| Literature DB >> 24057655 |
Mehmet Gulcan1, Ümit Doğru2, Gülsiye Öztürk3, Abdulkadir Levent4, Esvet Akbaş5.
Abstract
A series of Schiff bases (L 1 , L 2 and L 3) were prepared by refluxing aromatic aldehydes with N-Aminopyrimidine derivatives in methanol and ethanol. The structures of synthesized compounds were characterized by FTIR, (1)H NMR, (13)C NMR and microanalysis. The electrochemical behaviors of the Schiff base ligands were also discussed. Moreover, the evaluation of absorption and emission properties of the structures were carried out in five different solvents. The products show visible absorption maxima in the range of 304-576 nm, and emission maxima from 636 to 736 nm in all solvents tested.Entities:
Keywords: N-Aminopyrimidine; Schiff base; electrochemistry; fluorescence
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Year: 2013 PMID: 24057655 DOI: 10.1007/s10895-013-1303-x
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217