scholarly journals Syntheses, Magnetic and Spectral Studies on the Coordination Compounds of the Polystyrene-anchored Thiazolidin-4-one

2012 ◽  
Vol 9 (4) ◽  
pp. 2532-2539 ◽  
Author(s):  
Dinesh Kumar ◽  
Amit Kumar
Keyword(s):  
Coordination Compounds ◽  
Acid Hydrazide ◽  
Mercaptoacetic Acid ◽  
Spectral Studies ◽  
Donor Ligand ◽  
Square Planar ◽  
Elemental Analyses ◽  
Ir Reflectance ◽  
Bipyramidal Structure ◽  
Monodentate Ligands

The reaction between polystyrene 3-formylsalicylate and thiophene-2-carboxylic acid hydrazide in DMF in the presence of ethyl acetate results in the formation of polystyrene N-(2-carbamoylthienyl)-3'-carboxy-2'-hydroxybenzylideneimine (I). A benzene suspension of I reacts with mercaptoacetic acid and forms the polystyrene N-(2-carbamoylthienyl)-C-(3'-carboxy-2'-hydroxyphenyl) thiazolidin-4-one, PSCH2–LH2(II). A DMF suspension of II reacts with Zn(II), Co(II), Cu(II), Zr(OH)2(IV) and MoO2(VI) ions and forms the corresponding polystyrene-anchored coordination compounds, [PSCH2–LZn(DMF)] (III), [PSCH2–LCo(DMF)3] (IV), [PSCH2–LHCu(OAc)] (V), [PSCH2–LH2Zr(OH)2(OAc)2] (VI) and [PSCH2–LHMoO2(acac)] (VII) respectively. The polystyrene-anchored coordination compounds have been characterized on the basis of elemental analyses, spectral (IR, reflectance, ESR) studies and magnetic susceptibility measurements. II acts as a neutral tridentate ONS donor ligand in VI, a monobasic bidentate OS donor ligand in VII, a monobasic tridentate ONS donor ligand in V and a dibasic tridentate ONO donor ligand in III and IV. The acetato groups behave as monodentate ligands in V and VI. A square-planar structure for V, a tetrahedral structure for III, an octahedral structure for IV and VII and a pentagonal-bipyramidal structure for VI are suggested.

scholarly journals Physico-Chemical Studies on the Coordination Compounds of Thiazolidin-4-One

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Dinesh Kumar ◽  
Amit Kumar ◽  
Jyoti Sharma
Keyword(s):  
Coordination Compounds ◽  
Benzene Solution ◽  
Molar Conductance ◽  
Mercaptoacetic Acid ◽  
Donor Ligand ◽  
Physico Chemical ◽  
Square Planar ◽  
Elemental Analyses ◽  
Ir Reflectance ◽  
Chemical Studies

A dry benzene solution of the Schiff base,N-(2-hydroxyphenyl)-3′-carboxy-2′-hydroxybenzylideneimine upon reacting with mercaptoacetic acid undergoes cyclization and formsN-(2-hydroxyphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one, LH3(I). A MeOH solution ofIreacts with , , , and Mo ions and forms the monomeric coordination compounds, [Mn(LH)(MeOH)3] (II), [Cu(LH)(MeOH)] (III), [Zn(LH)(MeOH)] (IV), [FeCl(LH)(MeOH)2] (V), and [MoO2(LH)(MeOH)](VI). The coordination compounds have been characterized on the basis of elemental analyses, molar conductance, molecular weight, spectral (IR, reflectance, ESR) studies, and magnetic susceptibility measurements.Ibehaves as a dibasic tridentate OOS donor ligand in these compounds. The compounds are nonelectrolytes ( = 6.2–13.8 mho cm2 mol−1) in DMF. A square-planar structure forIII; a tetrahedral structure forIVand an octahedral structure forII,V, andVIare suggested.

scholarly journals Syntheses, Magnetic, Spectral and Biological Studies on the Coordination Compounds of N-(2-Hydroxyphenyl)-C-(3′- Carboxy-2′-Hydroxyphenyl) Thiazolidin-4-One

