The effect of structural changes in the molecular core and periphery on the liquid-crystalline properties of some chiral 4-n-alkoxyphenylpropiolates

1992 ◽  
Vol 11 (1) ◽  
pp. 135-143 ◽  
Author(s):  
M. A. Waugh ◽  
S. M. Stein ◽  
E. Chin ◽  
J. W. Goodby
2006 ◽  
Vol 33 (10) ◽  
pp. 1143-1151 ◽  
Author(s):  
Ewa BiaŁecka‐Florjańczyk ◽  
Ewa Majewska ◽  
Dorota Melon‐Ksyta ◽  
Irma Śledzińska ◽  
Jan Przedmojski ◽  
...  

2021 ◽  
Author(s):  
Adam Milsom ◽  
Adam M. Squires ◽  
Jacob A. Boswell ◽  
Nicholas J. Terrill ◽  
Andrew D. Ward ◽  
...  

Abstract. Organic aerosols are key components of the Earth’s atmospheric system. The phase state of organic aerosols is known to be a significant factor in determining aerosol reactivity, water uptake and atmospheric lifetime – with wide implications for cloud formation, climate, air quality and human health. Unsaturated fatty acids contribute to urban cooking emissions and sea spray aerosols. These compounds, exemplified by oleic acid and its sodium salt, are surface active and have been shown to self-assemble into a variety of liquid-crystalline phases upon addition of water. Here we observe a crystalline acid–soap complex in acoustically levitated oleic acid–sodium oleate particles. We developed a synchrotron-based simultaneous Small-Angle & Wide-Angle X-ray Scattering (SAXS/WAXS)/Raman microscopy system to probe physical and chemical changes in the proxy during exposure to humidity and the atmospheric oxidant ozone. We present a spatially resolved structural picture of a levitated particle during humidification, revealing a phase gradient consisting of a disordered liquid crystalline shell and crystalline core. Ozonolysis is significantly slower in the crystalline phase compared with the liquid phase and a significant portion (34 ± 8 %) of unreacted material remains after extensive oxidation. We present experimental evidence of inert surface layer formation during ozonolysis, taking advantage of spatially resolved simultaneous SAXS/WAXS experiments. These observations suggest atmospheric lifetimes of surface-active organic species in aerosols are highly phase dependent, potentially impacting on climate, urban air quality and long-range transport of pollutants such as Polycyclic Aromatic Hydrocarbons (PAHs).


2005 ◽  
Vol 32 (5) ◽  
pp. 565-572 ◽  
Author(s):  
M. Garić ◽  
A. Bubnov ◽  
V. Novotná ◽  
M. Kašpar ◽  
V. Hamplová ◽  
...  

1999 ◽  
Vol 46 (4) ◽  
pp. 841-851 ◽  
Author(s):  
B Piekarska ◽  
J Rybarska ◽  
B Stopa ◽  
G Zemanek ◽  
M Król ◽  
...  

Congo red and a group of structurally related dyes long used to stain amyloid proteins are known to associate in water solutions. The self-association of some dyes belonging to this group appears particularly strong. In water solutions their molecules are arranged in ribbon-like micellar forms with liquid crystalline properties. These compounds have recently been found to form complexes with some native proteins in a non-standard way. Gaps formed by the local distribution of beta-sheets in proteins probably represent the receptor sites for these dye ligands. They may result from higher structural instability in unfolding conditions, but also may appear as long range cooperative fluctuations generated by ligand binding. Immunoglobulins G were chosen as model binding proteins to check the mechanism of binding of these dyes. The sites of structural changes generated by antigen binding in antibodies, believed to act as a signal propagated to distant parts of the molecule, were assumed to be suitable sites for the complexation of liquid-crystalline dyes. This assumption was confirmed by proving that antibodies engaged in immune complexation really do bind these dyes; as expected, this binding affects their function by significantly enhancing antigen binding and simultaneously inhibiting C1q attachment. Binding of these supramolecular dyes by some other native proteins including serpins and their natural complexes was also shown. The strict dependence of the ligation properties on strong self-assembling and the particular arrangement of dye molecules indicate that supramolecularity is the feature that creates non-standard protein ligands, with potential uses in medicine and experimental science.


