| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5228371 | Tetrahedron | 2008 | 6 Pages | 
Abstract
												Three new α,αâ²-diimine ligands were synthesized based on condensation of 1,10-phenanthroline-5,6-dione with 1,2-phenylenediamine derivatives using different approaches. All compounds were fully characterized by IR, 1H and 13C NMR, UV-visible, and MS spectroscopies. We report the first example of a dipyrido[3,2-f:2â²,3â²-h]quinoxalino[2,3-b]quinoxaline, which exhibits a strong absorption at 430 nm and an interesting electrochemical behavior. These new molecules may have biological potential and are of synthetic and technological importance.
Graphical abstractDownload full-size image
Related Topics
												
													Physical Sciences and Engineering
													Chemistry
													Organic Chemistry
												
											Authors
												Fabio da Silva Miranda, Aline Maria Signori, Juliano Vicente, Bernardo de Souza, Jacks Patrick Priebe, Bruno Szpoganicz, Norberto Sanches Gonçalves, Ademir Neves, 
											![First Page Preview: Synthesis of substituted dipyrido[3,2-a:2â²,3â²-c]phenazines and a new heterocyclic dipyrido[3,2-f:2â²,3â²-h]quinoxalino[2,3-b]quinoxaline Synthesis of substituted dipyrido[3,2-a:2â²,3â²-c]phenazines and a new heterocyclic dipyrido[3,2-f:2â²,3â²-h]quinoxalino[2,3-b]quinoxaline](/preview/png/5228371.png)