Synthesis and spectral characterization of macrocyclic lanthanide(III) Complexes of an 18-Membered Tetraaza Tetraimine Schiff Bases

2019 ◽  
Vol 18 (1) ◽  
pp. 1-13
Author(s):  
B. Anna Benedict
2013 ◽  
Vol 12 (1) ◽  
pp. 87-104 ◽  
Author(s):  
Narayanachar ◽  
Shreedhar D. Dhumwad ◽  
Srinivas Mutalik ◽  
Mallinath H. Hugar ◽  
Praveen N. Naik

Author(s):  
Balram Prasad Baranwal ◽  
Kiran Tripathi ◽  
Alok Kumar Singh ◽  
Saurabh Tripathi

2021 ◽  
Vol 37 (3) ◽  
pp. 759-762
Author(s):  
Shaila Wagh ◽  
B.R. Patil

New Schiff bases derived by the condensation of methyl, chloro, and bromo substituted 2' hydroxy propiophenones with aliphatic and aromatic amines have been synthesized. The Schiff bases are yellow solids with sharp melting points. Schiff bases The spectral characterization of these newly synthesized Schiff base ligands has been done.These Schiff bases were characterized by IR spectroscopy, Nuclear magnetic resonance spectroscopy, UV spectroscopy, and Mass spectroscopy. IR spectra confirmed the presence of the phenolic OH group and azomethine group.


2007 ◽  
Vol 62 (5) ◽  
pp. 717-720 ◽  
Author(s):  
Hassan Hosseini Monfared ◽  
Omid Pouralimardan ◽  
Christoph Janiak

Abstract Reactions of 2,4-dinitrophenylhydrazine with salicylaldehyde, pyridine-2-carbaldehyde and 2- aminobenzophenone in methanol result in the hydrazone Schiff base ligands salicylaldehyde-, pyridine- 2-carbaldehyde-, and 2-aminobenzophenone-2,4-dinitrophenylhydrazone, respectively. Crystals of salicylaldehyde-2,4-dinitrophenylhydrazone are monoclinic, space group P21/c, a = 13.820(3), b = 4.3515(9), c = 25.159(7) Å , β = 123.01(2)° with Z = 4. The molecular packing is mostly a zigzag or herring-bone pattern.


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