin(IV) complexes are even more active than the standard drugs. In all the synthesized complexes, compound 9 (Bu2SnL2) and 10 (Ph2SnL2) were most potent and can be used in future clinical trials.

scholarly journals Polydentate Schiff Base Ligands and Their La(III) Complexes: Synthesis, Characterization, Antibacterial, Thermal, and Electrochemical Properties

2012 ◽  
Vol 2012 ◽  
pp. 1-11 ◽  
Author(s):  
Ali E. Şabik ◽  
Muharrem Karabörk ◽  
Gökhan Ceyhan ◽  
Mehmet Tümer ◽  
Metin Dığrak
Keyword(s):  
Antimicrobial Activity ◽  
Schiff Base ◽  
Electrochemical Properties ◽  
Antimicrobial Activities ◽  
Nitrogen Atmosphere ◽  
Spectroscopic Methods ◽  
Schiff Base Ligands ◽  
One Step ◽  
The One ◽  
Reversible Transfer

We synthesized the Schiff base ligands H2L1–H2L4 and their La(III) complexes and characterized them by the analytical and spectroscopic methods. We investigated their electrochemical and antimicrobial activity properties. The electrochemical properties of the ligands H2L1–H2L4 and their La(III) complexes were studied at the different scan rates (100 and 200 mV), different pH ranges (), and in the different solvents. The electrooxidation of the Schiff base ligands involves a reversible transfer of two electrons and two protons in solutions of pH up to 5.5, in agreement with the one-step two-electron mechanism. In solutions of pH higher than 5.5, the process of electrooxidation reaction of the Schiff base ligands and their La(III) complexes follows an ECi mechanism. The antimicrobial activities of the ligands and their complexes were studied. The thermal properties of the metal complexes were studied under nitrogen atmosphere in the range of temperature 20–1000°C.

scholarly journals Synthesis and Structural Studies of Transition Metal Complexes with Bidentate Schiff Base Derived from 3-Acetyl-6-methyl-(2H)-pyran-2,4(3H)-dione

2011 ◽  
Vol 8 (s1) ◽  
pp. S245-S252 ◽  
Author(s):  
Praveen S. Mane ◽  
Sanjiv M. Salunke ◽  
Balagi S. More
Keyword(s):  
Schiff Base ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Octahedral Geometry ◽  
Ligand Field ◽  
Schiff Base Ligands ◽  
H Nmr ◽  
Dehydroacetic Acid ◽  
Ligand Field Parameters

The solid complexes of Cu(II), Ni(II), Co(II), Mn(II) and Fe(III) with Schiff base ligands derived from heterocyclic compounds 3-acetyl-6-methyl-(2H)-pyran-2,4(3H)-dione (Dehydroacetic acid) ando-chloroaniline were synthesized and characterized by elemental analysis, conductance, magnetic, thermal, UV-Vis and1H-NMR spectroscopy. The ligand field parameters have been evaluated for Cu(II), Ni(II), Co(II), Mn(II) and Fe(III) complexes which suggest an octahedral geometry for each of them. The magnetic moment and spectral data suggest the dimeric nature of Mn(II) complexes with octahedral geometry. The fungicidal activities of the ligands and their metal complexes have been screened in vitro againstAspergillus nigerand the percentage inhibition of the metal complexes is found to be increased considerably then that of their corresponding ligands and the order is Cu>Ni>Fe>Mn>Co.

Two New Copper (II) Complexes with the Same NNO Donor Schiff Base Ligand: A Monomer and a Dimer

2012 ◽  
Vol 67 (3) ◽  
pp. 192-196
Author(s):  
Bao Lin Liu ◽  
Yan Xia Wang ◽  
Ruo Jie Tao
Keyword(s):  
Experimental Data ◽  
Thermal Analysis ◽  
Schiff Base ◽  
Magnetic Measurements ◽  
Octahedral Geometry ◽  
Distorted Octahedral Geometry ◽  
Antiferromagnetic Exchange ◽  
X Ray ◽  
Distorted Octahedral ◽  
Best Fit

Two new copper(II) complexes, [(CuL)2(μ1,1-N3)2]・2H2O (1) and [Cu(HL)(2,2ʹ-bipy)- (CH3COO)]・ClO4・H2O (2), have been synthesized using the tridentate NNO Schiffbase ligand 2- [(2-aminoethylimino)methyl]-6-methoxyphenol (HL). They have been characterized by elemental analysis, IR spectroscopy, thermal analysis, and single-crystal X-ray analysis. The copper environment is distorted square pyramidal in complex 1: two nitrogen atoms and one oxygen atom from the ligands and two nitrogen atoms from two azido ligands build the coordination polyhedron around the copper atom. The Cu-Nazide-Cu angle in complex 1 is 85.6°. This is unusually small in comparison with the same angle in other end-on doubly azido-bridged dimers. Complex 2 is mononuclear with the Cu atom having a slightly distorted octahedral geometry. Magnetic measurements of 1 have been performed in the temperature range from 2 to 300 K. The experimental data indicate an antiferromagnetic exchange interaction between copper(II) ions bridged by the azido ligand. The best-fit parameters for complex 1 are g = 2.18 and J = −1.31 cm−1.

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