Synthesis and Characterization of Some Dibasic Tridentate Schiff Base Ligands

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.

Author(s):  
Garima Shrivastava ◽  
Manjul Shrivastava

New Schiff base (2-[(1H-benzimidazol-2-ylimino) methyl]-4,6- diiodophenol) was synthesized by the condensation of aryl/hetero aromatic aldehyde (3,5diiodosalicylaldehyde) with 2- amino benzimidazole under conventional and microwave conditions and characterized through IR, HNMR and Mass spectral data and CHN analysis


1987 ◽  
Vol 65 (9) ◽  
pp. 2069-2076 ◽  
Author(s):  
Gerald Oliver Aspinall ◽  
Lev Khondo ◽  
Bruce Alan Williams

Reduction of uronic acid residues in permethylated polysaccharides from Sterculiaurens and S. caudata gums, followed by transformation of the resulting hexose into 6-deoxy-6-iodohexose residues, affords modified polysaccharides that undergo depolymerization on treatment with zinc dust. The main products after reduction with sodium borohydride are hexenitolterminated oligosaccharides. Their structures have been assigned as members of a series of O-[α-L-rhamnopyranosyl]-(1 → 3)-1,2-dideoxyhex-1-enitol derivatives, with and without attendant β-D-galactopyranosyl substituents, on the basis of nuclear magnetic resonance and mass spectral data and compositional analysis of trideuteriomethylated derivatives. The structures of the polysaccharides have been reassessed in the light of these and other experiments, and may now be formulated as containing a backbone of alternating 4-linked α-D-galacturonic acid and 2-linked α-L-rhamnopyranose residues bearing a minimum of three types of side chains attached at specific sites. Characterization of some of the degradation products provides evidence that limited degradation had occurred during methylation of the glycuronans.


1998 ◽  
Vol 63 (3) ◽  
pp. 371-377 ◽  
Author(s):  
Emilia Luks ◽  
Wanda Radecka-Paryzek

The partial Schiff base condensation reactions between 2,6-diacetylpyridine and 1,3-phenylenediamine in the presence of scandium(III), yttrium(III) and lanthanum(III) ions as template agents afford new mono- and dinuclear hexadentate complexes of podate type, depending on the molar ratio of starting materials used in the synthesis. They were characterized by IR, UV-VIS, 1H NMR, and mass spectral data as well as by thermogravimetric and elemental analyses.


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