2021 ◽  
Vol 23 (08) ◽  
pp. 135-142
Author(s):  
Praveen Kumar Gupta ◽  
◽  
Amit Kumar ◽  
Dinesh Kumar ◽  
◽  
...  
Keyword(s):  
Coordination Compounds ◽  
Benzene Solution ◽  
Antibacterial Activities ◽  
Molar Conductance ◽  
Mercaptoacetic Acid ◽  
Donor Ligand ◽  
Gram Positive Bacteria ◽  
Biological Studies ◽  
Elemental Analyses ◽  
Ir Reflectance

A dry benzene solution of the Schiff base, N-(2-hydroxyphenyl)-3′-carboxy-2′- hydroxybenzylideneimine upon reacting with mercaptoacetic acid undergoes cyclization and forms N- (2-hydroxyphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one, LH3 (I). A MeOH solution of I reacts with Ni(II) and UO2(VI) ions and forms the monomeric coordination compounds, [Ni(LH)(MeOH)3] and [UO2(LH)(MeOH)]. The coordination compounds have been characterized on the basis of elemental analyses, molar conductance, molecular weight, spectral (IR, reflectance) studies and magnetic susceptibility measurements. I behaves as a dibasic tridentate OOS donor ligand in these compounds. The compounds are non-electrolytes (M = 4.3-6.4 mho cm2 mol-1) in DMF. Octahedral structure for Ni(II) and UO2(VI) compounds are suggested. LH3 (I) and its complexes while testing with E.Coli. (Gram Negative) and S. Aureus (Gram positive) bacteria show antibacterial activities.

scholarly journals Physicochemical, Spectral, and Biological Studies of Mn(II), Cu(II), Cd(II), Zr(OH)2(IV), and UO2(VI) Compounds with Ligand Containing Thiazolidin-4-one Moiety

2014 ◽  
Vol 2014 ◽  
pp. 1-9
Author(s):  
Dinesh Kumar ◽  
Amit Kumar
Keyword(s):  
Antibacterial Activities ◽  
Molar Conductance ◽  
Mercaptoacetic Acid ◽  
Coordinate Structure ◽  
Donor Ligand ◽  
E Coli ◽  
Biological Studies ◽  
Elemental Analyses ◽  
Ir Reflectance ◽  
Bipyramidal Structure

The Schiff base (I) upon reacting with mercaptoacetic acid in dry benzene undergoes cyclization and forms N-(2-carbamoylthienyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one, LH3(II). A MeOH solution ofIIreacts with Mn(II), Cu(II), Cd(II), Zr(OH)2(IV), and UO2(VI) ions and forms the coordination compounds, [Mn(LH)(MeOH)2], [Cu(LH)]2, [Cd(LH)], [Zr(OH)2(OAc)2(LH3)], and [UO2(NO3)(LH2)(MeOH)]. The compounds have been characterized on the basis of elemental analyses, molar conductance, molecular weight, spectral (IR, reflectance, and EPR) studies and magnetic susceptibility measurements. LH3behaves as a neutral tridentate ONS donor ligand in [Zr(OH)2(OAc)2(LH3)], monobasic tridentate ONS donor ligand in [UO2(NO3)(LH2)(MeOH)], dibasic tridentate OOS donor ligand in [Cu(LH)]2and dibasic tetradentate OONO donor ligand in [Mn(LH)(MeOH)2] and [Cd(LH)]. [Cu(LH)]2is dimer, while all other compounds are monomers in diphenyl. A square-planar structure for [Cu(LH)]2, a tetrahedral structure for [Cd(LH)], an octahedral structure for [Mn(LH)(MeOH)2], a pentagonal-bipyramidal structure for [Zr(OH)2(OAc)2(LH3)], and an eight-coordinate structure for [UO2(NO3)(LH2)(MeOH)] are proposed. The ligand (II) and its compounds show antibacterial activities towardsE. coli. (Gram negative) andS. aureus(Gram positive).

scholarly journals Syntheses, Spectral Characterization, and Antimicrobial Studies on the Coordination Compounds of Metal Ions with Schiff Base Containing Both Aliphatic and Aromatic Hydrazide Moieties

