Molecular Networks Forming Crystalline and Liquid Crystalline Phases by Combined Hydrogen-Bonding and Ionic Interactions

2004 ◽  
Vol 69 (5) ◽  
pp. 1161-1168 ◽  
Author(s):  
Mir Wais Hosseini ◽  
Dimitris Tsiourvas ◽  
Jean-Marc Planeix ◽  
Zili Sideratou ◽  
Nicolas Thomas ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Liquid Crystalline ◽  
Molecular Networks ◽  
Ionic Interactions ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Alkyl Chains ◽  
Smectic Phases ◽  
Liquid Crystalline Phases ◽  
Supramolecular Networks

Molecular recognition of cyclic bisamidinium dication with a series of 4-alkoxybenzoates afforded materials exhibiting lamellar crystalline structures at low temperatures and highly ordered smectic phases at higher temperatures. The liquid crystalline behaviour was investigated by differential scanning calorimetry, polarized optical microscopy and established by X-ray diffraction. Combined hydrogen-bonding and ionic interactions resulted in supramolecular networks which have sufficient stability to maintain their structure at high temperatures following the melting of the long alkyl chains.

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.

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 Liquid Crystalline Compounds in the Thiophene Series, Part 6+ Synthesis and Characterization of Azomethines and Vinylenes with Two Mesogenic Groups and Different Alkylene Spacer Lengths

1993 ◽  
Vol 48 (6) ◽  
pp. 826-843 ◽  
Author(s):  
Gerhard Koßmehl ◽  
Frank Dirk Hoppe ◽  
Barbara Hirsch
Keyword(s):  
Aromatic Amines ◽  
Liquid Crystalline ◽  
Synthesis And Characterization ◽  
Scanning Calorimetry ◽  
Polarizing Microscopy ◽  
Alkyl Chains ◽  
Liquid Crystalline Phases ◽  
Smectic Mesophase ◽  
Methylene Groups

Compounds which have two mesogenic groups with and without terminal alkyl chains containing thiophene systems, were prepared from α.ω-bis(5-formyl-2-thienyl)alkanes (3a-3n) and various aromatic amines or 2-fluorenyl-Wittig-salt (10). The liquid crystalline properties of these compounds were characterized by differential scanning calorimetry (DSC) and polarizing microscopy. Only the series of α.ω-bis{5-[N-(4′-butyloxybiphenyl-4-yl)imino]formyl-2-thienyl}alkanes (7a-71) showed enantiotropic smectic and nematic mesophases. The series of E,E-α.ω-bis[5-(2-fluorenylvinyl)-2-thienyl]alkanes (8a-81) showed enantiotropic nematic mesophases for the compounds with 4 and 6 methylene groups, monotropic nematic mesophases for the compounds with 7—12 methylene groups and no liquid crystalline phases for compounds with 3, 5, 16 methylene groups in the connecting alkylene chain. In contrast to the compounds 8a-81, E-l-(5-butyl-2-thienyl)-2-(2-fluorenyl)ethylene has a smectic mesophase.

Liquid Crystalline Compounds in the Thiophene Series, Part 11+ Liquid Crystalline Thiophene Carboxylic Esters

1995 ◽  
Vol 50 (8) ◽  
pp. 1265-1274 ◽  
Author(s):  
Gerhard Koßmehl ◽  
Barbara Hirsch
Keyword(s):  
Liquid Crystalline ◽  
Polarized Light ◽  
Scanning Calorimetry ◽  
Crystalline Phases ◽  
H Nmr ◽  
Smectic Phases ◽  
Liquid Crystalline Phases ◽  
Nematic Phases ◽  
Optical Textures ◽  
Carboxylic Esters

The new series of ten 4,4'-bis(5-alkyl-2-thienylcarbonyloxy)azobenzenes (2a -2j) and ten 2,5-bis(5-alkyl-2-thienylcarbonyloxy)toluenes (3a -3j) were prepared. These, as yet unknown esters were characterized in relation to their structures by elemental analyses, IR, UV, 1H NMR spectra and MS. The azobenzene-esters 2a -2j which form liquid crystalline phases were studied by microscopy under polarized light and DSC (differential scanning calorimetry). Through the observation of the optical textures nematic phases were monitored. Only 2j has an additional smectic phase; 2h and 2i form monotropic smectic phases during cooling. The toluene-esters 3a -3j do not form liquid crystalline phases.

