Diphenylthiophenes as central part for the design of bent-core liquid crystalline compounds.

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F18%3A43916610" target="_blank" >RIV/60461373:22310/18:43916610 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/68378271:_____/18:00495482

Výsledek na webu

<a href="http://dx.doi.org/10.1016/j.molliq.2018.02.009" target="_blank" >http://dx.doi.org/10.1016/j.molliq.2018.02.009</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.molliq.2018.02.009" target="_blank" >10.1016/j.molliq.2018.02.009</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Diphenylthiophenes as central part for the design of bent-core liquid crystalline compounds.

Popis výsledku v původním jazyce

New type of bent-core molecules based on the 2,5-diphenylthiophene and 3,4-diphenylthiophene central cores have been synthesized as potential liquid crystalline compounds. We have varied non-linear 2,5-diphenylthiophene molecular core as a potential source of central unit of bent-core mesogens and for the first time introduced 3,4-diphenylthiophene central core in the design of V-shaped liquid crystals. Unfortunately, no mesogenicity has been observed for the 3,4-diphenylthiophene-based compounds. The effect of the lateral substitution on the central thiophene in 2,5-diphenylthiophene derivatives has been investigated. We have succeeded in substantial decrease of transition temperatures and the nematic phase has been observed for several compounds.

Název v anglickém jazyce

Diphenylthiophenes as central part for the design of bent-core liquid crystalline compounds.

Popis výsledku anglicky

New type of bent-core molecules based on the 2,5-diphenylthiophene and 3,4-diphenylthiophene central cores have been synthesized as potential liquid crystalline compounds. We have varied non-linear 2,5-diphenylthiophene molecular core as a potential source of central unit of bent-core mesogens and for the first time introduced 3,4-diphenylthiophene central core in the design of V-shaped liquid crystals. Unfortunately, no mesogenicity has been observed for the 3,4-diphenylthiophene-based compounds. The effect of the lateral substitution on the central thiophene in 2,5-diphenylthiophene derivatives has been investigated. We have succeeded in substantial decrease of transition temperatures and the nematic phase has been observed for several compounds.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10302 - Condensed matter physics (including formerly solid state physics, supercond.)

Projekt

<a href="/cs/project/GA16-12150S" target="_blank" >GA16-12150S: Samouspořádávající se vícefunkční fotosenzitivní materiály</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2018

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Journal of Molecular Liquids

ISSN

0167-7322

e-ISSN

—

Svazek periodika

267

Číslo periodika v rámci svazku

SI

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

8

Strana od-do

496-503

Kód UT WoS článku

000447575800068

EID výsledku v databázi Scopus

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