Blue Fluorescent Liquid Crystal N-(4-methoxybenzylidene)-4-n-alkoxybenzenamine

2011 ◽  
Vol 181-182 ◽  
pp. 96-101 ◽  
Author(s):  
Qing Lan Ma ◽  
Bao Gai Zhai ◽  
Rui Xiong ◽  
Yuan Ming Huang
Keyword(s):  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
Liquid Crystals ◽  
Fluorescence Spectroscopy ◽  
Optical Microscopy ◽  
Electronic Structures ◽  
Blue Fluorescence ◽  
Scanning Calorimetry ◽  
Visible Spectrophotometry ◽  
The Family

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.

Synthesis and Mesomorphic Properties of a Series of Cholesteric Liquid Crystals

2010 ◽  
Vol 663-665 ◽  
pp. 759-762 ◽  
Author(s):  
Qing Lan Ma ◽  
Yuan Ming Huang
Keyword(s):  
Phase Transition ◽  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
Liquid Crystals ◽  
Optical Microscopy ◽  
Scanning Calorimetry ◽  
Polarized Optical Microscopy ◽  
Phase Transition Temperatures ◽  
Second Category ◽  
Mesomorphic Properties

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.

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
Keyword(s):  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
Liquid Crystals ◽  
Optical Microscopy ◽  
Liquid Crystalline ◽  
Benzoic Acids ◽  
Scanning Calorimetry ◽  
Polarized Optical Microscopy ◽  
Acyl Chlorides ◽  
Esterification Reactions

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.

Dependence of Phase Transition of a Bent-Core Liquid Crystal on the Heating Rate

2010 ◽  
Vol 663-665 ◽  
pp. 787-790 ◽  
Author(s):  
Qing Lan Ma ◽  
Yuan Ming Huang
Keyword(s):  
Phase Transition ◽  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
Optical Microscopy ◽  
Heating Rate ◽  
Broad Peak ◽  
Crystal Phase ◽  
Scanning Calorimetry ◽  
Polarized Optical Microscopy ◽  
Crystal Compound

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.

Influence of Cooling Rates on Phase Transitions of Bent-Core Liquid Crystal 1,3-Phenylene-bis[4-(hexylcarboyloxyl)benzylideneamine]

2010 ◽  
Vol 428-429 ◽  
pp. 247-250 ◽  
Author(s):  
Yuan Ming Huang ◽  
Qing Lan Ma ◽  
Bao Gai Zhai
Keyword(s):  
Differential Scanning Calorimetry ◽  
Phase Transitions ◽  
Liquid Crystal ◽  
Optical Microscopy ◽  
Cooling Rate ◽  
Scanning Calorimetry ◽  
Slow Cooling ◽  
Cooling Rates ◽  
Polarized Optical Microscopy ◽  
Fast Cooling

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.

Deep-Blue Photoluminescent Properties of a Liquid Crystal TB10A

2011 ◽  
Vol 181-182 ◽  
pp. 33-38 ◽  
Author(s):  
Qing Lan Ma ◽  
Rui Xiong ◽  
Yuan Ming Huang
Keyword(s):  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
Electronic Structures ◽  
Room Temperature ◽  
Tight Binding ◽  
Electronic Structure Calculations ◽  
Scanning Calorimetry ◽  
Deep Blue ◽  
Tight Binding Method ◽  
Structure Calculations

A typical liquid crystal (LC) N,N-(terephthalylidene) bis (4-decylbenzenamine) (TB10A) was firstly synthesized at room temperature. The synthesized LC TB10A were investigated by differential scanning calorimetry (DSC), polarizing optical microscopy (POM), ultraviolet-visible (UV-vis) spectrophotometry, photoluminecence (PL) spectroscopy and electronic structure calculations. Upon the 325 nm excitation, the dilute tetrahydrofuran solutions of TB10A could give off blue PL. With Hückel tight-binding method, the electronic structures of the TB10A were calculated. Our results demonstrated that the deep-blue PL observed at about 489 nm (2.54 eV) can be assigned to theπ* →ntransition for the TB10A.

Mesophase Studies and Charge Transportation Properties of 3,6-dicarbethoxy-2,7,10,11-tetra-pentyloxytriphenylene

2011 ◽  
Vol 181-182 ◽  
pp. 193-196
Author(s):  
Chun Xiu Zhang ◽  
Jia Ling Pu ◽  
Hao Wu ◽  
Ao Zhang ◽  
Ming Xia Zhang ◽  
...  
Keyword(s):  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
Optical Microscopy ◽  
Chemical Structure ◽  
Room Temperature ◽  
Time Of Flight ◽  
Scanning Calorimetry ◽  
Columnar Phase ◽  
Discotic Liquid Crystal ◽  
Time Of Flight Method

In this study, a triphenylene-based discotic liquid crystal 3,6-dicarbethoxy-2,7,10,11-tetra-pentyloxytriphenylene was synthesized. The chemical structure was characterized by FTIR, 1HNMR.The mesophases of the material synthesized here was characterized by using polarizing optical microscopy (POM), differential scanning calorimetry (DSC). It was found that the compound displayed columnar phase during cooling at 164.7 °C and the columnar phase can be preserved even at room temperature. The charge transportation properties of the compound were measured by using time-of-flight method.

Synthesis and Mesomorphism of Semi-Fluorinated Chain Liquid Crystals with [1,2,3]-Triazole Rings

2010 ◽  
Vol 428-429 ◽  
pp. 135-139
Author(s):  
Yang Yang ◽  
Ke Qing Zhao ◽  
Wen Hao Yu ◽  
Bi Qin Wang ◽  
Ping Hu
Keyword(s):  
Differential Scanning Calorimetry ◽  
Liquid Crystals ◽  
Optical Microscopy ◽  
Cycloaddition Reaction ◽  
Scanning Calorimetry ◽  
Smectic A ◽  
Smectic A Phase

Series of semi-fluorinated chain liquid crystals with [1,2,3]-triazole rings have been synthesized with CuI-Et3N catalyzed alkyne-azide cycloaddition reaction. The selectively produced 1,4-disubstituted regioisomers were characterized by using IR, NMR, and Mass. The mesomorphic behaviors were characterized with polarizing optical microscopy and differential scanning calorimetry. Compounds with perfluorinated chains have showed smectic A phase.

Synthesis and Properties of Novel Thiophene-Based Liquid Crystalline Conducting Polymers

2017 ◽  
Vol 25 (9) ◽  
pp. 669-676 ◽  
Author(s):  
Danesh Roudini
Keyword(s):  
Magnetic Field ◽  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
Optical Microscopy ◽  
Electronic Properties ◽  
Liquid Crystalline ◽  
Side Chain ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Crystal Properties

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.

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