Influence of substituting thioester for ester group and alkyloxy for alkyl chain on liquid-crystalline polymorphism of certain azobenzene derivatives

2009 ◽  
Vol 36 (2) ◽  
pp. 187-195 ◽  
Author(s):  
Urszula Jarek-Mikulska ◽  
Zbigniew Galewski
Keyword(s):  
Liquid Crystalline ◽  
Alkyl Chain ◽  
Ester Group ◽  
Crystalline Polymorphism ◽  
Azobenzene Derivatives

Influence of terminal groups on liquid-crystalline polymorphism of selected azobenzene derivatives

2013 ◽  
Vol 41 (1) ◽  
pp. 113-125 ◽  
Author(s):  
Marta Podruczna ◽  
Anna Hofmańska ◽  
Izabela Niezgoda ◽  
Damian Pociecha ◽  
Zbigniew Galewski
Keyword(s):  
Liquid Crystalline ◽  
Crystalline Polymorphism ◽  
Azobenzene Derivatives

scholarly journals New azobenzene liquid crystal with dihydropyrazole heterocycle and photoisomerization studies

2020 ◽  
Vol 7 (7) ◽  
pp. 200474
Author(s):  
Xiaoxuan Wang ◽  
Zhaoxia Li ◽  
Haiying Zhao ◽  
Shufeng Chen
Keyword(s):  
Liquid Crystal ◽  
Liquid Crystalline ◽  
Ester Group ◽  
Azo Compounds ◽  
Scanning Calorimetry ◽  
Polarizing Microscopy ◽  
Mesogenic Unit ◽  
Crystal Properties ◽  
Azobenzene Derivatives ◽  
Long Chain

New azobenzene derivatives with dihydropyrazole heterocycle have been prepared and characterized. According to thermal polarizing microscopy and differential scanning calorimetry studies, the compounds consisting of four linearly linked rings and a long alkoxy chain on the azobenzene side ( 3a-8 and 3a-14 ) displayed no liquid crystal properties. When the length of mesogenic unit increased to five rings, except for compound 5a-8 , all compounds from 5a-10 to 5a-16 containing a long chain of 10–16 carbon atoms on the side of ester group displayed liquid crystalline properties, and the mesogenic domain gradually narrowed with increase of the chain length. However, in the case of the molecule with long alkoxy chains on both sides, only 5c-16 with a long chain of 16 carbon atoms exhibited liquid crystal behaviour. In addition, these azo compounds underwent isomerization from E to Z under ultraviolet irradiation and then thermal back relaxation slowly in the dark, which can be recycled many times.

Charge mobility in discotic liquid crystalline porphyrins and phthalocyanines measured by PR-TRMC

2003 ◽  
Vol 07 (05) ◽  
pp. 342-350 ◽  
Author(s):  
John M. Warman ◽  
Jessica E. Kroeze ◽  
Pieter G. Schouten ◽  
Anick M. van de Craats
Keyword(s):  
Conjugated Polymers ◽  
Carrier Mobility ◽  
Liquid Crystalline ◽  
Alkyl Chain ◽  
Charge Carrier Mobility ◽  
Chain Structure ◽  
Coupling Element ◽  
Time Resolved ◽  
Liquid Crystalline Phases ◽  
Conductive Properties

The pulse-radiolysis time-resolved microwave conductivity technique, “PR-TRMC”, has been used to determine the charge carrier mobility within columnar stacks of mesomorphic discotic porphyrins and phthalocyanines. The influences of temperature, morphology and variations in the primary molecular structure are demonstrated and discussed. Both the mesomorphic and conductive properties are shown to be dramatically influenced by subtle changes in the peripheral alkyl chain structure or the core-to-chain coupling element. Mobilities close to 1 cm2.V−1.s−1 are found in crystalline solids, and well in excess of 0.1 cm2.V−1.s−1 in columnar, liquid crystalline phases. These values which are even larger than those determined by PR-TRMC for conjugated polymers and similar to values found for electrons and holes in organic single crystals.

scholarly journals Phase Transitions of Side Chain Liquid Crystalline Polymers Having a Terminal Alkyl Chain.

