Hydrogen-bonded oxadiazole mesogens was written by Martin, Pamela J.;Bruce, Duncan W.. And the article was included in Liquid Crystals in 2007.Recommanded Product: 15420-02-7 This article mentions the following:
Hydrogen-bonded analogs of recently reported biaxial nematic oxadiazoles have been prepared These are obtained by having oxadiazole derivatized with either one or two pyridines, leading either to sym. or unsym. materials complexed using several different benzoic acids. The new materials were studied by optical microscopy and DSC and were found to show N and SmA phases, i.e. mesomorphism characteristic of a calamitic rather than a bent-core mesogen. This mesomorphism is discussed in terms of the flexibility of the complexes and the bend angle at the center of the complexes. In the experiment, the researchers used many compounds, for example, 2,5-Di(pyridin-4-yl)-1,3,4-oxadiazole (cas: 15420-02-7Recommanded Product: 15420-02-7).
2,5-Di(pyridin-4-yl)-1,3,4-oxadiazole (cas: 15420-02-7) belongs to pyridine derivatives. Pyridine’s the lone pair does not contribute to the aromatic system but importantly influences the chemical properties of pyridine, as it easily supports bond formation via an electrophilic attack. Many analogues of pyridine are known where N is replaced by other heteroatoms . Substitution of one C–H in pyridine with a second N gives rise to the diazine heterocycles (C4H4N2), with the names pyridazine, pyrimidine, and pyrazine.Recommanded Product: 15420-02-7