Synthesis, Characterization and Emission Properties of a Mixed Metal Complex of Europium (III) and Terbium (III) with a Tripodal Heptadentate Schiff Base Ligand

2012 ◽  
Vol 463-464 ◽  
pp. 326-330
Author(s):  
Masatoshi Kanesato ◽  
Keiko Nagahara ◽  
Midori Goto

The preparation and characterization of a novel mixed metal complex of europium (III) and terbium (III) of a tripodal heptadentate Schiff-base ligand N [CH2CH2N=CH (2-OH-3-MeC6H3)]3 (H3L1) have been studied. The complex was prepared by the reaction of [EuL1] and [TbL1] in N, N-dimethylformamide. The ratio of europium (III) to terbium (III) in the mixed metal complex was found to be 3 to 7. The molecular structure of [Eu0.3Tb0.7L1] was determined by X-ray crystallography. The crystal structure analysis revealed that the Schiff-base behaves as a tri-deprotonated heptadentate ligand encapsulating the each metal ion within the N4O3 cavity. Under the excitation of UV light, the solid state of the complex exhibited red emission corresponding to europium (III) ion. The emission bands of 5D0 → 7Fj (j = 2, 3, 4) were observed at 609, 652, and 706 nm, respectively. On the other hand, the green emission corresponding to terbium (III) ion was not observed.

Author(s):  
Shabana Noor ◽  
Richard Goddard ◽  
Fehmeeda Khatoon ◽  
Sarvendra Kumar ◽  
Rüdiger W. Seidel

AbstractSynthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes with the formula [ZnLn(HL)(µ-OAc)(NO3)2(H2O)x(MeOH)1-x]NO3 · n H2O · n MeOH [Ln = Pr (1), Nd (2)] and the crystal and molecular structure of [ZnNd(HL)(µ-OAc)(NO3)2(H2O)] [ZnNd(HL)(OAc)(NO3)2(H2O)](NO3)2 · n H2O · n MeOH (3) are reported. The asymmetrical compartmental ligand (E)-2-(1-(2-((2-hydroxy-3-methoxybenzylidene)amino)-ethyl)imidazolidin-2-yl)-6-methoxyphenol (H2L) is formed from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation, resulting in a peripheral imidazoline ring. The structures of 1–3 were revealed by X-ray crystallography. The smaller ZnII ion occupies the inner N2O2 compartment of the ligand, whereas the larger and more oxophilic LnIII ions are found in the outer O2O2’ site. Graphic Abstract Synthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes (Ln = Pr, Nd) bearing an asymmetrical compartmental ligand formed in situ from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation are reported.


2012 ◽  
Vol 9 (4) ◽  
pp. 2119-2127 ◽  
Author(s):  
Gajendra Kumar ◽  
Rajeev Johari ◽  
Shoma Devi

A Schiff base ligand was synthesized by reacting 5-tert-butl-2-hydroxy-3-(3-phenylpent-3-yl) benzaldehyde and thiodihydrazide (2:1) and a series of metal complexes with this new ligand were synthesized by reaction with Cr (III), Mn (III), and Fe (III) metal salt in methanolic medium. The Schiff base ligand and its complexes have been characterized with the help of elemental analysis, conductance measurements, magnetic measurements and their structure configuration have been determined by various spectroscopic (electronic, IR,1H NMR,13C NMR, GCMS) techniques. Electronic and magnetic moments of the complexes indicate that the geometries of the metal centers were octahedral. IR spectral data suggest that ligand behaves as a tetradentate ligand with ONNO donor sequence towards the metal ion.