1993 ◽  
Vol 50 (9) ◽  
pp. 687-691 ◽  
Author(s):  
Seiji UJIIE ◽  
Tamami FUKUI ◽  
Kazuko HIGAKI ◽  
Satoshi TAKAHASHI ◽  
Kazuyoshi IIMURA
Keyword(s):  
Phase Transitions ◽  
Liquid Crystalline ◽  
Alkyl Chain ◽  
Liquid Crystalline Polymers ◽  
Side Chain ◽  
Crystalline Polymers

scholarly journals Influence of alkyl chain length and fluorine atoms substitution on infrared spectra of chiral liquid crystalline esters

2017 ◽  
Vol 66 (3) ◽  
pp. 63-74
Author(s):  
Anna Drzewicz ◽  
Marzena Tykarska ◽  
Magdalena Żurowska
Keyword(s):  
Molecular Structure ◽  
Infrared Spectroscopy ◽  
Liquid Crystals ◽  
Infrared Spectra ◽  
Crystalline Phase ◽  
Liquid Crystalline ◽  
Alkyl Chain ◽  
Alkyl Chain Length ◽  
Rigid Core ◽  
Helicoidal Structure

The infrared spectra were registered for series of three-ring liquid crystalline esters, differing in the structure of alkyl chain, in the substitution of benzene ring by fluorine atoms and in the type of helicoidal structure in the chiral smectic CA phase with antiferroelectric properties. The influence of molecular structure on the shift of signals coming from carbonyl group, located in the rigid core, was observed. Keywords: liquid crystals, helicoidal structure, chiral smectic CA phase, antiferroelectric crystalline phase, infrared spectroscopy

scholarly journals Influence of molecular structure on helicoidal structure and NMR spectra of chiral liquid crystalline esters

2017 ◽  
Vol 66 (2) ◽  
pp. 25-35
Author(s):  
Anna Drzewicz ◽  
Marzena Tykarska ◽  
Mateusz Szala ◽  
Magdalena Żurowska
Keyword(s):  
Molecular Structure ◽  
Nmr Spectra ◽  
Liquid Crystalline ◽  
Room Temperature ◽  
Alkyl Chain ◽  
Light Reflection ◽  
13C Nmr Spectra ◽  
1H And 13C Nmr ◽  
Antiferroelectric Phase ◽  
Helicoidal Structure

Three-ring chiral liquid crystalline compounds, forming antiferroelectric phase, differing in the structure of alkyl chain and in the substitution of benzene ring by fluorine atoms were studied. The measurements of helical pitch, based on the selective light reflection phenomenon, were performed as well as 1H and 13C NMR spectra at room temperature were registered. The influence of molecular structure as well as the type of helicoidal structure on the chemical shift of signals coming from chiral center was observed. Keywords: liquid crystals, helicoidal structure, nuclear magnetic resonance, antiferroelectric phase

Research on Some Novel Functional Azobenzene Derivatives with Alkyl Chains and Different Substituted Groups

2011 ◽  
Vol 474-476 ◽  
pp. 537-542
Author(s):  
Ti Feng Jiao ◽  
Xu Hui Li ◽  
Jing Xin Zhou ◽  
Yuan Yuan Xing ◽  
Jing Ren
Keyword(s):  
Alkyl Chain ◽  
Uv Light ◽  
Molecular Structures ◽  
Functional Material ◽  
Alkyl Chains ◽  
Temperature Ranges ◽  
The Difference ◽  
Structural Influence ◽  
Azobenzene Derivatives ◽  
Base Group

Two functional azobenzene derivatives with alkyl chains and different substituted groups have been synthesized and their photoisomerization have also been investigated. It has been found that depending on the alkyl chain and different substituted groups, the formed azobenzene derivatives showed different properties, indicating distinct regulation of molecular skeletons. UV and IR data confirmed commonly the characteristic absorption of alkyl chain and aromatic segments in molecular structures. Thermal analysis demonstrated that the structural influence of both compounds in different temperature ranges. The difference of thermal stability is mainly attributed to the formation of Schiff base group and different substituent groups in molecular structure. The photoisomerization of these compounds both in solution and in cast film can undergo trans-to-cis isomerization by UV light irradiation, depending on different substituted groups. The present results have demonstrated that the special properties of azobenzene derivatives can be effectively turned by modifying molecular structures of objective compounds with proper substituted groups, which show potential application in functional material field.

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