Blue Light Emission from a Rod-Like Liquid Crystal

2010 ◽  
Vol 428-429 ◽  
pp. 288-291 ◽  
Author(s):  
Bao Gai Zhai ◽  
Yuan Ming Huang
Keyword(s):  
Liquid Crystal ◽  
Liquid Crystalline ◽  
Light Emission ◽  
Tight Binding ◽  
Resonance Spectroscopy ◽  
Scanning Calorimetry ◽  
Blue Light Emission ◽  
Liquid Crystalline Phases ◽  
Dominant Peak ◽  
Blue Photoluminescence

A rod-like liquid crystal 4-butoxybenzylidene-4'-octylphenylamine was synthesized. The molecular structure and the liquid crystalline phases of the synthesized compound were characterized with the nuclear magnetic resonance spectroscopy, the differential scanning calorimetry, and the polarizing optical microscopy, respectively. The absorption measurement shows that the dilute tetrahydrofuran solutions of the rod-like liquid crystal absorb photons at about 290 and 330 nm, respectively; while the luminescence measurements indicate that this rod-like liquid crystal can give off intense blue photoluminescence with its dominant peak located at about 430 nm. Using Hückel tight-binding program, we have calculated the electronic structures of the liquid crystal, and the origin of the blue photoluminescence is discussed. Introduction

Electron microscopy and diffraction of crystalline dendrimers and macrocycles

1993 ◽  
Vol 51 ◽  
pp. 1218-1219
Author(s):  
C. J. Buchko ◽  
P. M. Wilson ◽  
Z. Xu ◽  
J. Zhang ◽  
S. Lee ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Liquid Crystalline ◽  
Structural Information ◽  
High Resolution Electron Microscopy ◽  
Scanning Calorimetry ◽  
Tertiary Butyl ◽  
Phenyl Acetylene ◽  
Selected Area Electron Diffraction ◽  
Liquid Crystalline Phases ◽  
Resolution Electron

The synthesis of well-defined organic molecules with unique geometries opens new opportunities for understanding and controlling the organization of condensed matter. Here, we study dendrimers and macrocycles which are synthesized from rigid phenyl-acetylene spacer units, Both units are solubilized by the presence of tertiary butyl groups located at the periphery of the molecule. These hydrocarbon materials form crystalline and liquid crystalline phases which have been studied by differential scanning calorimetry, hot stage optical microscopy, and wide-angle x-ray scattering (WAXS).The precisely defined architecture of these molecules makes it possible to investigate systematic variations in chemical architecture on the nature of microstructural organization. Here we report on the transmission electron microscopy (TEM), selected area electron diffraction (SAED), and high resolution electron microscopy (HREM) studies of crystalline thin films formed by deposition of these materials onto carbon substrates from dilute solution. Electron microscopy is very attractive for gaining structural information on new molecules due to the scarcity of material to grow single crystals suitable for conventional crystallography.

Characterization of some mesogenic alkyl 1-thioglycosides

2002 ◽  
Vol 80 (8) ◽  
pp. 1162-1165 ◽  
Author(s):  
B Henrissat ◽  
G K Hamer ◽  
M G Taylor ◽  
R H Marchessault
Keyword(s):  
Phase Transition ◽  
Liquid Crystal ◽  
Solid State ◽  
Solid State Nmr ◽  
Liquid Crystalline ◽  
Liquid Crystal Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Liquid Crystalline Phases

A series of dodecyl 1-thio-β-D-glycosides has been synthesized and characterized (DSC, NMR, CP MAS, X-ray diffraction) as possible new marking materials with liquid-crystalline properties. These compounds undergo solid to liquid crystal phase transitions at various temperatures, which depend on the nature of the carbohydrate part of the structure. Their liquid-crystalline phases show extreme shear thinning behaviour.Key words: liquid crystal, powder X-ray diffraction, phase transition, thioglycoside, solid-state NMR, marking material

Inosose-Flüssigkristalle / Inosose Liquid Crystals

1990 ◽  
Vol 45 (7) ◽  
pp. 1084-1090 ◽  
Author(s):  
Klaus Praefcke ◽  
Bernd Kohne ◽  
Andreas Eckert ◽  
Joachim Hempel
Keyword(s):  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
High Temperature ◽  
Liquid Crystalline ◽  
Structural Features ◽  
Lyotropic Liquid Crystal ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Alkyl Chains

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.

scholarly journals Mesomorphism behaviour and photoluminescent properties of new asymmetrical 1,2-di(4-alkoxybenzylidene)hydrazines