2013 ◽  
Vol 2013 ◽  
pp. 1-10 ◽  
Author(s):  
Dinesh Kumar ◽  
Silky Chadda ◽  
Jyoti Sharma ◽  
Parveen Surain
Keyword(s):  
Schiff Base ◽  
Coordination Compounds ◽  
Molar Conductance ◽  
Equimolar Ratio ◽  
Gram Positive Bacteria ◽  
H Nmr ◽  
Antimicrobial Studies ◽  
Elemental Analyses ◽  
Ir Reflectance ◽  
Bipyramidal Structure

An EtOH solution of 3-ketobutanehydrazide and salicylhydrazide on refluxing in equimolar ratio forms the corresponding Schiff base, LH3(1). The latter reacts with Mn(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II), Zr(OH)2(IV), MoO2(VI), and UO2(VI) ions in equimolar ratio and forms the corresponding coordination compounds, [M(LH)(MeOH)3] (2, M = Mn, Co, Ni), [Cu(LH)]2(3), [M′(LH)(MeOH)] (4, M′ = Zn, Cd), [Zr(OH)2(LH)(MeOH)2] (5), [MoO2(LH)(MeOH)] (6), and [UO2(LH)(MeOH)] (7). The coordination compounds have been characterized on the basis of elemental analyses, molar conductance, spectral (IR, reflectance,1H NMR, ESR) studies, and magnetic susceptibility measurements. They are nonelectrolytes in DMSO. The coordination compounds, except3, are monomers in diphenyl. They are active against gram-positive bacteria (S. aureus, B. subtilis), gram-negative bacteria (E. coli, P. aeruginosa), and yeast (S. cerevisiae, C. albicans).1acts as a dibasic tridentate ONO donor ligand in2–7coordinating through its both enolic O and azomethine N atoms. The coordination compounds2and3are paramagnetic, while rest of the compounds are diamagnetic. A square-planar structure to3, a tetrahedral structure to4, an octahedral structure to2,6, and7, and a pentagonal bipyramidal structure to5are proposed.

scholarly journals Immobilised nickel(II), dioxomolybdenum(VI) and dioxouranium(VI) complexes on polystyrene resin

2021 ◽  
Vol 23 (06) ◽  
pp. 11201-1127
Author(s):  
Amit Kumar ◽  
◽  
Praveen Kumar Gupta ◽  
Sunil Kumar ◽  
Dinesh Kumar ◽  
...  
Keyword(s):  
Magnetic Susceptibility ◽  
Schiff Bases ◽  
Coordination Compounds ◽  
Metal Salt ◽  
Donor Behavior ◽  
Square Planar ◽  
Elemental Analyses ◽  
Ir Reflectance ◽  
Polystyrene Resin ◽  
Supported Ni

New polystyrene supported mixed Schiff bases(PSCH 2 –LH 2 ) and their coordination compounds with nickel(II), dioxomolybdenum(VI), and dioxouranium(VI) have been synthesized. PSCH 2 –LH 2 have been synthesized by the reaction of chloromethylated polystyrene crosslinked with divinylbenzene(PSCH 2 –Cl) and the Schiff bases(LH 2 ) derived from 3-formylsalicylic acid, ethylenediamine or propylene diamine, and acetylacetone. The polystyrene-supported coordination compounds are of the types: PSCH 2 –LM(where M = Ni, MoO 2, UO 2 ). They have been synthesized by the reaction of PSCH 2 –LH 2 and the metal salt/metal coordination compounds in DMF. The coordination compounds have been characterized on the basis of elemental analyses, IR, reflectance, and magnetic susceptibility measurements. The shifts of the ν (C=N)(azomethine), ν (C–O)(phenolic) and ν (C–O)(enolic) stretches indicate the ONNO donor behavior of PSCH 2 –LH 2. The polystyrene-supported Ni(II) compound is square planar; MoO2 (VI) and UO2 (VI) compounds are octahedral and Zr(IV) compounds are pentagonal bipyramidal. The compounds, PSCH 2 –LM(where M = Ni, MoO 2, and UO 2 ) are diamagnetic.

