You have requested a machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Neither SPIE nor the owners and publishers of the content make, and they explicitly disclaim, any express or implied representations or warranties of any kind, including, without limitation, representations and warranties as to the functionality of the translation feature or the accuracy or completeness of the translations.
Translations are not retained in our system. Your use of this feature and the translations is subject to all use restrictions contained in the Terms and Conditions of Use of the SPIE website.
1 January 1998X-ray investigation of new isomeric oxadiazoles
An x-ray investigation has been performed on five new 2,5- disubstituted 1,2,4-oxadiazoles with reversed structures containing 4-amylbiphenyl-, trans-4-amylcyclohexylphenyl- and 2-halophenyl- as substituents. The aim was to confirm the data about the phase sequence, obtained via polarizing microscopy and differential scanning calorimetry, and to measure the structural parameters. Through x-ray diffraction technique, all substances showed only the nematic mesophase. Moreover, it was proved that some enthalphy variations previously attributed to crystal-crystal transitions are in fact due either to the rearrangement of the lattice or to the coalescence of the grains. However, for some substances, a second crystalline from c' appeared at the melting point, on cooling from the isotropic phase. C' turned out to be different from the starting form C1 of the sample, which had no thermal cycle before.
The alert did not successfully save. Please try again later.
Oriano Francescangeli, L. A. Karamysheva, Sofia I. Torgova, A. Sparavigna, Alfredo Strigazzi, "X-ray investigation of new isomeric oxadiazoles," Proc. SPIE 3319, Liquid Crystals: Chemistry and Structure, (1 January 1998); https://doi.org/10.1117/12.301271