Conductivity Studies of Schiff Base Ligands Derived from O-Phenylenediamine and Their Co(II) and Zn(II) Complexes

2015 ◽  
Vol 12 (2) ◽  
pp. 13
Author(s):  
Muhamad Faridz Osman ◽  
Karimah Kassim

The coordination complexes of Co(II) and Zn(II) with Schiff bases derived from o-pheny/enediamine and substituted 2-hydroxybenza/dehyde were prepared All compounds were characterized by Fourier transform infrared (FTIR) spectroscopy and Nuclear magnetic resonance (NMR.) spectroscopy elemental analyzers. They were analyzed using impedance spectroscopy in the frequency range of 100 Hz - 1 MHz. L1 and L2 showed higher conductivity compared to their metal complexes, which had values of 1.3 7 x 10-7 and 6.13 x 10-8 S/cm respectively.

2015 ◽  
Vol 12 (2) ◽  
pp. 13
Author(s):  
Muhamad Faridz Osman ◽  
Karimah Kassim

The coordination complexes of Co(II) and Zn(II) with Schiff bases derived from o-phenylenediamine and substituted 2-hydroxybenzaldehyde were prepared All compounds were characterized by Fourier transform infrared (FTIR) spectroscopy and Nuclear magnetic resonance (NMR) spectroscopy elemental analyzers. They were analyzed using impedance spectroscopy in the frequency range of 100Hz-1 MHz. LI and L2 showed higher conductivity compared to their metal complexes, which had values of 1.3 7 x 10-7 and 6.13 x 10-8 S/cm respectively. 


Clay Minerals ◽  
1986 ◽  
Vol 21 (5) ◽  
pp. 879-897 ◽  
Author(s):  
M. A. Wilson ◽  
S. A. McCarthy ◽  
P. M. Fredericks

AbstractThe structure of synthetic aluminosilicates prepared at pH 6 has been investigated by 29Si and 27Al high-resolution solid-state nuclear magnetic resonance (NMR) spectroscopy. Fourier transform infrared (FTIR) spectroscopy and electron microscopy have also been used to characterize the products. The amount of Si and Al in protoimogolite, disordered allophane and other structures has been measured. There is a fair correlation between the intensity of the 349 cm−1 band in the FTIR spectra and the proportion by weight of protoimogolite Si measured by NMR. It is shown that disordered allophanes have similar structures to those proposed by van Reeuwijk and de Villiers (Soil Sci. Soc. Am. Proc. 32 (1968) 238–240), i.e. octahedral Al surrounding a tetrahedral core. Moreover, it is clear that at high Al:Si ratios (⩾1:1), protoimogolite can compete with disordered allophane precursors for aluminum. The driving forces for formation of protoimogolite rather than allophane appear to be long range Al-Al repulsive forces through oxygen.


1975 ◽  
Vol 53 (6) ◽  
pp. 939-944 ◽  
Author(s):  
Elmer C. Alyea ◽  
Abdul Malek

The synthesis and characterisation of several dibasic tridentate Schiff base ligands (H2SB) are described. Structural formulas for the isolated ligands are suggested on the basis of infrared, nuclear magnetic resonance, and mass spectral data.


2021 ◽  
Vol 15 (1) ◽  
pp. 108
Author(s):  
Zhongqi He ◽  
Mingxin Guo ◽  
Chanel Fortier ◽  
Xiaoyan Cao ◽  
Klaus Schmidt-Rohr

Conversion to biochar may be a value-added approach to recycle defatted cottonseed meal, a major byproduct from the cotton industry. In this work, complete slow pyrolysis at seven peak temperatures ranging from 300 to 600°C in batch reactors was implemented to process cottonseed meal into biochar products. Elemental analysis, attenuated total reflection Fourier transform infrared (ATR FT-IR) spectroscopy and quantitative solid state 13C nuclear magnetic resonance (NMR) spectroscopy were applied to characterize raw meal and its derived biochar products. The biochar yield and organic C and total N recoveries decreased as the peak pyrolysis temperatures was elevated. However, most of the mineral elements including P in cottonseed meal were retained during pyrolysis and became enriched in biochar as a result of the decreased mass yield. The spectral data showed that pyrolysis removed the functional groups of biopolymers in cottonseed meal, producing highly aromatic structures in biochars. With increasing pyrolysis temperature, alkyl structures decreased progressively in the biochar products and became negligible at higher temperatures (550 and 600°C). Quantitative analysis of FT IR data revealed that the values of a simple 3-band (1800,1700, and 650 cm-1)-based R reading of the biochars were linearly related to the pyrolysis temperature, and showed strong correlations with decreasing aromaticity and increasing alkyl, aliphatic C-O/N and carbonyl signal intensities in the 13C NMR spectra. Therefore, the cheaper and faster FT-IR measurement could be used as a routine conversion indicator of pyrolysis of lignocellulosic biomass instead of the more expensive and time-consuming NMR spectroscopy.


