Synthesis of a novel, fluorescent, electroactive and metal ion sensitive thienylpyrrole derivate

2016 ◽  
Vol 40 (9) ◽  
pp. 8053-8059 ◽  
Author(s):  
Rukiye Ayranci ◽  
Metin Ak

A new novel, pyrene modified, thiophene–pyrrole based monomer was synthesized via a Schiff base reaction. It showed sensitive fluorescence changes when interacting with metal ions. Moreover, the electrochemical properties of its polymer were investigated.

2007 ◽  
Vol 72 (7) ◽  
pp. 908-916 ◽  
Author(s):  
Payman Hashemi ◽  
Hatam Hassanvand ◽  
Hossain Naeimi

Sorption and preconcentration of Cu2+, Zn2+ and Fe3+ on a salen-type Schiff base, 2,2'- [ethane-1,2-diylbis(nitrilomethylidyne)]bis(2-methylphenol), chemically immobilized on a highly crosslinked agarose support, were studied. Kinetic studies showed higher sorption rates of Cu2+ and Fe3+ in comparison with Zn2+. Half-times (t1/2) of 31, 106 and 58 s were obtained for sorption of Cu2+, Zn2+ and Fe3+ by the sorbent, respectively. Effects of pH, eluent concentration and volume, ionic strength, buffer concentration, sample volume and interferences on the recovery of the metal ions were investigated. A 5-ml portion of 0.4 M HCl solution was sufficient for quantitative elution of the metal ions from 0.5 ml of the sorbent packed in a 6.5 mm i.d. glass column. Quantitative recoveries were obtained in a pH range 5.5-6.5 for all the analytes. The volumes to be concentrated exceeding 500 ml, ionic strengths as high as 0.5 mol l-1, and acetate buffer concentrations up to 0.3 mol l-1 for Zn2+ and 0.4 mol l-1 for Cu2+ and Fe3+ did not have any significant effect on the recoveries. The system tolerated relatively high concentrations of diverse ions. Preconcentration factors up to 100 and detection limits of 0.31, 0.16 and 1.73 μg l-1 were obtained for Cu2+, Zn2+ and Fe3+, respectively, for their determination by a flame AAS instrument. The method was successfully applied to the metal ion determinations in several river water samples with good accuracy.


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


2021 ◽  
Vol 11 (4) ◽  
pp. 3989-4006

In the present research, a series of Ce+3 metal ions complexation with INZ incorporating Schiff bases have been reported. INZ incorporated Schiff Bases (3a-e) were developed by condensing INZ with substituted aromatic aldehyde and confirmed with various spectral Techniques such as Elemental analysis, UV, IR, 1H-NMR, 13H NMR. All the synthesized organic ligands were evaluated against antibacterial and antifungal stains and found moderate to significant results. The Ce+3 metal ion solution mixed with newly prepared bio-active INZ Schiff bases (3a-e) to afford the [Ce-INZ Schiff Base] complexes (4a-e). The stability constants of prepared complexes were evaluated and found in order as a (3e) > (3d) > (3a) > (3b) > (3c).


2013 ◽  
Vol 2013 ◽  
pp. 1-5
Author(s):  
Yeo Woon Yoon ◽  
Jong Seung Kim ◽  
Tae Hyun Kim

The electrochemical properties of an anthraquinone-containing Cu2+-promoted desulfurization chemodosimeter (AQCD) in the presence of various metal ions were investigated by voltammetry. AQCD showed voltammetric changes toward divalent metal ions (M2+), which are similar to those of anthraquinone (AQ) and 1-aminoanthraquinone (AQNH2) with the metal ions except Cu2+. This can be explained on the electrostatic interaction (AQCD-M2+) and chemodosimetric reaction (AQCD-Cu2+).


2010 ◽  
Vol 10 (3) ◽  
pp. 315-319 ◽  
Author(s):  
Ahmad Fatoni ◽  
Soerja Koesnarpadi ◽  
Nurlisa Hidayati

