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Crystallization combinations

Liquid crystals form a state of matter intermediate between the ordered solid and the disordered liquid. These intermediate phases are called mesophases. In the crystalline state the constituent molecules or ions are ordered in position and orientation, whereas in the liquid state the molecules possess no positional and orientational ordering. Liquid crystals combine to some extent the properties of both the crystalline state (optical and electrical anisotropy) and the liquid state (fluidity). [Pg.140]

A similar phenomenon Is seen In Figure 9, which was In the 90% p-xylene. The top first became flat, and grew Increasing In width. And this part grew to form an Independent crystal In the last picture. However, In this case, the both crystals combined after a short time. [Pg.224]

The structure of most particulate fillers may be classified in terms of their crystalline order and the extent to which these crystals combine together [83]. Three different species may co-exist in a powder ... [Pg.180]

Rod-Like Liquid Crystals Combining RH- and RF-Chains Monolayer Smectic Phases... [Pg.40]

On appreciating such difficulties, recent studies (Parkinson et al., 1974) on homomolecular organic crystals combine the more conventional TSC experiments and trap population by irradiation followed by thermal detrapping... [Pg.181]

The selectivity of liquid crystals, combined with the high efficiency of capillary columns, makes possible the separation of multicomponent mixtures, including critical pairs of isomers. This is illustrated by the separation of alkylbenzenes up to Cc (Figure 4), alkylbenze-to C 6). [Pg.254]

Considering cation-anion interactions, the present structural data can, broadly speaking, be divided into two classes of compounds those that contain a potential of excessive hydrogen bond-making species such as H, HCl, and water of crystallization and those having less or no water of crystallization combined with alkali metal or other size-... [Pg.247]

The deprotonation of (E)-2-butenyl A/,A/-diisopropyl-carbamate leads to (lS,2E)-l-(A(ALdiisopropylcarbamoyloxy)-2-butenyllithium-(—)-sparteine with >90% de after crystallization, combined with a second-order asymmetric transformation (eq 3). It has been applied in the enantioselective synthesis of y-lactones, such as (+)-eldanolide (eq 3), dihydroavermectin Bib, and doubly branched sugar analogs. ... [Pg.502]

From the NMR tracer desorption and self-diffusion data (second and third lines of Table I), one obtains the relation Timm > TmlL. In the example given, intercrystalline molecular exchange is limited, therefore, by transport resistances at the surface of the individual crystals. Combined NMR and high-resolution electron microscopy studies 54) suggest that such surface barriers are caused by a layer of reduced permeability rather than by a mere deposit of impenetrable material on the crystal surface, although that must not be the case in general. [Pg.359]

The Bespak Piezo Electric Actuator is a novel aerosol delivery system based on a piezoelectric crystal combined with an electroformed mesh (Fig. 3). It produces droplets of adjustable size from a single metered drop or fluid reservoir. The mesh hole dimension (as small as 3 pm) determines the size of the droplets produced, whereas the size and density of the holes control the rate of fluid delivery. These can be varied according to the formulation. Although solutions are more readily nebulized, suspensions can be aerosolized if the particle size of the suspended particles is two to three times smaller than the mesh size. [Pg.3856]

Is washed with two 50-mL volumes of half-saturated sodium bicarbonate solution and a mixed solution of saturated sodium bicarbonate (10 mL) and half-saturated sodium chloride (40 ml). The organic layer Is dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue Is subjected to flash column chromatography on silica gel (250 g). Elution with a mixture of ethyl acetate-dlchloromethane-petroleum ether (1 25 25) returns 3.56 g (41t) of unreacted l-(benzenesulfonyl)cyclopentene. Subsequent increase In the solvent polarity to 3 25 25 provides the cycloadduct as a yellowish solid. This material Is dissolved in the minimum amount of dichloromethane to which Is added 25 mL of ether 4.33 g of colorless crystals precipitate. Concentration of the filtrate and crystallization from ether-petroleum ether afford an additional 0.77-1.34 g of light yellow crystals (combined yield of 44-49%) (Note 3). [Pg.164]

The crystal lattice, however, plays a second role. It not only amplifies the diffraction signal from individual molecules, it also serves as half a lens. The X rays scattered by the atoms in a crystal combine together, by virtue of the periodic distribution of their atomic sources, so that their final form is precisely the Fourier transform, that is, the diffraction pattern that we would ordinarily observe at / if we did in fact have an X-ray lens. Thus the situation is not intractable, only difficult. We find in X-ray crystallography that while we cannot record the image plane, we can record what appears at the diffraction plane. It is then up to us to figure out what is on the image plane from what we see on the diffraction plane. [Pg.10]

This result supports the view that diverse ways exist to obtain chiral biomolecules via CPL or chiral inorganic or organic crystals combined with asymmetric autoctalysis. Kenso Soai and his team studied the effect of the structure of the substituents at position 2 of the pyrimidyl alkanol (Shibata et al. 1996). They found that using 2-alkynyl-pyrimidyl alkanol after three rounds of asymmetric autocatalysis, an astonishing amplification factor of 630,0000 was reached. In the reaction, either (+) or (—) crystals of Cytosine serve as initiators that were formed spontaneously by stirring. In the Soai reaction of chiral amplification, it is crucial that dimers of the O-Zinc diisopropyl intermediate are the active catalysts Racemic pyrimidine alcohols subjected to photolysis with either right- or left-handed CPL produced an ee of one isomer as shown in Fig. 3.4. [Pg.28]

Attempts to adapt MALDI-TOF to allow high-throughput analysis [48] have been made, but drawbacks still exist regarding pending sample preparation, matrix effects and the intrinsic inhomogeneity of the sample/matrix crystals combined with the positional resolution of the laser beam. Nevertheless, e.g. for oligonucleotides, it has been shown that autosampler arrays can provide rapid and reproducible results [49]. [Pg.507]

Liquid crystals combine properties of both liquids (fluidity) and crystals (long range order in one, two, or three dimensions). Examples of liquid crystalline templates formed by amphiphiles are lyotropic mesophases, block copolymer mesophases, and polyelectrolyte-suxfactant complexes. Their morphological complexity enables the template synthesis of particles as well as of bulk materials with isotropic or anisotropic morphologies, depending on whether the polymerization is performed in a continuous or a discontinuous phase. As the templating of thermotropic liquid crystals is already described in other reviews [47] the focus here is the template synthesis of organic materials in lyotropic mesophases. [Pg.213]

The low emittance source and bent single crystal combination... [Pg.151]

Four-sided pointed prisms from chloroform, djj 1-5. mp 132. Sublimes at 100. Turns brown and conflagrates at 212 (after melting at 132 ). Tbe dry crystals [combined... [Pg.483]


See other pages where Crystallization combinations is mentioned: [Pg.256]    [Pg.159]    [Pg.91]    [Pg.28]    [Pg.148]    [Pg.174]    [Pg.200]    [Pg.571]    [Pg.53]    [Pg.451]    [Pg.1103]    [Pg.341]    [Pg.123]    [Pg.65]    [Pg.23]    [Pg.67]    [Pg.4]    [Pg.32]    [Pg.79]    [Pg.20]    [Pg.40]    [Pg.159]    [Pg.406]    [Pg.359]    [Pg.291]    [Pg.48]    [Pg.280]    [Pg.526]    [Pg.73]    [Pg.223]    [Pg.276]    [Pg.10]    [Pg.198]   
See also in sourсe #XX -- [ Pg.276 ]




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