scholarly journals Synthesis, Spectroscopic and Electrochemical Studies of Mononuclear Fe(II) and Ni(II) Complexes Containing a Macrocyclic Ligand Derived from Pyridine-2,6-dicarboxaldehyde and 1,2-Bis(2-aminoethoxy) Ethane

2011 ◽  
Vol 3 (3) ◽  
pp. 599-607 ◽  
Author(s):  
M. M. Alam ◽  
R. Begum ◽  
S. M. M. Rahman ◽  
S. M. S. Islam

The cyclic (2+2) template condensation of 2,6-pyridinedicarboxaldehyde with 1,2-bis(2-aminoethoxy) ethane using Pb(SCN)2 as the metal source gave dinuclear lead(II) complex, Pb2L1(SCN)4 (1), where L1 is tetra-Schiff-base macrocycle. The transmetallation treatment of 1 with suitable metal perchlorate yield [FeL1](ClO4)2 (2) and [NiL1](ClO4)2 (3). The complexes (2 & 3) have been characterized by elemental analyses, IR, UV-visible, and ESI-MS spectroscopy. Based on spectral data, octahedral geometry may be proposed for these complexes. The electrochemical behavior of iron and nickel complexes is reported.Keywords:  Macrocyclic complexes; Spectroscopic studies; 1,2-Bis(2-aminoethoxy) ethane; Charge transfer.© 2011 JSR Publications. ISSN: 2070-0237 (Print); 2070-0245 (Online). All rights reserved.doi: 10.3329/jsr.v3i3.7231               J. Sci. Res. 3 (3), 609-617 (2011)

1998 ◽  
Vol 63 (3) ◽  
pp. 363-370 ◽  
Author(s):  
Violetta Patroniak-Krzyminiewska ◽  
Wanda Radecka-Paryzek

The template reactions of 2,6-diacetylpyridine with 3,6-dioxaoctane-1,8-diamine in the presence of dysprosium(III), thulium(III) and lutetium(III) chlorides and erbium(III) perchlorate produce the complexes of 15-membered macrocyclic ligand with an N3O2 set of donor atoms as a result of the [1+1] Schiff base cyclocondensation. In contrast, analogous reactions involving the lighter lanthanide ions (lanthanum(III), samarium(III) and europium(III)) yield the acyclic complexes with terminal acetylpyridyl groupings as products of the partial [2+1] condensation. The complexes were characterized by spectral data (IR, UV-VIS, 1H NMR, MS), and thermogravimetric and elemental analyses.


2006 ◽  
Vol 71 (5) ◽  
pp. 529-542 ◽  
Author(s):  
Kalagouda Gudasi ◽  
Siddappa Patil ◽  
Ramesh Vadavi ◽  
Rashmi Shenoy ◽  
Manjula Patil

A new macroacyclic amide ligand N,N?-bis(2-benzothiazolyl)-2,6-pyridinedicarboxamide (BPD), formed by the condensation of 2,6-pyridinedicarbonyldichloride with 2-aminobenzothiazole and its Cu(II), Ni(II), Co(II), Mn(II), Zn(II) and Cd(II) complexes were synthesized. Their structures were elucidated on the basis of elemental analyses, conductance measurements, magnetic moments, spectral (IR, NMR UV-Visible, EPR and FAB) and thermal studies. The complexes exhibit an octahedral geometry around the metal center. Conductance data of the complexes suggested them to be 1:1 electrolytes. The pentadentate behavior of the ligand was proposed on the basis of spectral studies. The X-band EPR spectra of the Cu(II) and Mn(II) complexes in the polycrystalline state at room (300 K) and liquid nitrogen temperature (77 K) were recorded and their salient features are reported.


2010 ◽  
Vol 7 (4) ◽  
pp. 1238-1245 ◽  
Author(s):  
Umendra Kumar ◽  
Sulekh Chandra

New cobalt(II) and nickel(II) complexes of 12-membered macrocyclic Schiff - base ligand containing thiosemicarbazone moiety as a part of ring have been prepared having general composition [MLX2] where M = Co(II) or Ni(II), L=3,4,9,10–tetra-2-furanyl-1,2,5,6,8,11- hexaazacyclododeca-7,12- dithione - 2,4,8,10 – tetraene, X = Cl-, NO3-, NCS-. The complexes have been characterized by elemental analysis, molar conductance, magnetic susceptibility measurements, spectral (IR, electronic, EPR) techniques and thermal analysis. Spectroscopic studies suggested a six coordinated octahedral geometry for all the complexes. The IR spectra of complexes suggest that ligand is coordinated to the metal ion through its four imines nitrogen. Conductivity measurements supported the non electrolytic nature of the complexes. The antifungal activities of complexes have been studied against a number of pathogenic fungi under laboratory conditions. The complexes showed good antifungal results. Thermal analysis of reported complexes suggests the absence of water molecule either in or outside the coordination sphere.


