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Synthesis of new allylidene amino phenol-containing Schiff bases and metal complex formation using trimethinium salts
An efficient route for the synthesis of novel Schiff bases from the condensation reaction of 2-substituted 1,3-bis(dimethylamino)-trimethinium salts with diverse aminophenols in the presence of triethylamine in EtOH at reflux is described. Complexes of transition metals with Schiff base ligand (L) 3...
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Published in: | RSC advances 2021-06, Vol.11 (35), p.21695-2171 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | An efficient route for the synthesis of novel Schiff bases from the condensation reaction of 2-substituted 1,3-bis(dimethylamino)-trimethinium salts with diverse aminophenols in the presence of triethylamine in EtOH at reflux is described. Complexes of transition metals with Schiff base ligand (L)
3c
, having the donor atom set N
2
O
2
, were studied. The ultraviolet spectral behavior of the complexes in DMSO was investigated and the
λ
max
of these compounds was examined. The structure of the new compounds was confirmed based on their spectral data from IR,
1
H NMR and
13
C NMR, mass spectra, and elemental analysis.
An efficient route for the synthesis of novel Schiff bases from the condensation reaction of 2-substituted 1,3-bis(dimethylamino)-trimethinium salts with diverse aminophenols in the presence of triethylamine in EtOH at reflux is described. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/d1ra04214a |