RSC Advances ◽  
2014 ◽  
Vol 4 (97) ◽  
pp. 54740-54746 ◽  
Author(s):  
A. Hariharasubramanian ◽  
Y. Dominic Ravichandran

A versatile series of lophine derivatives (1–13) were synthesized and characterized, Fourier transform infrared spectroscopy (FTIR), Liquid Chromatography-Mass Spectrometry (LC-MS), and 1H and 13C nuclear magnetic resonance (NMR) spectroscopy.


1993 ◽  
Vol 331 ◽  
Author(s):  
Mark R. Kreitz ◽  
Kathleen J. Pekarek ◽  
Edith Mathiowitz

AbstractUsing Fourier-transform infrared (FTIR) spectroscopy we have characterized a polyanhydride copolymer series composed of various ratios of the diacids 1,3-bis(p -carboxyphenoxy)propane (CPP) and sebacic acid (SA). Typical peaks corresponding to the aliphatic-aliphatic (SA-SA), aromatic-aliphatic (CPP-SA), and aromatic-aromatic (CPP-CPP) diads were found in the 1820- 1710 cm−1 wavenumber range. Further peaks corresponding to the SA-SA diads were identified in the fingerprint region at 1382, 1360, 1307, and 1286 cm−1. These peak characterizations facilitate identification of bond distribution in the CPP-SA copolymer as well as other polyanhydride copolymers, and correlate well with previously presented information obtained with nuclear magnetic resonance (NMR) spectroscopy and X-ray powder diffraction.


1982 ◽  
Vol 55 (3) ◽  
pp. 913-930 ◽  
Author(s):  
Robert C. Hirst

Abstract Fourier transform spectroscopy is without doubt one of the most important developments in spectroscopy in the last few years. Although the basic principle had been known for many years, its applications in spectroscopy became practical only because of advances in small computer technology. In the case of nuclear magnetic resonance and infrared spectroscopy, the digital computer has had a special effect, in that it has caused, or at least made possible, the total redesign of NMR and IR instrumentation based on the Fourier transform (FT) concept. Because of its advantages over conventional methods, the FT method has caused great changes in NMR and IR spectroscopy, and FT instruments have made possible the solutions to many problems which previously were technically too difficult. NMR spectroscopy was reviewed in this Journal in 1976 and infrared spectroscopy was reviewed in 1972. Developments since those reviews will be emphasized here. In a short, selective review of this type, it is necessary to omit references to many excellent contributions in the literature. For very comprehensive listings of literature references, the reader may wish to consult the biennial reviews in “Analytical Chemistry” on NMR spectroscopy, infrared spectroscopy, rubber, analysis of high polymers, and coatings.


1972 ◽  
Vol 26 (4) ◽  
pp. 430-442 ◽  
Author(s):  
Daniel A. Netzel

Recent advances in NMR spectroscopy allow one to study extremely dilute systems or nuclei which occur in low natural abundance and/or have poor sensitivity for NMR detection. This paper describes various pulse and pulse Fourier transform NMR techniques. Included in this introduction are: (1) a brief review of the nuclear relaxation phenomenon, (2) sensitivity enhancement using the pulse technique, (3) pulse instrumentation, and (4) the analytical applications of pulse Fourier transform NMR.


2019 ◽  
Vol 15 (8) ◽  
pp. 850-862
Author(s):  
Mirthala Flores-García ◽  
Juan Manuel Fernández-G. ◽  
Cristina Busqueta-Griera ◽  
Elizabeth Gómez ◽  
Simón Hernández-Ortega ◽  
...  

Background: Ischemic heart disease, cerebrovascular accident, and venous thromboembolism have the presence of a thrombotic event in common and represent the most common causes of death within the population. Objective: Since Schiff base copper(II) complexes are able to interact with polyphosphates (PolyP), a procoagulant and potentially prothrombotic platelet agent, we investigated the antiplatelet aggregating properties of two novel tridentate Schiff base ligands and their corresponding copper( II) complexes. Methods: The Schiff base ligands (L1) and (L2), as well as their corresponding copper(II) complexes (C1) and (C2), were synthesized and characterized by chemical analysis, X-ray diffraction, mass spectrometry, and UV-Visible, IR and far IR spectroscopy. In addition, EPR studies were carried out for (C1) and (C2), while (L1) and (L2) were further analyzed by 1H and 13C NMR. Tests for antiplatelet aggregation activities of all of the four compounds were conducted. Results: X-ray diffraction studies show that (L1) and (L2) exist in the enol-imine tautomeric form with a strong intramolecular hydrogen bond. NMR studies show that both ligands are found as enol-imine tautomers in CDCl3 solution. In the solid state, the geometry around the copper(II) ion in both (C1) and (C2) is square planar. EPR spectra suggest that the geometry of the complexes is similar to that observed in the solid state by X-ray crystallography. Compound (C2) exhibited the strongest antiplatelet aggregation activity. Conclusion: Schiff base copper(II) complexes, which are attracting increasing interest, could represent a new approach to treat thrombosis by blocking the activity of PolyP with a potential anticoagulant activity and, most importantly, demonstrating no adverse bleeding events.


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