1978 ◽  
Vol 56 (15) ◽  
pp. 2000-2002 ◽  
Author(s):  
M. T. H. Tarafder ◽  
M. Akbar Ali

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.


2020 ◽  
Vol 10 (1) ◽  
pp. 1816-1824

Parent dioxomolybdenum(VI) complex formation by the reaction of MoO2(acac)2 with Schiff base tetradentate ligand, described in this paper. Schiff base tetradentate ligand [H2NCH2CH2 N=CC4H3S-CC4H3S=NCH2CH2NH2] obtained from the condensation of di-2-thienylethanedione with 1,2-diaminoethane. Macrocyclic molybdenum complexes were obtained from the cyclization of a synthesized complex with different 1,3 – diketones. The general formula of parent molybdenum complex is given as [MoO2( H2NCH2CH2 N=CC4H3S – CC4H3S=N CH2CH2NH2)](acac)2 and for macrocyclic molybdenum complex is [MoO2{(CH2CH2 N=CC4H3S – CC4H3S=N CH2CH2) N=C(R)CH2C(R’)=N}](acac)2. Ligand and all molybdenum complexes were characterized by elemental analyses(EA), molar conductivity(ΛM), ultraviolet(UV-Vis), and infrared (IR) spectral studies. The distorted octahedral geometry of element Mo in the parent as well as in macrocyclic molybdenum complexes is completed by two oxo O-atoms, four N-atoms from derived Schiff ligand.


2021 ◽  
Vol 20 (1) ◽  
pp. 113-117
Author(s):  
Amna Qasem Ali ◽  
Boubaker Hosouna ◽  
Khadija Abdusslam Ahmida ◽  
Abdulasalam Amhamed Mohamed Alshreef

Sulphur-nitrogen(SN) donor thiosemicarbazone ligand [(Z)-N-ethyl-2-(5-methyl-2-oxoindolin-3-ylidene)hydrazinecarbothioamide] and its Pt(II) complex were synthesized by condensation method. The compounds were structurally characterized by elemental analysis CHNS, FT-IR, and NMR analysis. The elemental analyses data for the compounds were in good agreement with the theoretical values.  The melting point of the complex was higher than the ligand, as expected. The FT-IR spectral data reflect a bidentate bonding of thiosemicarbazone ligand to Pt(II) ion through thioketo sulfur and azomethine nitrogen. The docking results (theoretical results) of these compounds show that the binding energy between DNA and Pt(II) complex was found to be less than that of the Schiff base ligand (L) in the sense that it has higher stability at various stages and angles. The strength of docking between DNA and Pt(II) complex was also found to be that stronger than the Schiff base ligand (L).


2018 ◽  
Vol 42 (4) ◽  
pp. 2952-2963 ◽  
Author(s):  
Ayşe İnan ◽  
Mesut İkiz ◽  
Seçil Erden Tayhan ◽  
Sema Bilgin ◽  
Nusret Genç ◽  
...  

A new series of ruthenium(ii) complexes 7–11 containing the –NN– group are synthesized and characterized via elemental analysis, and IR, UV-visible and 1H–13C NMR spectroscopy.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Gulsah Gumrukcu ◽  
Serkis Garikyan ◽  
Gulnur Keser Karaoglan ◽  
Dolunay Sakar

A new Schiff base with D-π-D type, (1E,2E)-3-[4-(dimethylamino)phenyl]prop-2-en-1-ylidene)phenylamine, has been successfully synthesized using the reaction of (2E)-3-[4-(dimethylamino)phenyl]acrylaldehyde with aniline. The Schiff base ligand has been characterized by FTIR, UV-visible, and1H NMR as well as TG/DTA, SEM, BET, and elemental analyses and mass spectra. Surface properties and acid-base constants of Schiff base ligand were determined by IGC measurements.


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