Thermal relaxation model of surface director gliding in lyotropic liquid crystals

1997 ◽  
Vol 55 (4) ◽  
pp. 4314-4320 ◽  
Author(s):  
P. Galatola ◽  
G. Barbero ◽  
A. K. Zvezdin
2021 ◽  
Author(s):  
Max Hirschmann ◽  
Christina M. Thiele

<p><b>In nature, proteins like rhodopsin act as transducer for photo-chemical reactions causing biological responses (e.g. enabling vision)</b><b>. The underlying concept – a photo-induced conformational change of the protein as amplifier of the photo-responsive moiety – can also be adopted by synthetical polymers or foldamers</b><b> </b><b>that have the propensity to form ordered secondary structures (e.g. polypeptides)</b><b>. An alternative approach to amplify photo-chemical responses is their incorporation into liquid crystals</b><b>. With only a few exceptions</b><b>, photo-insensitive liquid crystals are doped with dyes</b><b> </b><b>that favour disorder upon irradiation</b><b>. In theory, photo-responsive polypeptides</b><b>, capable of forming lyotropic liquid crystals</b><b>, could exploit both amplification approaches but, in practice, their photo-responsivity is hampered by the reduced mobility of polypeptides in concentrated solutions</b><b>. Here we show that the E/Z photo-isomerisation of an azobenzene containing polyaspartate initiates a helix-coil backbone transition, which reversibly alters the polypeptide solution from anisotropic to isotropic. In contrast to other photo-responsible polymers</b><b>14</b><b>, in which thermal relaxation to the more stable photo-isomer is quite fast, both photo-isomers are thermally stable and interconvertible by visible light in a single solvent. Local irradiation and magnetic fields lead to spatial resolution and unidirectional architectures of the liquid crystal, respectively. Our results demonstrate that photo-isomerisation on a molecular level is amplified in three stages via intra- and intermolecular interactions to yield a unidirectional, chiral liquid crystal. We believe, the morphological changes of the liquid crystal induced by light will facilitate a multitude of applications, like photo-alignment</b><b> </b><b>or the photo-control of solution viscosity</b><b> </b><b>and anisotropic </b><br></p> <p><b>diffusion</b><b>. When incorporated into layer-by-layer architectures the polymer could find application in biomedicine</b><b> </b><b>and the spatial and temporal resolution could be exploited in nano-technology</b><b>. </b></p>


2021 ◽  
Author(s):  
Max Hirschmann ◽  
Christina M. Thiele

<p><b>In nature, proteins like rhodopsin act as transducer for photo-chemical reactions causing biological responses (e.g. enabling vision)</b><b>. The underlying concept – a photo-induced conformational change of the protein as amplifier of the photo-responsive moiety – can also be adopted by synthetical polymers or foldamers</b><b> </b><b>that have the propensity to form ordered secondary structures (e.g. polypeptides)</b><b>. An alternative approach to amplify photo-chemical responses is their incorporation into liquid crystals</b><b>. With only a few exceptions</b><b>, photo-insensitive liquid crystals are doped with dyes</b><b> </b><b>that favour disorder upon irradiation</b><b>. In theory, photo-responsive polypeptides</b><b>, capable of forming lyotropic liquid crystals</b><b>, could exploit both amplification approaches but, in practice, their photo-responsivity is hampered by the reduced mobility of polypeptides in concentrated solutions</b><b>. Here we show that the E/Z photo-isomerisation of an azobenzene containing polyaspartate initiates a helix-coil backbone transition, which reversibly alters the polypeptide solution from anisotropic to isotropic. In contrast to other photo-responsible polymers</b><b>14</b><b>, in which thermal relaxation to the more stable photo-isomer is quite fast, both photo-isomers are thermally stable and interconvertible by visible light in a single solvent. Local irradiation and magnetic fields lead to spatial resolution and unidirectional architectures of the liquid crystal, respectively. Our results demonstrate that photo-isomerisation on a molecular level is amplified in three stages via intra- and intermolecular interactions to yield a unidirectional, chiral liquid crystal. We believe, the morphological changes of the liquid crystal induced by light will facilitate a multitude of applications, like photo-alignment</b><b> </b><b>or the photo-control of solution viscosity</b><b> </b><b>and anisotropic </b><br></p> <p><b>diffusion</b><b>. When incorporated into layer-by-layer architectures the polymer could find application in biomedicine</b><b> </b><b>and the spatial and temporal resolution could be exploited in nano-technology</b><b>. </b></p>


1984 ◽  
Vol 45 (2) ◽  
pp. 273-281 ◽  
Author(s):  
M.B. Schneider ◽  
W.W. Webb

2017 ◽  
Vol 121 (19) ◽  
pp. 5048-5057 ◽  
Author(s):  
Jesse G. McDaniel ◽  
Arun Yethiraj

1980 ◽  
Vol 28 (18) ◽  
pp. 608-612 ◽  
Author(s):  
D. Senatra ◽  
M. Vannini ◽  
A. P. Neri

Author(s):  
Kang Wang ◽  
Zhi Li ◽  
Yiming Huang ◽  
YaotianTao ◽  
Xiao Liang ◽  
...  

Soft Matter ◽  
2021 ◽  
Author(s):  
Peng Bao ◽  
Daniel A. Paterson ◽  
Sally A. Peyman ◽  
J. Cliff Jones ◽  
Jonathan A. T. Sandoe ◽  
...  

We describe a modified microfluidic method for making Giant Unilamellar Vesicles (GUVs) via water/octanol-lipid/water double emulsion droplets and encapsulation of nematic lyotropic liquid crystals (LNLCs).


1999 ◽  
Vol 102 (3) ◽  
pp. 221-226
Author(s):  
Yueying Gao ◽  
Xiaoqin Xia

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