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Dipole steric

Recognition and description of new interparticle interaction forces such as those owing to magnetic dipoles, steric and electrosteric repulsion,... [Pg.178]

Buckingham and Pople gave a more complete treatment than Stockmayer s of the interaction between two molecules having non-central force fields. Their treatment allows not only for dipole-dipole interaction but also for dipole-quadrupole, quadrupole-quadrupole, dipole-induced dipole, steric, anisotropic, and other effects. An important feature of the Buckingham-Pople procedure is that the various integrals needed can be calculated from a master table that they give. Buckingham and Pople applied their method to four polar compounds for which values of the dipole moment and the polarizability were known, and used B(T) to... [Pg.198]

As we have repeatedly stressed, flexoelec-tricity is a phenomenon that is a priori independent of chirality. But we have also seen that some flexoelectric deformations do have a tendency to occur spontaneously in a chiral medium. All except the helical C state are, however, suppressed, because they are not space-filling. A flexoelectric deformation may of course also occur spontaneously in the nonchiral case, namely, under exactly the same conditions where the deformation is space-filling and does not give rise to defect structures. In other words, in creating the twist-bend structure which is characteristic of a helielectric. Imagine, for instance, that we have mesogens which have a pronounced bow shape and, in addition, some lateral dipole. Sterically they would prefer a helicoidal structure, as depicted in Fig. 52, which would minimize the elastic... [Pg.1595]

Absorption, metaboHsm, and biological activities of organic compounds are influenced by molecular interactions with asymmetric biomolecules. These interactions, which involve hydrophobic, electrostatic, inductive, dipole—dipole, hydrogen bonding, van der Waals forces, steric hindrance, and inclusion complex formation give rise to enantioselective differentiation (1,2). Within a series of similar stmctures, substantial differences in biological effects, molecular mechanism of action, distribution, or metaboHc events may be observed. Eor example, (R)-carvone [6485-40-1] (1) has the odor of spearrnint whereas (5)-carvone [2244-16-8] (2) has the odor of caraway (3,4). [Pg.237]

V n der W ls Interactions. Van der Waals iateractions result from the asymmetric distribution of electronic charge surrounding an atom, which induces a complementary dipole in a neighboring atom, resulting in an attractive force. In general, the attractive force of van der Waals interactions is very weak (<4.2 kJ/mol (1 kcal/mol)) but may become significant if steric complementarity creates an opportunity to form a large number of van der Waals attractions. [Pg.196]

There is Httie known chemistry of tetrakis-Cp thorium complexes. Pseudotetrahedral molecules, (rj-ring) Tb (15), where ring = Cp [1298-75-5] or Ind [11133-17-6], have a measurable dipole, resulting from deviation of symmetry (88). Difference of coordination environments, eg, v] in the indenyl system and in the Cp system, appears to indicate great steric crowding about the thorium center, which probably limits the reactivity and synthetic derivatization of these complexes. [Pg.42]

A study of the effect of substitution patterns in oxadiazoles and isoxazoles and their effect on the UV spectra in the lO -lO M concentration range was performed. Hypso-chromic effects and deviations from Beer s law were observed and were believed to be associated with antiparallel, sandwich-type self-association via dipole-dipole interactions. Beer s law is followed when the molecular dipole moments are small or when self-association is sterically hindered. [Pg.4]

Figure 4.2. Rotational-energy barriers as a function of substitution. Tbe small barrier ( 2kcal) in ethane (a) is lowered even further ( O.Skcal) if three bonds are tied back by replacing three hydrogen atoms of a methyl group by a triple-bonded carbon, as in methylacetylene (b). The barrier is raised 4.2 kcal) when methyl groups replace the smaller hydrogen atoms, as in neopentane (c). Dipole forces raise the barrier further ( 15 kcal) in methylsuccinic acid (d) (cf. Figure 4.3). Steric hindrance is responsible for the high barrier (> 15 kcal) in the diphenyl derivative (e). (After... Figure 4.2. Rotational-energy barriers as a function of substitution. Tbe small barrier ( 2kcal) in ethane (a) is lowered even further ( O.Skcal) if three bonds are tied back by replacing three hydrogen atoms of a methyl group by a triple-bonded carbon, as in methylacetylene (b). The barrier is raised 4.2 kcal) when methyl groups replace the smaller hydrogen atoms, as in neopentane (c). Dipole forces raise the barrier further ( 15 kcal) in methylsuccinic acid (d) (cf. Figure 4.3). Steric hindrance is responsible for the high barrier (> 15 kcal) in the diphenyl derivative (e). (After...
There are probably several factors which contribute to determining the endo exo ratio in any specific case. These include steric effects, dipole-dipole interactions, and London dispersion forces. MO interpretations emphasize secondary orbital interactions between the It orbitals on the dienophile substituent(s) and the developing 7t bond between C-2 and C-3 of the diene. There are quite a few exceptions to the Alder rule, and in most cases the preference for the endo isomer is relatively modest. For example, whereas cyclopentadiene reacts with methyl acrylate in decalin solution to give mainly the endo adduct (75%), the ratio is solvent-sensitive and ranges up to 90% endo in methanol. When a methyl substituent is added to the dienophile (methyl methacrylate), the exo product predominates. ... [Pg.638]