scholarly journals Syntheses and Characterization of the Coordination Compounds of N-(2-hydroxymethylphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Dinesh Kumar ◽  
Amit Kumar ◽  
Durga Dass
Keyword(s):  
Molecular Weight ◽  
Coordination Compounds ◽  
Benzene Solution ◽  
Molar Conductance ◽  
Mercaptoacetic Acid ◽  
Octahedral Structure ◽  
Donor Ligand ◽  
Tetrahedral Structure ◽  
Elemental Analyses

A dry benzene solution of the Schiff base N-(2-hydroxymethylphenyl)-3′-carboxy-2′-hydroxybenzylideneimine upon reacting with mercaptoacetic acid undergoes cyclization and forms N-(2-hydroxymethylphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidin-4-one, LH3 (I). A MeOH solution of I reacts with Co(II), Ni(II), Cd(II), Zr(OH)2(IV), and UO2(VI) ions and forms the monomeric coordination compounds, [M(LH)(MeOH)3] [where M = Co(II), Ni(II)], [M′(LH)(MeOH)] [here M′ = Cd(II), UO2(VI)] and [Zr(OH)2(LH)(MeOH)]. The coordination compounds have been characterized on the bases of elemental analyses, molar conductance, molecular weight, spectral (IR, NMR, and reflectance) studies, and magnetic susceptibility measurements. I behaves as a dibasic tridentate OOS donor ligand in these compounds. The compounds are nonelectrolytes (ΛM = 3.8–8.9 mho cm2 mol−1) in DMF. A tetrahedral structure for [Cd(LH)(MeOH)] and an octahedral structure for the remaining compounds are suggested.

scholarly journals Preparation and Spectroscopic Characterization of Polymer-Supported Transition Metal Complexes

2019 ◽  
Vol 31 (9) ◽  
pp. 2087-2090
Author(s):  
P.K. Gupta ◽  
Dinesh Kumar ◽  
Amit Kumar
Keyword(s):  
Schiff Base ◽  
Coordination Compounds ◽  
Metal Salt ◽  
Spectroscopic Characterization ◽  
Square Planar ◽  
Elemental Analyses ◽  
Ir Reflectance ◽  
Donor Behaviour ◽  
Solvent Molecules

Novel polystyrene supported mixed Schiff base (PSCH2–LH2) and its coordination compounds with copper(II) and zirconium(IV) have been synthesized. PSCH2–LH2 has been synthesized by the reaction of chloromethylated polystyrene crosslinked with divinylbenzene (PSCH2–Cl) and the Schiff base (LH2) derived from 3-formylsalicylic acid, propylenediamine and acetylacetone. The polystyrene supported coordination compounds are of the types: [PSCH2–LCu] and [PSCH2–LZr(OH)2·DMF]. They have been synthesized by the reaction of PSCH2–LH2 and the metal salt in DMF. The coordination compounds have been characterized on the basis of elemental analyses, IR, reflectance, ESR spectral and magnetic susceptibility measurements. The shifts of the ν(C=N) (azomethine), ν(C–O) (phenolic) and ν(C–O) (enolic) stretches indicate the ONNO donor behaviour of PSCH2–LH2. The polystyrene supported Cu(II) compound is square planar and Zr(IV) compound is pentagonal bipyramidal. The coordinated solvent molecules are completely lost from metal bound coordination compound by heating them at definite temperature in an air oven for 3 h. The compound, PSCH2–LCu is paramagnetic, while PSCH2–LZr(OH)2·DMF is diamagnetic.

scholarly journals Synthesis, Structural, and Antimicrobial Studies of Some New Coordination Compounds of Palladium(II) with Azomethines Derived from Amino Acids

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Monika Gupta ◽  
Sangeeta Sihag ◽  
A. K. Varshney ◽  
S. Varshney
Keyword(s):  
Amino Acids ◽  
Coordination Compounds ◽  
Reaction Medium ◽  
Molar Ratio ◽  
Spectral Studies ◽  
Antimicrobial Studies ◽  
Elemental Analyses ◽  
C Nmr ◽  
Insecticidal Activities

Some new coordination compounds of palladium(II) have been synthesized by the reaction of palladium(II) acetate with azomethines in a 1 : 2 molar ratio using acetonitrile as a reaction medium. Azomethines used in these studies have been prepared by the condensation of 2-acetyl fluorene and 4-acetyl biphenyl with glycine, alanine, valine, and leucine in methanol. An attempt has been made to probe their bonding and structures on the basis of elemental analyses and IR,1H, and13C NMR spectral studies. Pd(II) compounds have been found to be more active than their uncomplexed ligands as both of them were screened for antibacterial, antifungal, and insecticidal activities.

