Structures and properties of cholesteric liquid crystalline elastomers

2005 ◽  
Vol 63 (1) ◽  
pp. 55-61 ◽  
Author(s):  
Ying-Gang Jia ◽  
Bao-Yan Zhang ◽  
Mei Tian ◽  
Ke-Qi Wei
2003 ◽  
Vol 35 (2) ◽  
pp. 160-166 ◽  
Author(s):  
Jian-She Hu ◽  
Bao-Yan Zhang ◽  
Ying-Gang Jia ◽  
Ying Wang

2003 ◽  
Vol 36 (24) ◽  
pp. 9060-9066 ◽  
Author(s):  
Jian-She Hu ◽  
Bao-Yan Zhang ◽  
Ying-Gang Jia ◽  
Song Chen

2021 ◽  
Author(s):  
Tetyana Koso ◽  
Marco Beaumont ◽  
Blaise Tardy ◽  
Daniel Rico del Cerro ◽  
Samuel Eyley ◽  
...  

Gas-phase acylation of cellulose is an attractive method for modifying the surface properties of cellulosics. However, little is known concerning the regioselectivity of the chemistry, in terms of which cellulose positions are preferentially acylated and if acylation can be restricted to the surface, preserving crystallinities/morphologies. Consequently, we reexplore simple gas-phase acetylation of modern-day cellulosic building blocks – cellulose nanocrystals, pulps, regenerated fibre and aerogels. The gas-phase acetylation is shown to be highly regioselective for the C6-OH, is further supported with computational modelling. This contrasts with liquid-state acetylation, highlighting that the gas-phase chemistry is much more controllable, yet with similar kinetics to the uncatalyzed liquid-phase reactions. Furthermore, this method preserves both the native crystalline structure of cellulose and the supramolecular morphologies of even delicate cellulosic constructs (aerogel exhibiting retention of chiral cholesteric liquid crystalline phases). Therefore, we are convinced that this methodology will lead to more rapid adoption of precisely tailored and cellulosic materials


2014 ◽  
Vol 26 (29) ◽  
pp. 4919-4919 ◽  
Author(s):  
Yoshiaki Uchida ◽  
Yoichi Takanishi ◽  
Jun Yamamoto

1979 ◽  
Vol 57 (4) ◽  
pp. 458-465 ◽  
Author(s):  
Robert J. Cushley ◽  
Bruce J. Forrest ◽  
Anne Gillis ◽  
Jenifer Tribe

Phospholipid bilayers containing branched chain molecules, phytol (1), vitamin E (2), and phytanic acid (3), have been investigated by 31P nmr, esr, and differential scanning calorimetry (dsc).A 31P lanthanide induced shift study indicated varying permeabilities to Pr3+ in the order phytanic acid > vitamin E > phytol > egg yolk lecithin alone; the half-lives (in days) were 0.002, 0.14, 0.83, and 6.5, respectively. The activation energy for Pr3+ permeation through the egg yolk lecithin–phytol membrane was found to be 84.9 ± 0.8 kJ.The following esr order parameters, S3, were obtained using the extrinsic spin label, 5-doxylpalmitic acid, in oriented mixed multibilayers: S3 (1) = 0.29, S3 (2) = 0.50, and S3 (3) = 0.02.Differential scanning calorimetry revealed a lowering of the gel–liquid crystalline phase transition temperature, Tc, as the concentration of incorporated isoprenoid compound increases, with eventual disappearance of the endotherm. Specific entropy, s, calculated for dipalmitoyl lecithin +25 mol% 3 is 126 J kg−1 K−1 compared to s = 114.2 J kg−1 K−1 for 1and s = 85 J kg−1 K−1 for 2.


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