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  Effects of benzoyl group substituents on the mesomorphic properties of 5-alkoxy-2-benzoylaminotropones
 
 
Titel: Effects of benzoyl group substituents on the mesomorphic properties of 5-alkoxy-2-benzoylaminotropones
Auteur: Mori, Akira
Uno, Katsuyuki
Kubo, Kanji
Kato, Nobuo
Takeshita, Hitoshi
Hirayama, Ken
Ujiie, Seiji
Verschenen in: Liquid crystals
Paginering: Jaargang 31 (2004) nr. 2 pagina's 285-294
Jaar: 2004-02
Inhoud: Three types of 5-alkoxy-2-benzoylaminotropones, containing an electron-donating group and seven types of derivatives with electron-withdrawing groups on the benzoyl group, were prepared in order to study the thermal ranges of the mesophases exhibited. The troponoid amides had higher transition temperatures than the corresponding troponoid esters and benzenoid amides. From the 1H NMR spectroscopic measurements and X-ray crystallographic analysis of 5-butoxy-2-(4-methoxybenzoylamino)tropone, it was observed that the benzoyl carbonyl group faced to the H-3 of the tropone ring to form an intramolecular hydrogen bond between the tropone carbonyl and the amide NH groups. The intramolecular hydrogen bonding of the troponoid amides made the molecules flat, inducing strong π-π intermolecular interactions between head-to-tail dimers and so reduced the possibility of intermolecular hydrogen bonding between the NH group and the carbonyl group of neighbouring molecules so decreasing melting points. Electron-donating groups enhanced the appearance of nematic phases while electron-withdrawing groups promoted smectic A phases.
Uitgever: Taylor & Francis
Bronbestand: Elektronische Wetenschappelijke Tijdschriften
 
 

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