Spectroscopic Study and Semi-empirical Calculations of Tautomeric Forms of Schiff Bases Derived from 2-hydroxy- 1-naphthaldehyde and Substituted 2-aminothiophene

2010 ◽  
Vol 3 ◽  
pp. 1-8 ◽  
2010 ◽  
Vol 7 (3) ◽  
pp. 1045-1054 ◽  
Author(s):  
Sonal Agnihotri ◽  
Kishor Arora

Schiff bases were obtained usingp-trimethoxy benzaldehyde,p-hydroxyl benzaldehyde and 2-amino pyridine to prepare new complexes of thorium(IV) and dioxouranium(VI) metals by various anions. The synthesized ligands and complexes were analytically studied through spectral studies, elemental analysis conductance measurements along with semi empirical and thermogravimetric methods. The complexes were assigned various coordination numbers ranging from 6-10 on the basis of these studies.


1991 ◽  
Vol 279 (3) ◽  
pp. 759-767 ◽  
Author(s):  
M A Vázquez ◽  
F Muñoz ◽  
J Donoso ◽  
F García Blanco

We recorded the absorption spectra of the Schiff bases of pyridoxal 5′-phosphate (PLP) and 5′-deoxypyridoxal (DPL) with dodecylamine (DOD) at different pH values. By applying deconvolution techniques to the spectra and analysing their different components we found that the above-mentioned Schiff bases in aqueous solutions of pH 7 adopted a conformation in which the pyridine ring is embedded in a very hydrophobic medium from which water is virtually completely excluded. This conformation in the same as that adopted by PLP when it acts as coenzyme for some enzymes such as glycogen phosphorylase. The experimental results obtained also show such a conformation to be highly favoured but sensitive to the protonation of the pyridine nitrogen, which makes the aromatic ring more readily accessible to the solvent.


Author(s):  
Hasan Nazir ◽  
Cengiz Arici ◽  
Kaan C. Emregül ◽  
Orhan Atakol

AbstractThe molecular structures of N-(2-hydroxy ethyl)-3,5-dinitrosalicylaldimine and N-N′-bis(acetophe-nylketimine)-1,4-diaminobuthane were determined using X-ray diffraction. It was established using the difference Fourier map that the phenolic hydrogens were situated on the iminic nitrogen. Identical observations of the molecular structure were made for similar Schiff bases in literature, and it was established that this situation was not in agreement with the IR and NMR results. The molecular structure of N-(4-hydroxylphenyl)-benzaldimine was determined using X-ray diffraction for comparison. Similar compounds were prepared and their FTIR spectra were investigated.


2021 ◽  
Vol 1818 (1) ◽  
pp. 012014
Author(s):  
Orass Abdulhadi Hussein ◽  
Dawood M. Khudhair ◽  
Alyaa A. Alrazaq A. Aljbar

Polymer ◽  
2004 ◽  
Vol 45 (26) ◽  
pp. 8871-8879 ◽  
Author(s):  
Dongdong Feng ◽  
Shanfeng Wang ◽  
Qixin Zhuang ◽  
Pingping Wu ◽  
Zhewen Han

2012 ◽  
Vol 28 (4) ◽  
pp. 1871-1876
Author(s):  
B.K. RAI ◽  
ARUN KUMAR ◽  
AKHILESH BALUNI

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