2014 ◽  
Vol 2014 ◽  
pp. 1-11 ◽  
Author(s):  
Shabnum Bashir ◽  
Syed Raashid Maqsood ◽  
Ghulam Mustafa Peerzada ◽  
Badruddin Khan ◽  
Masood Ahmad Rizvi

We report the comparative synthetic methodologies and characterization of a tetradentate Schiff base ligand 1,2-(diimino-4′-antipyrinyl)-1,2-diphenylethane (DE). The target synthesis of oxovanadium(IV) and dioxouranium(VI) complexes (vanadyl and uranyl) with the (DE) ligand was also attempted to envisage the effect of metal ion steric factor on complexation process through solution phase thermodynamic and kinetic studies. The thermodynamic stabilities of synthesized vanadyl and uranyl (DE) complexes are discussed in light of their solution phase thermodynamic stability constants obtained by electroanalytical method. A comparative kinetic profile of vanadyl and uranyl complexation with DE is also reported. The complexation reaction proceeds with an overall 2nd order kinetics with both metal ions. Temperature dependent studies of rate constants present an activation energy barrier of ca. 40.913 and 48.661 KJ mol−1, for vanadyl and uranyl complexation, respectively, highlighting the metal ion steric and ligand preorganization effects. The synthesized Schiff base ligand and its vanadyl and uranyl complexes were screened for biocidal potential as antibacterial, antifungal, and anthelmintic agents with the results compared to corresponding reference drugs.


2012 ◽  
Vol 9 (1) ◽  
pp. 55-59
Author(s):  
Shahriar Ghammamy ◽  
Sajjad Sedaghat

We describe the synthesis and characterization of a new Co(III) complex of the Schiff base ligand (N1 E, N2E) - N1-((1H- pyrrol-2-yl) methylene) - N2-(1- phenylethylidene) ethane- 1,2- diamineabbreviated as MPEAwas synthesized and characterized.Co (III) Metal complex of this Schiff base ligand prepared by reaction of CoCl2.6H2O with MPEA. Characterization of the ligand was made by microanalyses, FT-IR, 1HNMR and 13CNMR and its complex was made by FT-IR.


2019 ◽  
Vol 1181 ◽  
pp. 536-545 ◽  
Author(s):  
Rania H. Taha ◽  
Zienab A. El-Shafiey ◽  
Aida A. Salman ◽  
Esmail M. El-Fakharany ◽  
Mai M. Mansour

2018 ◽  
Vol 4 (4) ◽  
pp. 151-162
Author(s):  
Dasari Ayodhya ◽  
Guttena Veerabhadram

We report the simple synthesis of zinc sulfide nanoparticles (ZnSNPs) by a co-precipitation method using Schiff base, (2-[(4-methoxy-phenylimino)-methyl]-4-nitro phenol) as a capping agent. Here, Schiff base is also used as N, O-donor ligand to control the morphology of NPs and fluorescence interactions. The formation of ZnSNPs and their optical, structural, thermal properties and morphologies were studied by means of UV–vis DRS, fluorescence, FTIR, XRD, SEM, TEM, zeta potential and TGA. The optical properties and quantum confinement effect of the products were confirmed by means of spectroscopic measurements. XRD and TEM image shows that the synthesized ZnSNPs have cubic structures with a diameter of about less than 10 nm. The prepared ZnSNPs exhibited as a selective probe detection of Fe3+, Cr2+ and Cd2+ ions by fluorometrically and the emission band which disappears in the presence of increasing concentrations of Fe3+, Cr2+ and Cd2+ ions. Based on the fluorescence quenching of the NPs in the presence of metal ion of interest, the feasibility of their determinations was examined according to the Stern-Volmer equation. Our work suggested that Schiff base capped ZnSNPs could be a potential selective sensor in the detection of heavy metal ions.


2017 ◽  
Vol 14 (1) ◽  
pp. 135-147
Author(s):  
Baghdad Science Journal

The free Schiff base ligand (HL1) is prepared by being mixed with the co-ligand 1, 10-phenanthroline (L2). The product then is reacted with metal ions: (Cr+3, Fe+3, Co+2, Ni+2, Cu+2 and Cd+2) to get new metal ion complexes. The ligand is prepared and its metal ion complexes are characterized by physic-chemical spectroscopic techniques such as: FT-IR, UV-Vis, spectra, mass spectrometer, molar conductivity, magnetic moment, metal content, chloride content and microanalysis (C.H.N) techniques. The results show the formation of the free Schiff base ligand (HL1). The fragments of the prepared free Schiff base ligand are identified by the mass spectrometer technique. All the analysis of ligand and its metal complexes are in good agreement with the theoretical values indicating the purity of Schiff base ligand and the metal complexes. From the above data, the molecular structures for all the metal complexes are proposed to be octahedral


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