Issue 42, 2015

3-Substituted 6-oxoverdazyl bent-core nematic radicals: synthesis and characterization

Abstract

A series of bent-core derivatives of 6-oxoverdazyl 1[12] was synthesized and mesogenic properties were investigated in the pure form and in binary mixtures. Results demonstrate that the effectiveness of the C(3) substituent in nematic phase stabilization follows the order: COOMe > m-FC6H4 > Ph > thienyl > o-FC6H4, which is consistent with steric parameters established with DFT computational methods and opposite to the order of the appearance of a re-entrant isotropic phase. The effect of alkyl chain elongation on mesogenic properties and the effect of C(3) substituent on electronic absorption spectra are also investigated.

Graphical abstract: 3-Substituted 6-oxoverdazyl bent-core nematic radicals: synthesis and characterization

Supplementary files

Article information

Article type
Paper
Submitted
08 Mar 2015
Accepted
30 Mar 2015
First published
30 Mar 2015

RSC Adv., 2015,5, 33328-33333

Author version available

3-Substituted 6-oxoverdazyl bent-core nematic radicals: synthesis and characterization

S. Ciastek, M. Jasiński and P. Kaszyński, RSC Adv., 2015, 5, 33328 DOI: 10.1039/C5RA04119H

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