Electrochemical studies and semiempirical calculations on π-conjugated dienones and heterocyclic nitrogen containing donor ligand molecules was written by Vatsadze, S.;Al-Anber, M.;Thiel, W. R.;Lang, H.;Holze, R.. And the article was included in Journal of Solid State Electrochemistry in 2005.Safety of 2,5-Di(pyridin-4-yl)-1,3,4-oxadiazole This article mentions the following:
Reduction potentials for the first electron transfer to a broad selection of nitrogen containing bi- and polydentate mols. considered as potential ligands have been determined Results are compared with data obtained with semiempirical and UV-Vis spectroscopic data. Close correlations for the investigated mols. are observed Systematic differences in properties of mols. with and without the keto moiety can be explained by invoking MO and surface interaction arguments. Similar structural arguments can be used to explain the behavior of 2,4,6-tripyridin-2-yl[1,3,5]triazine. UV-Vis data match closely those derived from HOMO-LUMO calculations for these mols. In the experiment, the researchers used many compounds, for example, 2,5-Di(pyridin-4-yl)-1,3,4-oxadiazole (cas: 15420-02-7Safety of 2,5-Di(pyridin-4-yl)-1,3,4-oxadiazole).
2,5-Di(pyridin-4-yl)-1,3,4-oxadiazole (cas: 15420-02-7) belongs to pyridine derivatives. Pyridines are an important class of heterocycles and occur in polysubstituted forms in many naturally occurring biologically active compounds, drug molecules and chiral ligands. Pyridine groups exist in countless molecules, and their applications include catalysis, drug design, molecular recognition, and natural product synthesis.Safety of 2,5-Di(pyridin-4-yl)-1,3,4-oxadiazole