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Negative dielectric

If the molecular dipole moment is oriented perpendicularly to the long molecular axis, a material with negative Ae is obtained [31b]. For steric reasons simple lateral monofluorination of an aromatic moiety within the mesogenic core structure does not result in a perpendicular orientation of the molecular dipole moment. This can be achieved only by pair-wise lateral difluorination, which results in mutual cancellation of the respective longitudinal components of the dipole moment vector leaving only the perpendicular contribution. Examples of the most commonly used dielectrically negative materials based on this concept are listed in Table 4.10. [Pg.227]

Table 4.10 Examples for the most commonly used dielectrically negative liquid crystals deriving their dipole moment from lateral difluorination. The virtual clearing points TNi.vin are extrapolated from the Merck mixture ZLI-4792, Af from ZLI-2857 [41]. Table 4.10 Examples for the most commonly used dielectrically negative liquid crystals deriving their dipole moment from lateral difluorination. The virtual clearing points TNi.vin are extrapolated from the Merck mixture ZLI-4792, Af from ZLI-2857 [41].
Dielectrically Negative with Polar Group CH3-0 -Q CH N -O OCO - C3H7- n... [Pg.158]

A common feature of a binary mixed system of N +Np is that the melting point rises steeply as either of the two components increases. An example for an Nn+Np binary system is given in Fig. 9. A mixed binary system of cyclohexanecarboxylate (ECH) as the dielectrically negative type LC and biphenyl as the dielectrically positive type LC gives a poor alloying system. A poor alloying tendency is also seen in a binary system in which the components Nn and Np have similar chemical structure. [Pg.161]

As we have already stated, we know by experience that LCs consisting of dielectrically positive (Np) type molecules have poor AV values, while those consisting of mixtures of dielectrically negative (Nn) and dielectrically positive material (Np) give good AV° values as shown in Fig. 8. [Pg.167]

Solvent Effects on the Rate of Substitution by the S l Mechanism Table 8 6 lists the relative rate of solvolysis of tert butyl chloride m several media m order of increasing dielectric constant (e) Dielectric constant is a measure of the ability of a material m this case the solvent to moderate the force of attraction between oppositely charged par tides compared with that of a standard The standard dielectric is a vacuum which is assigned a value e of exactly 1 The higher the dielectric constant e the better the medium is able to support separated positively and negatively charged species 8olvents... [Pg.345]

The ultimate trapping site for a photoelectron is influenced by the high dielectric constant of silver haUde (ca 12.5, 11.15, and 7.15 for AgBr, AgCl, and P-AgI, respectively), the negative surface charge, and relative trap depths. Interior traps located at point defects on dislocation lines are probably not as... [Pg.446]

The dielectric constant is a measure of the ease with which charged species in a material can be displaced to form dipoles. There are four primary mechanisms of polarization in glasses (13) electronic, atomic, orientational, and interfacial polarization. Electronic polarization arises from the displacement of electron clouds and is important at optical (ultraviolet) frequencies. At optical frequencies, the dielectric constant of a glass is related to the refractive index k =. Atomic polarization occurs at infrared frequencies and involves the displacement of positive and negative ions. [Pg.333]

This gas is electronegative and its molecules quickly absorb the free electrons in the arc path between the contacts to form negatively charged ions. This apparent trapping of the electrons results in a rapid build-up of dielectric strength after a current zero. The detailed. sequence of arc extinction may be summarized as follows. [Pg.638]

The mechanism of the cycloaddition of phenyl azide to norbornene has been shown to involve a concerted mechanism with a charge imbalance in the transition state (199). In a similar manner the cycloaddition of phenyl azide to enamines apparently proceeds by a concerted mechanism (194, 194a). This is shown by a rather large negative entropy of activation (—36 entropy units for l-(N-morpholino)cyclopentene in benzene solvent at 25°C), indicative of a highly ordered transition state. Varying solvents from those of small dielectric constants to those of large dielectric constants has... [Pg.244]

A ferroelectric crystal is one that has an electric dipole moment even in the absence of an external electric held. This arises because the centre of positive charge in the crystal does not coincide with the centre of negative charge. The phenomenon was discovered in 1920 by J. Valasek in Rochelle salt, which is the H-bonded hydrated d-tartrate NaKC4H406.4H 0. In such compounds the dielectric constant can rise to enormous values of lO or more due to presence of a stable permanent electric polarization. Before considering the effect further, it will be helpful to recall various dehnitions and SI units ... [Pg.57]

If we apply an external electrostatic field E then the protons and electrons each experience a force. This force tends to cause charge separation in the dielectric. The positively charged nuclei move in the direction of the applied field, the negatively charged electrons move in the opposite direction. I have illustrated this behaviour in Figure 15.3. [Pg.256]


See other pages where Negative dielectric is mentioned: [Pg.118]    [Pg.288]    [Pg.158]    [Pg.161]    [Pg.163]    [Pg.164]    [Pg.126]    [Pg.127]    [Pg.118]    [Pg.288]    [Pg.158]    [Pg.161]    [Pg.163]    [Pg.164]    [Pg.126]    [Pg.127]    [Pg.219]    [Pg.440]    [Pg.841]    [Pg.1696]    [Pg.623]    [Pg.93]    [Pg.346]    [Pg.400]    [Pg.199]    [Pg.414]    [Pg.447]    [Pg.52]    [Pg.207]    [Pg.509]    [Pg.128]    [Pg.1613]    [Pg.2011]    [Pg.559]    [Pg.631]    [Pg.631]    [Pg.164]    [Pg.1222]    [Pg.1230]    [Pg.84]    [Pg.101]    [Pg.337]    [Pg.346]    [Pg.35]    [Pg.38]    [Pg.299]   
See also in sourсe #XX -- [ Pg.2 , Pg.243 ]

See also in sourсe #XX -- [ Pg.2 , Pg.243 ]




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