1978
DOI: 10.1002/bbpc.19780820810
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Experimentelle Prüfung von approximativen Chiralitätsfunktionen [1, 2] am Beispiel der induziert cholesterischen Lösung chiraler Methan‐Derivate

Abstract: Die R-Cotton-Effekte von cholesterischen LBsungen, die durch chirale Methan-Derivate in nematischen Phasen induziert werden. stellen Chiralitltsbeobachtungen dar, die durch approximative Chiralitatsfunktionen in guter Naherung beschrieben werden konnen. Die untersuchten System sind Schiffsche Basen, gelost in EBBA/MBBA sowie in Licristal? Nur fur die Losung der Schiffschen Basen in EBBA/MBBA lassen sich bei Anwendung von Chiralitatsfunktionen ligandenspezifische Zahlen ermitteln.Certain chiral methane-derivati… Show more

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Cited by 10 publications
(2 citation statements)
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“…This is usually achieved by addition of chiral dopants to either shorten or lengthen the pitch length (the latter is sometimes termed compensation). Questions might also be raised about how a given chiral dopant allows transfer of chirality to the phase; for optimal transfer of the twist, it is best to use a dopant that has some structural similarity with the host mixture [28][29][30][31]. • How does the pitch change with temperature?…”
Section: Formulation and Application Of Chiral Nematic Liquid Crystalmentioning
confidence: 99%
See 1 more Smart Citation
“…This is usually achieved by addition of chiral dopants to either shorten or lengthen the pitch length (the latter is sometimes termed compensation). Questions might also be raised about how a given chiral dopant allows transfer of chirality to the phase; for optimal transfer of the twist, it is best to use a dopant that has some structural similarity with the host mixture [28][29][30][31]. • How does the pitch change with temperature?…”
Section: Formulation and Application Of Chiral Nematic Liquid Crystalmentioning
confidence: 99%
“…The first step involves the FeCl 3 catalyzed coupling of (S)-(+)-2-methylbutyl bromide (10) and 4-biphenylmagnesiumbromide (formed by transmetalation from previously generated (S)-(+)-2-methylbutylmagnesiumbromide), to give the chiral biphenyl (29); this was then brominated to give (S)-(+)-4-(2-methylbutyl)-4 -bromobiphenyl (30), which was eventually cyanated using copper cyanide to give the chiral biphenyl 25. An improved synthesis of 25 was described later, applying a Kumada type coupling of 4-bromobiphenyl and (R)-2-methylbutylmagnesiumbromide to give 29 [122,123].…”
Section: Stable Phenyl Biphenyl Terphenyl and Phenylethylbiphenyl mentioning
confidence: 99%