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Configuration stability

The difference in concerted reactions is large (5.5 kcal/mole) and no additional factor is needed to explain the high selectivity of the reaction. However, charge-transfer from olefin to aromatic should theoretically be an important stabilizing configuration in this reaction, and one should see if inclusion of CT will modify the conclusion. The charges on the atoms are shown in 17 after transfer of one electron. A contribution of a CT configuration would help to stabilize the preferred orientation relative... [Pg.171]

Available experimental studies of premixed flame stabilization focus on the effect of the bluff-body (stabilizer) configuration, combustion chamber geometry... [Pg.184]

Relatively more stable configurations have even values of L-quantum number (S = 0 and 1 = 6 terms) while relatively unstable configurations correspond to odd values of the L-quantum number (F = 3 and H = 5 terms). It should be noticed that relatively stabilized configurations display a relatively smaller ability to complex formation (less negative values of AG°) and vice versa. In Fig. 1 it is shown that the sequence of L-values has the same double symmetry as the double-double effect. However, no linear correlation has been experimentally observed between changes in the free energy of complex formation or lattice parameters of f-element compounds and the values of the L-quantum number of appropriate f-ions. The lack of such linear correlation is explained in Sect. 5. [Pg.31]

The difference between the observed moment 5.80 and the theoretical value 5.92 we attribute to heme-heme interaction operating to stabilize configurations in which the heme moments are opposed. Why the interaction should decrease the effective moment of ferrihemoglobin, increase that of ferrohemoglobin, and leave that of ferrihemoglobin fluoride unchanged we do not know. [Pg.44]

Figure 90. Surface-stabilized configuration with less than optimum efficiency, switchable between two symmetric states with low optical contrast. The surface pretilt angle has been chosen equal to the smectic tilt angle 0in this example. For a strong boundary condition with zero pretilt, a different extreme limiting condition with approaching zero at the boundary is also conceivable, without any essential difference in the performance of the cell. Figure 90. Surface-stabilized configuration with less than optimum efficiency, switchable between two symmetric states with low optical contrast. The surface pretilt angle has been chosen equal to the smectic tilt angle 0in this example. For a strong boundary condition with zero pretilt, a different extreme limiting condition with approaching zero at the boundary is also conceivable, without any essential difference in the performance of the cell.
If we take a nonzero pretilt into consideration, leading to C1 and C2 structures, thin and thick walls look as illustrated in Fig. 106. In the lower part of that figure we have also illustrated the quite important difference in the polarization and director fields across a Cl and across a C2 structure. It is hard to draw these figures to scale and yet demonstrate the characteristic features. In Fig. 106 the situation may roughly correspond to 0 = 30°, 5 20°, and 10°, such that a + S==9. We may note that the C2 structure is none other than the chevroned version of the surface-stabilized configuration already discussed for Fig. 90. The same C2 configuration n-P would be found for any case with a+5= 6, for instance, with a=3°, S= 15°, and 6= 18°, as long as S<0. [Pg.1664]

An even coarser description is attempted in Ginzburg-Landau-type models. These continuum models describe the system configuration in temis of one or several, continuous order parameter fields. These fields are thought to describe the spatial variation of the composition. Similar to spin models, the amphiphilic properties are incorporated into the Flamiltonian by construction. The Flamiltonians are motivated by fiindamental synnnetry and stability criteria and offer a unified view on the general features of self-assembly. The universal, generic behaviour—tlie possible morphologies and effects of fluctuations, for instance—rather than the description of a specific material is the subject of these models. [Pg.2380]

Hawkins J M, Nambu M and Meyer A 1994 Resolution and configurational stability of the chiral fullerenes C-g, C g, and Cg. A limit for the activation energy of the Stone-Wales transformation J. Am. Chem. Soc. 116 7642-5... [Pg.2425]