2019 ◽  
Vol 43 (1-2) ◽  
pp. 67-77 ◽  
Author(s):  
Adil A Awad ◽  
Al-Ameen Bariz OmarAli ◽  
Ahmed Jasim M Al-Karawi ◽  
Zyad Hussein J Al-Qaisi ◽  
Samer Ghanim Majeed
Keyword(s):  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
Liquid Crystalline ◽  
Polarized Light ◽  
Luminescent Properties ◽  
Scanning Calorimetry ◽  
Crystalline Materials ◽  
X Ray ◽  
Step Procedure ◽  
Liquid Crystalline Materials

{1-[4-( n-Alkoxy)]-2-(4’-decyloxy)benzylidene}hydrazines ( n-alkoxy = O(CH2) nH, n = 1–9, 12, 16 or 18), an asymmetrical series of 1,2-disubstituted hydrazines, were prepared in a simple two-step procedure as a part of our continuing work in evaluating hydrophobic azine compounds as photoluminescent liquid crystalline materials. The compounds were characterized spectroscopically and their liquid crystalline behaviour and luminescent properties were evaluated using polarized light optical microscopy, differential scanning calorimetry and X-ray powder diffraction techniques. The studies revealed that all of these compounds are liquid crystalline materials exhibiting photoluminescent properties in the crystalline and liquid crystal states.

Synthesis of Segmented Anisotropic-Isotropic Poly(Aryl Ester)Poly(Arylene Ether) Copolymers

1989 ◽  
Vol 175 ◽  
Author(s):  
J. E. McGratn ◽  
K. L. Cooper ◽  
W. Waehamad ◽  
H. Huang ◽  
G. L. Wilkes
Keyword(s):  
Molecular Weight ◽  
Liquid Crystal ◽  
Benzoic Acid ◽  
Liquid Crystalline ◽  
Average Molecular Weight ◽  
Nucleophilic Aromatic Substitution ◽  
Copolymer Composition ◽  
Aromatic Substitution ◽  
Scanning Calorimetry ◽  
Arylene Ether

AbstractCarboxyl functional poly(arylene ether) oligomers of controlled number average molecular weight were synthesized via nucleophilic aromatic substitution step polymerization using p-hydroxy benzoic acid as the molecular weight and end group controlling reagents. The subsequent functionalized polyarylene ethers were copolymerized with acetoxy benzoic acid or acetoxyphenoxy benzoic acid via melt acidolysis procedures. Successful copolymers were generated using chlorobenzene as a solvent for the first s age of the reaction followed by melt reaction at temperatures as high as 325°C. Resulting copolymer composition and segment size were investigated. It was possible to prepare improved solvent resistant copolymers through incorporation of the liquid crystal polyester (LCP) segment. Extraction tests using boiling chloroform showed that a high percentage of segmented copolymer were generated. Swelling characteristics were also noted and were observed to decrease as a function of the LCP concentration utilized. Multiple transitions were observed in differential scanning calorimetry consistent with Tg's, Tm's and possibly with liquid crystal transitions. Optical microscopy showed an ordered microstructure developed which is consistent with the presence of liquid crystalline phases. The materials were successfully compression molded to afford tough coherent films at all compositions, implying the likelihood of improved compressive strength relative to the LCP homo- or copolyesters.

Synthesis and Characterization of Stilbene Derivatives for Possible Incorporation as Smart Additives in Polymers Used as Packaging Films.

1997 ◽  
Vol 50 (4) ◽  
pp. 425 ◽  
Author(s):  
Gary M. Day ◽  
Owen T. Howell ◽  
Michael R. Metzler ◽  
Paul D. Woodgate
Keyword(s):  
Differential Scanning Calorimetry ◽  
Liquid Crystalline ◽  
Synthesis And Characterization ◽  
Scanning Calorimetry ◽  
Packaging Films ◽  
Multiple Phase ◽  
Liquid Crystalline Phases ◽  
Crystal Properties ◽  
Stilbene Derivatives

Several series of stilbene derivatives for possible use as smart additives in polymers used as packaging films have been prepared and characterized. Differential scanning calorimetry was performed on some of the stilbenes in order to determine any liquid crystal properties. Those compounds which had multiple phase transitions were also shown to have two liquid crystalline phases according to optical microscopy.