Nanoscale ◽  
2020 ◽  
Vol 12 (21) ◽  
pp. 11468-11479
Author(s):  
Satoshi Kajiyama ◽  
Hiroki Iwase ◽  
Masanari Nakayama ◽  
Rino Ichikawa ◽  
Daisuke Yamaguchi ◽  
...  

The shear-induced structural changes and phase transition behaviour of colloidal hydroxyapatite-based nanorod composites are examined using in situ small-angle neutron scattering and rheological measurements.


1985 ◽  
Vol 40 (7) ◽  
pp. 981-986 ◽  
Author(s):  
Bernd Kohne ◽  
Klaus Praefcke ◽  
Werner Stephan ◽  
Peter Nürnberg

Abstract A modified synthesis of mytilitol and the synthesis of various esters of the cyclitols myo-inositol (la) and mytilitol (2a) is described. Because of steric reasons all these derivatives of the two naturally occuring compounds exhibit no discotic mesophases. For instance, in comparison to mesomorphous scyllitol hexaesters already the methyl group perpendicular to the molecular core in the analogous hexaesters 2b-d of mytilitol suppresses discotic liquid crystalline character totally. This effect is discussed in connection to the relationship of mesomorphism with chemical structure of disc-shaped molecules.


1996 ◽  
Vol 51 (9) ◽  
pp. 1019-1026 ◽  
Author(s):  
S. Heinemann ◽  
H. Kresse ◽  
S. Saito ◽  
D. Demus

Abstract Measurements of the temperature and frequency dependence of dielectric constants have been performed for five homologues in the range 100 Hz -10 MHz. These substances exhibit a negative anisotropy of the dielectric constants and two relaxation regions (rotation of the molecules around the short resp. long axis) in the investigated frequency range. Even in the crystalline state dipolar reorientations are possible which have been interpreted as rotations of the alkoxy group. Changes of the static dielectric constants, relaxation frequencies and transition entropies are discussed as a measure of structural changes passing the several liquid crystalline phases.


2004 ◽  
Vol 31 (6) ◽  
pp. 821-830 ◽  
Author(s):  
Miroslav Kašpar ◽  
Alexej Bubnov ◽  
Věra Hamplová ◽  
Slavomír Pirkl ◽  
Milada Glogarová

2008 ◽  
Vol 22 (1) ◽  
pp. 33-41 ◽  
Author(s):  
Danuta Pentak ◽  
Wiesław W. Sułkowski ◽  
Agnieszka Wolińska ◽  
Sławomir Maślanka ◽  
Barbara Bojko ◽  
...  

The EPR spectroscopy was used to determine the structure and physicochemical properties of liposomes prepared from L-α-phosphatidylcholine dipalmitoyl (DPPC) by the modified reverse-phase evaporation method (mREV). EPR study was carried out in the temperature range from 297 K to 340 K i.e. below and above the phase transition temperatureTCof DPPC. On the basis of EPR spectra of spin marker 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) incorporated into the liposome, the parameterfwas determined. TEMPO dissolves easily in water and in the fluid lamellar smectic liquid-crystaline phase of lipid bilayer but is largely excluded from the solid, gel-phase. Thus TEMPO can be used to observe the change in the partition between aqueous and fluid lipid regions. The change in the relative value offas a function of temperature for DPPC shows that, in the presence of water excess, this phospholipids undergoes a transition from a “gel phase” to a lamellar smectic liquid crystalline phase. On the basis of EPR spectra of spin marker 2-(3carboxypropyl)-4,4-dimethyl-2-tridecyl-3-oxazolidinloxyl (5-DOXYL) incorporated into liposome, the parametera'Nwas determined. The isotropic14N-hyperfine coupling constanta'Nof nitroxide spin label depends on the local environmental polarity. The increase ofa'Nvalue reflects the rise of polarity of spin label environment. Temperature, cholesterol and pH dependent structural changes were also described.


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