Lateral substitution as effective tool for tuning self-organising behaviour of chiral mesogens

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F21%3A00551199" target="_blank" >RIV/68378271:_____/21:00551199 - isvavai.cz</a>
Result on the web
<a href="http://hdl.handle.net/11104/0327453" target="_blank" >http://hdl.handle.net/11104/0327453</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.18083/LCAppl.2021.4.23" target="_blank" >10.18083/LCAppl.2021.4.23</a>

Result language
angličtina
Original language name
Lateral substitution as effective tool for tuning self-organising behaviour of chiral mesogens
Original language description
In this mini-review we discuss a relatively broad sub-class of chiral calamitic liquid crystalline materials derived from the lactic acid and will give some specific examples on effective tuning of their mesomorphic and electro-optical behaviour by using various types of lateral substitution on the molecular core. The fluorine, chlorine, bromine and iodine atoms, as well as the methyl and methoxy groups are used as lateral substituents on the phenyl ring far from the chiral lactate group. The materials discussed in this work can be potentially used as smart dopants for the design of advanced multicomponent mixtures targeted for future applications in opto-electronics and photonics.
Czech name
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Czech description
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Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10302 - Condensed matter physics (including formerly solid state physics, supercond.)

Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2021
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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