When both the 1,3-dipoIe and the dipolarophile are unsymmetrical, there are two possible orientations for addition. Both steric and electronic factors play a role in determining the regioselectivity of the addition. The most generally satisfactory interpretation of the regiochemistry of dipolar cycloadditions is based on frontier orbital concepts. As with the Diels-Alder reaction, the most favorable orientation is that which involves complementary interaction between the frontier orbitals of the 1,3-dipole and the dipolarophile. Although most dipolar cycloadditions are of the type in which the LUMO of the dipolarophile interacts with the HOMO of the 1,3-dipole, there are a significant number of systems in which the relationship is reversed. There are also some in which the two possible HOMO-LUMO interactions are of comparable magnitude. [Pg.647]

The positions of substitution, orientation, and configuration of the stable form are determined by a balance between opposing steric and dipole ef-fects. There is less agreement regarding the factors influencing kinetically controlled reaction (see below). Essentially neutral conditions, such as provided by an acetate or pyridine buffer, are required to avoid isomerization. Frequently, however, bromination will not proceed under these conditions, and a compromise has been used in which a small amount of acid is added to start and maintain reaction, while the accumulation of hydrogen bromide is prevented by adding exactly one equivalent of acetate... [Pg.270]

Compare energies for both diaxial and diequatorial chair conformers of trans-l,2-difluorocyclohexane (X = F). Which conformer is preferred Does the preferred conformer minimize steric repulsion Explain. Examine dipole moments for the two conformers. Does the preferred conformer minimize electrostatic repulsion (or maximize electrostatic attraction) Explain. [Pg.80]

K-K Complexation Hydrogen bonding Inclusion Dipole stacking Steric interactions Anionic or cationic binding... [Pg.28]

The brush-type (Pirkle-type) CSPs have been used predominantly under normal phase conditions in LC. The chiral selector typically incorporates tt-acidic and/or n-basic functionality, and the chiral interactions between the analyte and the CSP include dipole-dipole interactions, n-n interactions, hydrogen bonding, and steric hindrance. The concept of reciprocity has been used to facilitate the rational design of chiral selectors having the desired selectivity [45]. [Pg.307]

In this equation, AG°CS is taken to be negligible for p- and y-cyclodextrin systems and to be constant, if there is any, for the a-cyclodextrin system. The AG W term is virtually independent of the kind of guest molecules, though it is dependent on the size of the cyclodextrin cavity. The AG dw term is divided into two terms, AG°,ec and AGs°ter, which correspond to polar (dipole-dipole or dipole-induced dipole) interactions and London dispersion forces, respectively. The former is mainly governed by the electronic factor, the latter by the steric factor, of a guest molecule. Thus, Eq. 2 is converted to Eq. 3 for the complexation of a particular cyclodextrin with a homogeneous series of guest molecules ... [Pg.67]

The steric and dipole-dipole effects of the CF3 group on valence isomerization in the Dewar pyridine-azaprismane-pyridine system have been studied. These reveal themselves in the high stability, compared to the pyridine, of the valence isomer arising out of the large activation energy for rearomatization. The transformation of a 1-Dewar to 2-Dewar pyridine was observed (89T3115). [Pg.26]

Since the elementary quantum-mechanical treatment does not seem to give a high enough barrier, various treatments of the problem have been proposed which use empirical data such as bond dipole moments and steric repulsive forces. These treatments do not introduce any new forces which would not be included in a proper quantum-mechanical analysis, but they attempt to short-circuit these difficult and uncertain calculations. [Pg.389]

NMR measurements indicate that the equilibrium constant varies with the polarity of the solvent and temperature. The more polar the solvent, the greater the fraction of sulfoxide at equilibrium which is consistent with the greater dipole moment of the sulfoxide as compared with the sulfenate. Increasing temperature results in a reverse effect, due to the steric hindrance in the sulfoxide which becomes more marked at higher temperatures. These results are the first published evidence for the reversibility of the sulfenate-sulfoxide rearrangement and illustrate the occurrence of the rearrangement unsuccessfully attempted by Cope39. [Pg.722]

In addition to the geometric, steric effects which flexibility directly modifles, all intramolecular electronic properties of a flexible molecule are also coupled to molecular structure. In a real material, such properties as molecular dipole. [Pg.29]

Fig. 2a-f. Mesogenic molecules with differing degrees of polar and sterical asymmetry a symmetric molecule with rigid core and two hydrocarbon tails b terminally polar molecule (arrow indicates the permanent dipole) c swallow-tailed (hiforked) molecule d hanana shaped molecule e terminally fluorinated molecule f polyphilic molecule (hatched areas correspond to the fluorinated fragment)... [Pg.205]

Many of the mesogenic molecules are stericaUy asymmetric, which is determined by the fractures and bending of the molecular core as well as by the presence of the tail chains of different nature, including the branched, biforked or polyphilic moieties (Fig. 2c-f). In terms of the multipole model of molecular asymmetry introduced by Petrov and Derzhanski [34], we can speak about longitudinal or transverse steric dipoles or multipoles (Fig. 3). [Pg.206]


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See also in sourсe #XX -- [ Pg.10 , Pg.12 , Pg.15 , Pg.19 , Pg.20 , Pg.24 , Pg.25 , Pg.27 ]




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