A theory of the relative stabilities of the cubic phases of magnesium and calcium oxides

1996 ◽  
Vol 8 (30) ◽  
pp. 5509-5525 ◽  
Author(s):  
N C Pyper
1990 ◽  
Vol 51 (C7) ◽  
pp. C7-105-C7-108
Author(s):  
S. CRIBIER ◽  
L. BOURDIEU ◽  
R. VARGAS ◽  
A. GULIK ◽  
V. LUZZATI

1990 ◽  
Vol 51 (C7) ◽  
pp. C7-25-C7-34 ◽  
Author(s):  
P. BAROIS ◽  
D. EIDAM ◽  
S. T. HYDE
Keyword(s):  
X Ray ◽  

2000 ◽  
Vol 56 (s1) ◽  
pp. s83-s83
Author(s):  
P. Nollert ◽  
M. L. Chiu ◽  
M. C. Loewen ◽  
A. Royant ◽  
H. Behrhali ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Jie Liu ◽  
Wenzhe Liu ◽  
Bo Guan ◽  
Bo Wang ◽  
Lei Shi ◽  
...  

AbstractIn a narrow temperature window in going from the isotropic to highly chiral orders, cholesteric liquid crystals exhibit so-called blue phases, consisting of different morphologies of long, space-filling double twisted cylinders. Those of cubic spatial symmetry have attracted considerable attention in recent years as templates for soft photonic materials. The latter often requires the creation of monodomains of predefined orientation and size, but their engineering is complicated by a lack of comprehensive understanding of how blue phases nucleate and transform into each other at a submicrometer length scale. In this work, we accomplish this by intercepting nucleation processes at intermediate stages with fast cross-linking of a stabilizing polymer matrix. We reveal using transmission electron microscopy, synchrotron small-angle X-ray diffraction, and angle-resolved microspectroscopy that the grid of double-twisted cylinders undergoes highly coordinated, diffusionless transformations. In light of our findings, the implementation of several applications is discussed, such as temperature-switchable QR codes, micro-area lasing, and fabrication of blue phase liquid crystals with large domain sizes.


1960 ◽  
Vol 38 (1) ◽  
pp. 125-130 ◽  
Author(s):  
James B. Hyne

The results of an n.m.r. study of the diastereoisomeric ephedrine and ψ-ephedrine molecules in non-polar solvents are interpreted and discussed in terms of the relative stabilities of the intramolecularly hydrogen-bonded conformers.


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