scholarly journals New cholesteryl containing bent core liquid crystals

2013 ◽  
Vol 78 (5) ◽  
pp. 669-680 ◽  
Author(s):  
Cosmin-Constantin Huzum ◽  
Irina Carlescu ◽  
Gabriela Lisa ◽  
Dan Scutaru

The paper presents the synthesis and mesomorphic behavior of two new series of bent core liquid crystalline compounds based on a 1,3-dihydroxybezene core and containing a cholesteryl 6-oxyhexanoate wing. The two series were obtained by the esterification of the cholesteryl 6-(3-hydroxyphenoxy)hexanoate core with some 4-((4-(n-alkyloxy)phenyl)azo)benzoic acids (n-alkyl = n-hexyl ? n-dodecyl) or 4-(4-(n-alkyloxy)benzoyloxy)benzoic acids (n-alkyl = n-hexyl ? n-decyl). The esterification reactions were performed via the corresponding acyl chlorides or with the DCC / DMAP system. All the synthesized compounds evidenced enantiotropic liquid crystalline properties, with smectic type textures, when investigated by means of differential scanning calorimetry and polarized optical microscopy. Isotropisation and isotropic to liquid crystal transitions were relatively low (between 89 ? 1460C). The compounds containing the azo-aromatic linking group presented the largest range of stability of the mesophases (between 42 and 870C). All the investigated compounds were thermally stable in the existence range of the mesophases.

2010 ◽  
Vol 663-665 ◽  
pp. 759-762 ◽  
Author(s):  
Qing Lan Ma ◽  
Yuan Ming Huang

A series of cholesterol liquid crystal compounds was synthesized. Phase-transition temperatures and mesomorphic textures of these synthesized compounds were characterized with differential scanning calorimetry and polarized optical microscopy, respectively. In these molecules the terminal ester chains CnH2n-1COO-, where n was the number of carbon atoms in the terminal ester chains, were linked to the cholesterol core. All of the synthesized cholesterol compounds exhibited mesophases for the first heating. However, as temperature decreased from their clearing points, their micrographs can also be divided into two categories, the first category exhibits branch-like mesophase textures for n in the range of 1-10 while the second category exhibits branch-like crystal textures for n in the range of 11-18.


2010 ◽  
Vol 663-665 ◽  
pp. 787-790 ◽  
Author(s):  
Qing Lan Ma ◽  
Yuan Ming Huang

A bent-core liquid crystal compound N,N-bis (4-propoxybenzylidene)benzene- 1,3-diamine was synthesized. Phase transition properties of the synthesized compound with the deferent heating rate were characterized with differential scanning calorimetry and polarized optical microscopy. , respectively. Our results demonstrated that the bent-core compound exhibited the completely undivided multi-phases in heating-rate ranges from 1oC/min to 6oC/min while it showed a broad-peak crystal phase in higher heating-rate ranges of 7-10oC/min for the first heating.


2010 ◽  
Vol 428-429 ◽  
pp. 247-250 ◽  
Author(s):  
Yuan Ming Huang ◽  
Qing Lan Ma ◽  
Bao Gai Zhai

The influence of cooling rate on the phase transitions of a three-benzene-ring containing bent-core liquid crystal 1,3-phenylene-bis[4-(hexylcarboyloxyl)benzylideneamine] has been investigated by means of differential scanning calorimetry and polarized optical microscopy. Our results show that the cooling rates in the second cooling run pose significant effects on the phase transitions of the bent-core liquid crystal despite the cooling rates in the first cooling run pose little effects on the phase transitions. In the second cooling run, the banana phases survived only when the cooling rates were in the range of 14~15oC/min whereas both slow cooling rates which were less than 13oC/min and fast cooling rates which were higher than 16oC/min made the banana phases disappeared.


2011 ◽  
Vol 181-182 ◽  
pp. 96-101 ◽  
Author(s):  
Qing Lan Ma ◽  
Bao Gai Zhai ◽  
Rui Xiong ◽  
Yuan Ming Huang

Rod-like liquid crystals N-(4-methoxybenzylidene)-4-n-alkoxybenzenamine (MBnBA,n= 1, 2, 10) were synthesized and then were investigated by differential scanning calorimetry, polarizing optical microscopy, ultraviolet-visible spectrophotometry and fluorescence spectroscopy. Our results demonstrated that the dilute tetrahydrofuran solutions of each member in the family of MBnBA could give off blue fluorescence under the 325 nm excitation. The calculated electronic structures revealed that the fluorescence recorded at 469 nm (2.65 eV) was the result ofπ* →ntransitions in the molecules of the synthesized liquid crystals MBnBA.


2017 ◽  
Vol 25 (9) ◽  
pp. 669-676 ◽  
Author(s):  
Danesh Roudini

Side-chain liquid crystalline polythiophenes were synthesised and the effects of the mesogenic units on the structure and electronic properties of the polymers were studied. The liquid crystal properties of the polymer films were studied using polarised hot-stage optical microscopy and differential scanning calorimetry, and X-ray diffractometry was used to investigate the effect of a magnetic field on the monomers and polymers.


2010 ◽  
Vol 428-429 ◽  
pp. 167-170
Author(s):  
Yuan Ming Huang

A three-ring containing bent-core compound 1,3-phenylene-bis(4-butoxybenzylidene amine) was synthesized and characterized with differential scanning calorimetry and polarized optical microscopy. It exhibited mesophases in the temperature range of 48-54oC for the first cyclic heating and cooling. Our results demonstrated that three-ring containing bent-core molecules can form mesophases.


1990 ◽  
Vol 45 (7) ◽  
pp. 1084-1090 ◽  
Author(s):  
Klaus Praefcke ◽  
Bernd Kohne ◽  
Andreas Eckert ◽  
Joachim Hempel

Six S,S-dialkyl acetals 2a-f of inosose (1), tripodal in structure, have been synthesized, characterized and investigated by optical microscopy and differential scanning calorimetry (d.s.c.). The four S,S-acetals 2c-f with sufficiently long alkyl chains are thermotropic liquid crystalline; 2 e and 2 f are even dithermomesomorphic. Each of these four inosose derivatives 2c-f exhibits monotropically a most likely cubic mesophase (MI); in addition 2e and 2f show enantiotropically a hexagonal mesophase (Hx) with a non-covalent, supramolecular H-bridge architecture. Whereas the nature of the optically isotropic mesophase MI needs further clarification the stable high temperature mesophase Hx of 2 e and 2 f has been established by a miscibility test using a sugar S,S-dialkyl acetal also tripodal in structure and with a Hx phase proved by X-ray diffraction, but in contrast to 2 with an acyclic hydrophilic part. Similarities of structural features between the Hx-phases of 2e and 2f as well as of other thermotropic and lyotropic liquid crystal systems are discussed briefly.


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