-
6
-
-
0003872521
-
-
D. Demus, J. Goodby, G. W. Gray, H. W. Spiess and V. Vill, Weinheim, Wiley-VCH, p. 969
-
T. Kato, in Handbook of Liquid Crystals, ed., D. Demus, J. Goodby, G. W. Gray, H. W. Spiess and V. Vill, Weinheim, Wiley-VCH, p. 969
-
Handbook of Liquid Crystals, ed.
-
-
Kato, T.1
-
13
-
-
33644771568
-
Anisotropic Organic Materials - Approaches to Polar Order
-
p. 281
-
D. M. Walba, E. Körblova, R. Shao, J. E. Maclennan, D. E. Link, M. A. Glaser and N. A. Clark, Anisotropic Organic Materials - Approaches to Polar Order, ACS Symp. Ser., vol. 789, p. 281
-
ACS Symp. Ser.
, vol.789
-
-
Walba, D.M.1
Körblova, E.2
Shao, R.3
Maclennan, J.E.4
Link, D.E.5
Glaser, M.A.6
Clark, N.A.7
-
20
-
-
33845506370
-
-
A. Ciferri., CRC Press, Taylor and Francis group, Boca Raton
-
Supramolecular Polymers, ed., A. Ciferri., CRC Press, Taylor and Francis group, Boca Raton
-
Supramolecular Polymers, ed.
-
-
-
21
-
-
33644766295
-
-
The synthesis of the desired bent-complexes required the H donor and H acceptor to be mixed in precise equimolecular proportions in a common solvent (THF), followed by slow removal of the solvent. The formation and thermal stability of the complex was confirmed by IR spectroscopy (see ESI) and through OM measurements: the solid samples melted cleanly without the appearance of biphasic regions
-
The synthesis of the desired bent-complexes required the H donor and H acceptor to be mixed in precise equimolecular proportions in a common solvent (THF), followed by slow removal of the solvent. The formation and thermal stability of the complex was confirmed by IR spectroscopy (see ESI) and through OM measurements: the solid samples melted cleanly without the appearance of biphasic regions
-
-
-
-
22
-
-
33644766296
-
-
In some cases, virgin semicrystalline samples of these polymers did not form mesophase on heating but all of them were mesomorphic on successive thermal treatments after they had first been melted to the isotopic liquid
-
In some cases, virgin semicrystalline samples of these polymers did not form mesophase on heating but all of them were mesomorphic on successive thermal treatments after they had first been melted to the isotopic liquid
-
-
-
-
23
-
-
33644778027
-
-
The high viscosity of these polymers prevented cell filling by capillary action and so their electrooptic characterization was not possible
-
The high viscosity of these polymers prevented cell filling by capillary action and so their electrooptic characterization was not possible
-
-
-
-
25
-
-
33644774969
-
-
To avoid premature thermal polymerization of the reactive complexes 200 ppm of a thermal inhibitor (2,6-di-tert-butyl-4-methylphenol) was added to the samples, but partial thermal polymerization of the complexes 1-M6, 2-M6 and 2-M11 was observed on heating, limiting any comparative study
-
To avoid premature thermal polymerization of the reactive complexes 200 ppm of a thermal inhibitor (2,6-di-tert-butyl-4-methylphenol) was added to the samples, but partial thermal polymerization of the complexes 1-M6, 2-M6 and 2-M11 was observed on heating, limiting any comparative study
-
-
-
-
26
-
-
33644754261
-
-
The photopolymerization of 1-M11 was carried out using a photo-DSC experimental setup equipped with a 365 nm lamp and samples containing 1% (w/w) of Irgacure 369 and 200 ppm of the thermal inhibitor 2,6-di-tert-butyl-4- methylphenol. The liquid crystalline properties of the monomer were not noticeably modified for the blends
-
The photopolymerization of 1-M11 was carried out using a photo-DSC experimental setup equipped with a 365 nm lamp and samples containing 1% (w/w) of Irgacure 369 and 200 ppm of the thermal inhibitor 2,6-di-tert-butyl-4- methylphenol. The liquid crystalline properties of the monomer were not noticeably modified for the blends
-
-
-
-
28
-
-
33644745596
-
-
Samples of 1-M11 were subjected to electric fields to ensure a ferroelectric SmCP order before polymerization. However, despite the proven switching of the monomer, as soon as a DC voltage was applied, the sample polymerized to give opaque films without SHG activity under a 1064 nm laser
-
Samples of 1-M11 were subjected to electric fields to ensure a ferroelectric SmCP order before polymerization. However, despite the proven switching of the monomer, as soon as a DC voltage was applied, the sample polymerized to give opaque films without SHG activity under a 1064 nm laser
-
-
-
|