Chelates of nickel(II) and copper(II) with tridentate Schiff base formed by the condensation of S-benzyldithiocarbazate with benzoin

1978 ◽  
Vol 56 (15) ◽  
pp. 2000-2002 ◽  
Author(s):  
M. T. H. Tarafder ◽  
M. Akbar Ali
Keyword(s):  
Schiff Base ◽  
Spectral Data ◽  
General Formula ◽  
Schiff Base Ligand ◽  
Nickel Complexes ◽  
Planar Structure ◽  
Spectral Studies ◽  
Square Planar ◽  
Elemental Analyses ◽  
Tridentate Schiff Base

New complexes with the Schiff base ligand derived from S-benzyldithiocarbazate (NH2—NH—CSSCH2C6H5) have been prepared and characterized by elemental analyses, magnetic, conductometric, ir, and electronic spectral studies. The tridentate ONS Schiff base S-benzyl-β-N-(phenyl, phenylhydroxymethyl)methylenedithiocarbazate gave mono-ligand complexes with Ni(II) and Cu(II) having the general formula [MligandX] (M = Ni(II) and Cu(II); X = NO3, Cl, Br, NCS). A proposed square-planar structure for the nickel complexes is supported by magnetic and spectral data. A square-planar structure is also suggested for Cu(II) complexes. The ir results give evidence of the different bondings present in the complexes.

scholarly journals Syntheses, Characterization, and Biological Activities of Metal Complexes of N-(2-Carbamoylthienyl)-C-(3′-carboxy-2′-hydroxyphenyl) Azetidin-2-one with Some Di-, Tetra-, and Hexavalent Metal Ions

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Dinesh Kumar ◽  
Amit Kumar
Keyword(s):  
Coordination Compounds ◽  
Biological Activities ◽  
Antibacterial Activities ◽  
Molar Conductance ◽  
Octahedral Structure ◽  
Coordinate Structure ◽  
Donor Ligand ◽  
E Coli ◽  
Elemental Analyses ◽  
Subnormal Magnetic Moment

The cyclization of the Schiff base, N-(2-carbamoylthienyl)-3′-carboxy-2′-hydroxybenzylideneimine with ClCH2COCl in dioxane, in the presence of triethylamine (Et3N) forms N-(2-carbamoylthienyl)-C-(3′-carboxy-2′-hydroxyphenyl) azetidin-2-one, LH3(I). A methanolic solution ofIreacts with Co(II), Cu(II), Zn(II), Zr(OH)2(IV), and MoO2(VI) ions and forms the coordination compounds, [Co(LH)(MeOH)]2(II), [Cu(LH)]2(III), [Zn(LH)(MeOH)2] (IV), [Zr(OH)2(LH)(MeOH)] (V), and [MoO2(LH)(MeOH)2] (VI). The compounds have been characterized on the basis of elemental analyses, molar conductance, molecular weight, spectral (IR, NMR, reflectance, and ESR) studies, and magnetic susceptibility measurements. All the coordination compounds are nonelectrolytes (ΛM=3.1-9.2 mho cm2mol−1) in DMF.Ibehaves as a dibasic tridentate OON donor ligand inV; a dibasic tetradentate OONO donor ligand inII,III, andVI; and a dibasic tetradentate OONS donor ligand inIV.IIandIIIare dimers, while others are monomers in diphenyl.IIIexhibits subnormal magnetic moment (1.55 B.M.) and is involved in antiferromagnetic exchange, while the other complexes are magnetically dilute. A square-pyramidal structure forIIIand an octahedral structure forII,IV, andVare suggested.VIexhibits an eight-coordinate structure. The ligand (I) and its compounds show antibacterial activities towardsE. coli(gram negative) andS. aureus(gram positive).

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