For so-called steric stabilization to be effective, tire polymer needs to be attached to tire particles at a sufficiently high surface coverage and a good solvent for tire polymer needs to be used. Under such conditions, a fairly dense polymer bmsh witli tliickness L will be present around the particles. Wlren two particles approach, such tliat r < d + 2L, tire polymer layers may be compressed from tlieir equilibrium configuration, tluis causing a repulsive interaction. [Pg.2679]

In addition to the configuration, electronic stmcture and thennal stability of point defects, it is essential to know how they diffuse. A variety of mechanisms have been identified. The simplest one involves the diffusion of an impurity tlirough the interstitial sites. For example, copper in Si diffuses by hopping from one tetrahedral interstitial site to the next via a saddle point at the hexagonal interstitial site. [Pg.2888]

In the older form of the periodic table, chromium was placed in Group VI, and there are some similarities to the chemistry of this group (Chapter 10). The outer electron configuration, 3d 4s. indicates the stability of the half-filled d level. 3d 4s being more stable than the expected 3d 4s for the free atom. Like vanadium and titanium, chromium can lose all its outer electrons, giving chromium)VI) however, the latter is strongly oxidising and is... [Pg.376]

The electron configuration is the orbital description of the locations of the electrons in an unexcited atom. Using principles of physics, chemists can predict how atoms will react based upon the electron configuration. They can predict properties such as stability, boiling point, and conductivity. Typically, only the outermost electron shells matter in chemistry, so we truncate the inner electron shell notation by replacing the long-hand orbital description with the symbol for a noble gas in brackets. This method of notation vastly simplifies the description for large molecules. [Pg.220]


See other pages where Configuration stability is mentioned: [Pg.138]    [Pg.227]    [Pg.142]    [Pg.309]    [Pg.135]    [Pg.135]    [Pg.309]    [Pg.124]    [Pg.618]    [Pg.824]    [Pg.322]    [Pg.215]    [Pg.70]    [Pg.163]    [Pg.165]    [Pg.165]    [Pg.132]    [Pg.138]    [Pg.227]    [Pg.142]    [Pg.309]    [Pg.135]    [Pg.135]    [Pg.309]    [Pg.124]    [Pg.618]    [Pg.824]    [Pg.322]    [Pg.215]    [Pg.70]    [Pg.163]    [Pg.165]    [Pg.165]    [Pg.132]    [Pg.290]    [Pg.398]    [Pg.403]    [Pg.1693]    [Pg.2424]    [Pg.2537]    [Pg.2564]    [Pg.2888]    [Pg.2938]    [Pg.98]    [Pg.304]    [Pg.17]    [Pg.28]    [Pg.139]    [Pg.389]    [Pg.329]    [Pg.563]    [Pg.453]    [Pg.453]    [Pg.1292]   


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Allyl anions configurational stability

Allyl cations configurational stability

Allyl radicals configurational stability

Benzyllithiums configurational stability

Carbanions configurational stability

Channels configuration, mechanical stability

Chiral configurational stability

Chiral metal complexes configurational stability

Chromium complexes configurational stability

Configurational Stability Racemization and Enantiomerization

Configurational Stability of Carbanions

Configurational entropy, stability

Configurational entropy, stability dispersions

Configurational stability

Configurational stability Grignard reagents

Configurational stability enolates

Configurational stability hemiacetal

Configurational stability lithium carbenoids

Configurational stability organolithium compounds

Configurational stability organozinc compounds

Configurational stability stabilized

Configurational stability unstabilized

Configurational stability, at arsenic

Configurational stability, of organolithium

Crotyl organometallic compounds configurational stability

Cyclopropyl anions configurational stability

Enolate anions configurational stability

NMR investigations on oxaziridines and diaziridines-, configurational stability at nitrogen

Organolithium configurational stability

Oxaziridines configurational stability

Oximes configurational stability

Racemization and Configurational Stability

Silyl anions configurational stability

Stannanes configurational stability

Tertiary arsines configurational stability

Vinyl anions, configurational stability

Vinyllithiums configurational stability

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