Study of the Liquid Crystalline Phases in Some Compounds of 4-Trans-(4-Alkyl)Cyclo-Hexylphenyl-Alkylcarboxylate

1983 ◽  
Vol 38 (12) ◽  
pp. 1362-1364 ◽  
Author(s):  
I. H. Ibrahim ◽  
W. Haase
Keyword(s):  
Differential Scanning Calorimetry ◽  
Nematic Phase ◽  
Liquid Crystalline ◽  
Intermolecular Distance ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Enthalpy Changes ◽  
Liquid Crystalline Phases ◽  
Nematic Phases

Abstract Three mesogenic compounds of the general formula have been investigated by differential scanning calorimetry. thermal optical microscopy and X-ray diffraction methods/Enthalpy changes of The different phase transitions for these compounds have been determined. H33 exhibits smectic B and nematic phases, whereas H34 and H75 exhibit only smectic B phases. The thickness of the smectic layers and the average intermolecular distance have been evaluated, as well as the corresponding molecular parameters in the nematic phase.

scholarly journals Cubic and tetragonal liquid crystal phases composed of non-chiral molecules: Chirality and macroscopic properties

2019 ◽  
Vol 42 (11) ◽  
Author(s):  
Helmut R. Brand ◽  
Harald Pleiner
Keyword(s):  
Liquid Crystal ◽  
Liquid Crystalline ◽  
Triblock Copolymers ◽  
Similar Type ◽  
Chiral Molecules ◽  
Chiral Compounds ◽  
Liquid Crystalline Phases ◽  
Symmetry Properties ◽  
Crystal Phases ◽  
Liquid Crystal Phases

Abstract. We discuss the symmetry properties as well as the macroscopic behavior of the cubic liquid crystal phases showing large chiral domains of either hand in some non-chiral compounds reported recently in the group of Tschierske. These phases are tricontinuous. While they have O or I432 symmetry in each chiral domain, the overall symmetry is $ I m \bar{3} m$Im3¯m as there is no net chirality for compounds composed of non-chiral molecules. It turns out that a rather similar type of phase has also been reported for triblock copolymers. Here we analyze in detail the macroscopic static and dynamic behavior of such phases and we predict, among other results, that they show the analog of static and dissipative Lehmann-type effects in their chiral domains. A description of a cubic liquid crystalline phase of Th symmetry, which has not yet been found experimentally, is also included. Suggestions for experiments are outlined to identify such a phase. In addition, we discuss tetragonal liquid crystalline phases of D4h and D4 (I422) symmetry as they have been reported last year experimentally in connection to the Q phase. Graphical abstract

Chiral Liquid Crystalline Polymers Containing Isosorbide Groups

2013 ◽  
Vol 781-784 ◽  
pp. 403-406
Author(s):  
Mei Tian ◽  
Zhi Xin Xu ◽  
Li Gao ◽  
Dan Shu Yao ◽  
Xiao Zhi He ◽  
...  
Keyword(s):  
Liquid Crystal ◽  
Liquid Crystalline ◽  
Main Chain ◽  
Liquid Crystalline Polymers ◽  
Optical Microscope ◽  
Liquid Crystal Polymers ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Crystalline Polymers

A series of new main-chain liquid-crystal polymers (LCPs) were prepared from sebacoyl chloride (SD) and various amount of 4, 4-Dihydroxy-2, 2-dimethyl Benzalazine (DDBA) and isosorbide (ISO). The liquid crystal (LC) properties were investigated by polarized optical microscope (POM), differential scanning calorimetry (DSC) and X-ray diffraction measurements. P1 exhibited a typical nematic thread texture, which contains no ISO. P2-P7 are Sc* and N LCPs, which exhibited broken fan-shaped texture and droplet texture. The introduction of chiral units into the polymers led to a change of mesomorphase, as compared with P1.

A new family of bent-core C2-symmetric liquid crystals

2010 ◽  
Vol 88 (7) ◽  
pp. 639-645 ◽  
Author(s):  
Kyle A. Hope-Ross ◽  
Paul A. Heiney ◽  
John F. Kadla
Keyword(s):  
Differential Scanning Calorimetry ◽  
Small Angle ◽  
Liquid Crystalline ◽  
Side Chains ◽  
Scanning Calorimetry ◽  
X Ray ◽  
New Family ◽  
X Ray Scattering ◽  
Factors Influencing ◽  
Liquid Crystalline Phases

A series of C2-symmetric compounds with different core sizes and varying lengths and numbers of alkoxy side chains were prepared, and the factors influencing their liquid crystalline mesophase behaviour were investigated. The compounds studied were based on benzophenone, dibenzylidene-acetone, and 1,9-diphenyl-nona-1,3,6,8-tetraen-5-one cores with either 1 or 2 linear alkoxy side chains. The side chains were varied in length from C6H13 to C12H25. The liquid crystalline mesophase behaviour of the compounds was investigated using differential scanning calorimetry, polarizing optical microscopy, and small-angle X-ray scattering (SAXS). It was found that a number of the molecules were able to self-assemble into smectic and nematic liquid crystalline phases.

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