Synthesis, characterization and application of Diatomaceous Earth-4,4-Diamino diphenylether-O-Hydroxybenzaldehyde (diatomaceous earth-DDE-O-Hb) as an adsorbent of Ag(I) metal ion has been done. The aim of the purification of natural diatomaceous earth with KMnO4, H2SO4 and HCl were to obtain pure diatomaceous earth, remove the other compounds and de-alumination, respectively. The adsorbent of diatomaceous earth-DDE-O-Hb was synthesized by reacting pure diatomaceous earth with 3-chloropropyltrimethoxysilane, 4,4-diaminodiphenylether (DDE) and O-hydroxybenzaldehyde (O-Hb). The FTIR spectroscopy was used to identify Schiff base group in diatomaceous earth-DDE-O-Hb adsorbent. The diatomaceous earth-DDE-O-Hb was applied as adsorbent in the adsorption of Ag(I) metal ion. Parameters influencing the interaction such as time, pH and concentration were optimized. The result showed that diatomaceous earth-DDE-O-Hb adsorbent have Schiff base group. The interaction time of 90 min showed that 70.79% of Ag(I) metal ions at the concentration of 100 ppm can be adsorbed by diatomaceous earth-DDE-O-Hb adsorbent. At the pH solution between 2 to 7, the concentration of 100 ppm of Ag(I) metal ion that can adsorbed by diatomaceous earth-DDE-O-Hb adsorbent was up to 98% and at the concentration of 25 ppm Ag(I) metal ion, the adsorption of Ag(I) by diatomaceous earth-DDE-O-Hb adsorbent was near 91%.


2019 ◽  
Author(s):  
Chem Int

A study of removal of heavy metal ions from heavy metal contaminated water using agro-waste was carried out with Musa paradisiaca peels as test adsorbent. The study was carried by adding known quantities of lead (II) ions and cadmium (II) ions each and respectively into specific volume of water and adding specific dose of the test adsorbent into the heavy metal ion solution, and the mixture was agitated for a specific period of time and then the concentration of the metal ion remaining in the solution was determined with Perkin Elmer Atomic absorption spectrophotometer model 2380. The effect of contact time, initial adsorbate concentration, adsorbent dose, pH and temperature were considered. From the effect of contact time results equilibrium concentration was established at 60minutes. The percentage removal of these metal ions studied, were all above 90%. Adsorption and percentage removal of Pb2+ and Cd2+ from their aqueous solutions were affected by change in initial metal ion concentration, adsorbent dose pH and temperature. Adsorption isotherm studies confirmed the adsorption of the metal ions on the test adsorbent with good mathematical fits into Langmuir and Freundlich adsorption isotherms. Regression correlation (R2) values of the isotherm plots are all positive (>0.9), which suggests too, that the adsorption fitted into the isotherms considered.


2018 ◽  
Vol 69 (7) ◽  
pp. 1678-1681
Author(s):  
Amina Mumtaz ◽  
Tariq Mahmud ◽  
M. R. J. Elsegood ◽  
G. W. Weaver

New series of copper (II), cobalt (II), zinc (II), nickel (II), manganese (II), iron (II) complexes of a novel Schiff base were prepared by the condensation of sulphadizine and pyridoxal hydrochloride. The ligand and metal complexes were characterized by utilizing different instrumental procedures like microanalysis, thermogravimetric examination and spectroscopy. The integrated ligand and transition metal complexes were screened against various bacteria and fungus. The studies demonstrated the enhanced activity of metal complexes against reported microbes when compared with free ligand.


2019 ◽  
Vol 9 (2) ◽  
pp. 151-162
Author(s):  
Shveta Acharya ◽  
Arun Kumar Sharma

Background: The metal ions play a vital role in a large number of widely differing biological processes. Some of these processes are quite specific in their metal ion requirements. In that only certain metal ions, in specific oxidation states, can full fill the necessary catalytic or structural requirement, while other processes are much less specific. Objective: In this paper we report the binding of Mn (II), Ni (II) and Co (II) with albumin are reported employing spectrophotometric and pH metric method. In order to distinguish between ionic and colloidal linking, the binding of metal by using pH metric and viscometric methods and the result are discussed in terms of electrovalent and coordinate bonding. Methods: The binding of Ni+2, Co+2 and Mn+2 ions have been studied with egg protein at different pH values and temperatures by the spectrometric technique. Results: The binding data were found to be pH and temperature dependent. The intrinsic association constants (k) and the number of binding sites (n) were calculated from Scatchard plots and found to be at the maximum at lower pH and at lower temperatures. Therefore, a lower temperature and lower pH offered more sites in the protein molecule for interaction with these metal ions. Statistical effects seem to be more significant at lower Ni+2, Co+2 and Mn+2 ions concentrations, while at higher concentrations electrostatic effects and heterogeneity of sites are more significant. Conclusion: The pH metric as well as viscometric data provided sufficient evidence about the linking of cobalt, nickel and manganese ions with the nitrogen groups of albumin. From the nature and height of curves in the three cases it may be concluded that nickel ions bound strongly while the cobalt ions bound weakly.


Sign in / Sign up

Export Citation Format

Share Document