SYNTHESIS AND PROPERTIES OF GELATORS DERIVED FROM TETRAPHENYLETHYLENE AND GALLIC ACID WITH AGGREGATION-INDUCED EMISSION

2013 ◽  
Vol 01 (03) ◽  
pp. 1340007 ◽  
Author(s):  
MIAO LUO ◽  
XIE ZHOU ◽  
ZHENGUO CHI ◽  
CHUNPING MA ◽  
YI ZHANG ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Liquid Crystalline ◽  
Van Der Waals Interactions ◽  
Hydrogen Bonding Interaction ◽  
Scanning Calorimetry ◽  
Polarized Optical Microscopy ◽  
Fibrous Network ◽  
Liquid Crystalline Phases ◽  
Bonding Interaction ◽  
Thermoreversible Gelation

Two novel organogelators (TEG and TAG) based on tetraphenylethylene and 3,4,5-tris(dodecyloxy) benzoic acid were synthesized through ester bond and amido bond linkages, respectively. Compounds TEG and TAG were able to induce gelation in ethanol. Aggregation-induced enhanced emission was observed in these organogelator molecules, with increased fluorescence intensity from the solutions to the gels. The completely thermoreversible gelation occurred due to the aggregation of the organogelators. In the process, a fibrous network was formed by a combination of intermolecular hydrogen bonding, π–π stacking and van der Waals interactions. These phenomena were observed in the xerogels by field-emission scanning electron microscopy and Fourier-transform infrared spectroscopy. The results of differential scanning calorimetry and polarized optical microscopy indicated that compound TAG exhibited stable liquid crystalline phases over a wide temperature range. The linking groups have severe influence on the properties of the organogelators, which was mainly attributed to the hydrogen bonding interaction in compound TAG.

Synthesis and Characterization of Bowl-Shaped Liquid Crystals with a Core of Calix[6]arene

2011 ◽  
Vol 396-398 ◽  
pp. 2202-2205
Author(s):  
Dan Shu Yao ◽  
Feng Li ◽  
Hao Jie Wang ◽  
Xiao Yun Li ◽  
Mei Tian ◽  
...  
Keyword(s):  
Liquid Crystals ◽  
Liquid Crystalline ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Cholesteric Phase ◽  
Chemical Structures ◽  
Liquid Crystalline Phases ◽  
Clearing Temperature ◽  
Mesomorphic Properties

A new kind of bowl-shaped liquid crystals were designed and synthesized by esterification. They used a calix[6]arene as central unit and ω- cholesteric alkyl diacid monoester as mesogenic arms. Their chemical structures were confirmed by FTIR and 1HNMR spectra, their mesomorphic properties and phase behavior were investigated by differential scanning calorimetry (DSC), polarizing optical microscopy (POM) and X-Ray Diffraction (XRD) measurements. The results showed that the kind of calix[6]arene bowl-shaped liquid crystals N1-N3 exhibited broad range liquid crystalline phases at moderate temperature, and they displayed cholesteric phase focal-conic texture in liquid crystal states. With increasing the flexibility of monomers M1-M3, the melting point and the clearing temperature decreased in the macromolecules.

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

Liquid crystalline polyureas with oligo(ethylene glycol) sequences

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Shahram Mehdipour-Ataei ◽  
Leila Akbarian-Feizi
Keyword(s):  
Liquid Crystalline ◽  
Spectroscopic Method ◽  
Polymerization Reaction ◽  
X Ray Diffraction ◽  
Subsequent Reaction ◽  
Scanning Calorimetry ◽  
Polar Solvents ◽  
X Ray ◽  
H Nmr ◽  
Ft Ir

AbstractA diamine monomer containing ester, amide and ether functional groups was prepared and its polymerization reaction with different diisocyanates to give main chain poly(ester amide ether urea)s was investigated. The monomer was synthesized via reaction of terephthaloyl chloride with 4-hydroxybenzoic acid and subsequent reaction of the resulted diacid with 1,8-diamino-3,6-dioxaoctane. The polymers were characterized by FT-IR and 1H-NMR spectroscopic method and elemental analysis. The resulting polymers exhibited excellent solubility in polar solvents. Crystallinity of the resulted polymers was evaluated by wide-angle X-ray diffraction (WXRD) method, and they exhibited semi-crystalline patterns. The glass transition temperatures (Tg) of the polymers determined by differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) were in the range of 88-112 °C. The temperatures for 10% weight loss (T10) from their thermogravimetric analysis (TGA) curves were found to be in the range of 297-312 °C in air. Also the prepared polyureas showed liquid crystalline character.

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