Synthesis of Fluorinated Bent-Core Mesogens (BCMs) Containing the 1,2,4-Oxadiazole Ring
New fluorinated bent‐core mesogens containing the 1,2,4‐oxadiazole or 1,2,4‐triazole nucleus have been synthesized taking advantage of the ANRORC (Addition of Nucleophile, Ring‐Opening, Ring‐Closure) reactivity of 5‐perfluoroalkyl‐1,2,4‐oxadiazoles. Physical state changes of the obtained compounds w...
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Veröffentlicht in: | Journal of heterocyclic chemistry 2016-11, Vol.53 (6), p.1935-1940 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | New fluorinated bent‐core mesogens containing the 1,2,4‐oxadiazole or 1,2,4‐triazole nucleus have been synthesized taking advantage of the ANRORC (Addition of Nucleophile, Ring‐Opening, Ring‐Closure) reactivity of 5‐perfluoroalkyl‐1,2,4‐oxadiazoles. Physical state changes of the obtained compounds were characterized through DSC, POM, and SAXS. Besides the formation of a smectic mesophase, a novel behavior as organic molecular glass was evidenced for some 1,2,4‐oxadiazole derivatives. |
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ISSN: | 0022-152X 1943-5193 |
DOI: | 10.1002/jhet.2509 |