Acids liquid crystals

Pentafluoroaniline. Pentafluoroaniline [771 -60-8] i2is been prepared from amination of hexafluoroben2ene with sodium amide inbquid ammonia or with ammonium hydroxide in ethanol (or water) at 167—180°C for 12—18 h. It is weakly basic (p = 0.28) and dissolves only in concentrated acids. Liquid crystals have been prepared from Schiff bases derived from pentafluoroaniline (230). 

Qualitative analysis of chiral compounds, including drugs, pesticides, carbohydrates, amino acids, liquid crystals, and other biochemicals Determination of enantiomeric purity of chiral compounds... 

For background information on infrared spectral changes with changes of phase such as might occur in the lubricant under shear, infrared emission spectra were obtained under static conditions at different temperatures. For this purpose, a small amount of liquid crystal was sandwiched between a KBr window and a stainless steel plate and emission spectra were obtained at different temperatures. The thickness of the layer was not determined but judging from the spectra, must have been about 1.0 pm. Stainless steel had to be used to avoid chemical reaction with acidic liquid crystal. 

Nucleic acid liquid crystals - from phase elucidation to chromatin regulation a) F. Livolant,... 

Polyester sheet products may be produced from amorphous poly(ethylene terephalate) (PET) or partiaHy crystallized PET. Acid-modified (PETA) and glycol modified (PETG) resins are used to make ultraclear sheet for packaging. Poly(butylene terephthalate) (PBT) has also been used in sheet form. Liquid-crystal polyester resins are recent entries into the market for specialty sheet. They exhibit great strength, dimensional stabHity, and inertness at temperatures above 250°C (see Polyesters,thermoplastic). 

Liquid crystal polyesters are made by a different route. Because they are phenoHc esters, they cannot be made by direct ester exchange between a diphenol and a lower dialkyl ester due to unfavorable reactivities. The usual method is the so-called reverse ester exchange or acidolysis reaction (96) where the phenoHc hydroxyl groups are acylated with a lower aHphatic acid anhydride, eg, acetic or propionic anhydride, and the acetate or propionate ester is heated with an aromatic dicarboxyHc acid, sometimes in the presence of a catalyst. The phenoHc polyester forms readily as the volatile lower acid distills from the reaction mixture. Many Hquid crystal polymers are derived formally from hydroxyacids (97,98) and thein acetates readily undergo self-condensation in the melt, stoichiometric balance being automatically obtained. 

NHydroxyben2oic acid is of significant commercial importance. The most familiar application is the use of several of its esters as preservatives, known as parabens. Also of interest is the use in liquid crystal polymer applications. 

The homopolymers of p-hydroxybenzoic acid have such a high value for the that they are somewhat intractable. Useful materials may, however, be made by copolymerising with a view to introducing some molecular flexibility or reducing chain packing or introducing some non-linear links. Commercially important liquid crystal polyesters are discussed in Chapter 25. 

For the liquid crystal polyesters the basic structural units are derived from such materials as 5-hydroxybenzoic acid, terephthalic acid and hydroquinone. Some basic sequences from such materials are shown in Figure 25.25. 

Answer An electronic temperature monitor could be equipped with a bar-code liquid crystal display which could be read by a portable bar-code reader. These devices have a memory so several readings may be taken before they are readout over a telephone modem to a data logging computer. The simplest way to read the acid type would be to post a label that is bar-coded to indicate the acid type. Tire acid quantity could be indicated by an acid level gage using a bar-code display of the level. The aluminum quality could be indicated by displaying a label in bar-code. The amount of aluminum could be determined by weight using a bar-code readout on the scales. 

The ether is allowed to evaporate on the water-bath and th e nitrile is then hydrolysed by continuing to heat it on the water-bath with the addition of 4—5 times its volume of cone, hydrochloiic acid until crystals appear on the surface. Water is added and the hot liquid decanted and filteied from any oil. On cooling, the crystals are filtered, washed vvith a little cold ivaterand dried. A fuither quantity can be extiacted from the filtrate with ether. It may be recrystallised from benzene. Yield, 10—15 grms. 

Plastics can be used to make erasable printing media by a number of different techniques. Photo changing dyes could be incorporated into the structure of the plastics. The printer could change the dye to the colored form to read, and the material can be bleached with another unit that would reverse the photo coloring process. An ionic type plastic can be incorporated into the plastics and used to color the printed area by the use of an indicator type reaction with an organic acid or base. Another method would be to use a thermal printer in conjunction with liquid crystal type materials that would alter the state of the liquid crystals in the printed areas. Applying heat and electrical fields to the printed sheet would erase the printing. 

Alcohols, reaction of isocyanates with, 224-225 Alcoholysis, 69 Alicyclic dianhydrides, 297 Alignment coating, for liquid crystal devices, 269-270 Aliphatic AA-BB-type polyamides, synthesis of, 164-173 Aliphatic AB-type polyamides, 173-180 Aliphatic acids, 60... 

Typically the formulation may contain up to 60% active with builder salts and a water level of about 30-40% [52]. The weight ratio of LAS/AE may range from 1.5 1 up to 4 1. The combination of LAS and AE is especially effective for two reasons. First, LAS and AE interact strongly to form the lamellar phase liquid crystals. Second, both ingredients can be introduced into the liquid formulation as a 95 + % active liquid to control the amount of water going into the formulation. LAS can be introduced into the formulation as sulfonic acid and neutralized in situ. 

FIG. 35 The phase behavior of dodecane sulfonic acid with water. O, Doubly refracting material appears as the isotropic solution is cooled. <3, Isotropic solution appears as the liquid crystal is heated. CD, Crystalline solid disappears on heating. Pairs of solid points connected with the vertical dashed lines mark the appearance and disappearance of pseudoisotropy as samples are heated. The area ABC, within which the intermediate mesophase exists alone, is not precisely determined. 

The raw materials from which di-D-fructose dianhydrides can be obtained in appreciable yield are readily available from comparatively inexpensive agricultural feedstocks. Thus, these compounds are attractive as chiral-starting materials for chemical synthesis. Their stability to acid and heat, and their relative rigidity, because of the conformational constraints covered here, are also features that might be exploited during syntheses.119 A series of variously substituted di-D-fructose dianhydrides has been prepared,119 starting from 6,6 -dideoxy-6,6 -di-halosucroses. The properties of these and other derivatives of di-D-fructose dianhydrides are summarized in Tables XIV-XX. Two of these derivatives, 48 and 56, exhibit thermotropic liquid-crystal properties.119... 

In order to make polymers behave as liquid crystals it is necessary to introduce some structural rigidity. A typical polymer which has the required rigidity is poly(phenylenetetraphthalamide) (10.7). This material belongs to a class of polymer known as the aramids. Other liquid crystalline polymers are the thermotropic polyesters derived from /7-hydroxybenzoic acid, p, p -biphenol and terephthalic acid (10.8). 

To date, the crystal structures of more than 200 mesogenic compounds are known. In this review, we wish to present a general overview of the crystal structures of mesogenic compounds up to the end of 1997. Unfortunately, it is not possible to consider the crystal structure determinations of carbohydrate liquid crystals [13, 14], metallomesogens [15-18], phasmid and biforked mesogens [19-22], perfluorinated mesogenic compounds [23-27], benzoic acids [6, 28-31], cinnamic acids [7, 32, 33], dicarboxylic acids [34, 35], cinnamate compounds [8, 36-40], and discotic liquid crystals [41-43] due to the lack of space. 

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