Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Polar-nonpolar interactions

Another example of a system with (polar + nonpolar) interactions is shown in Figure 17.7, where curve 1 shows for mixing non-polar tetrachloro-methane molecules with polar acetonitrile molecules.10 The breaking of (dipole + dipole) interactions in the acetonitrile when mixed with tetrachloro-methane results in a large positive H... [Pg.283]

The inter-molecular interactions in the polymers include the overlapping repulsion between atoms, the ion-ion interactions, ion-induced-dipole interactions, dipole-dipole interactions, polar-nonpolar interactions, and nonpolar-nonpolar interactions, etc. For the van der Waals interactions between the nonpolar polymers, about 70 % of the attractive interactions are sourced from the dispersion forces, which are instant dipole-dipole interactions induced by the vibration of the substituted groups in the chains. The frequency of vibration influences the refractivity, so the forces are named with dispersion forces. The dispersion forces within a pair of neighboring groups can be expressed as... [Pg.46]

Surface tension, 7, is a key parameter in describing a surface. It is defined as the reversible work associated with the creation of truncated bonds and molecular conformations that occur at the surface (outside of the bulk). For any given material, the Uterature typically offers a range of values for y, which is a testament to the experimental and theoretical complexities of its determination. Table 9 hsts one compilation of the surface energies of common polymers, both the composite value and the breakdown by polar/nonpolar interactions. Fluorocarbons and polyolefins are quite low in polar functionality and thus have... [Pg.26]

When viscometric measurements of ECH homopolymer fractions were obtained in benzene, the nonperturbed dimensions and the steric hindrance parameter were calculated (24). Erom experimental data collected on polymer solubiUty in 39 solvents and intrinsic viscosity measurements in 19 solvents, Hansen (30) model parameters, 5 and 5 could be deterrnined (24). The notation 5 symbolizes the dispersion forces or nonpolar interactions 5 a representation of the sum of 8 (polar interactions) and 8 (hydrogen bonding interactions). The homopolymer is soluble in solvents that have solubility parameters 6 > 7.9, 6 > 5.5, and 0.2 < <5.0 (31). SolubiUty was also determined using a method (32) in which 8 represents the solubiUty parameter... [Pg.555]

Closely related to the London interaction is the dipole-induced-dipole interaction, in which a polar molecule interacts with a nonpolar molecule (for example, when oxygen dissolves in water). Like the London interaction, the dipole—induced-dipole interaction arises from the ability of one molecule to induce a dipole moment in the other. However, in this case, the molecule that induces the dipole moment has a permanent dipole moment. The potential energy of the interaction is... [Pg.305]

Regardless of the relative importance of polar and nonpolar interactions in stabilizing the cyclohexaamylose-DFP inclusion complex, the results derived for this system cannot, with any confidence, be extrapolated to the chiral analogs. DFP is peculiar in the sense that the dissociation constant of the cyclohexaamylose-DFP complex exceeds the dissociation constants of related cyclohexaamylose-substrate inclusion complexes by an order of magnitude. This is probably a direct result of the unfavorable entropy change associated with the formation of the DFP complex. Thus, worthwhile speculation about the attractive forces that lead to enantiomeric specificity must await the measurement of thermodynamic parameters for the chiral substrates. [Pg.239]

The Separated Associated Fluid Interaction Model for Polar + Nonpolar Mixtures... [Pg.441]

In addition to the choice of Lewis acid, added common ion salt, and temperature, the fast equilibrium between active and dormant species can be fostered by including additional nucleophiles (separate from the nucleophilic counterion) in the reaction system and by variations in solvent polarity. Nucleophiles act by further driving of the dynamic equilibrium toward the covalent species and/or decreasing the reactivity of ion pairs. Nucleophilic counterions and added nucleophiles work best in nonpolar solvents such as toluene and hexane. Their action in polar solvents is weaker because the polar solvents interact with the nucleophiles and nucleophilic counterions, as well as the ion pairs. Polar solvents such as methylene... [Pg.404]

Testosterone metabolism. The lipido-ste-rol extract (LSESr, Permixon) was studied in primary cultures of epithelial cells and fibroblasts separated from benign prostate hypertrophy and prostate cancer tissues. The extract inhibited the formation of the T metabolites androstenedione 5 4 and 5 a-DHT The lipophilic extracts of fruits inhibited T 5p-reductase (EC 1.3.99.5) (5(xR). For fatty acid-like 5(xR inhibition a strongly polar end-group and a molecular skeleton allowing nonpolar interactions with the enzyme were required. The result indicated that 5pR activity in prostatic tissue may be influenced by the lipid environ-... [Pg.477]

Nonpolar (hydrophobic) compounds dissolve poorly in water they cannot hydrogen-bond with the solvent, and their presence forces an energetically unfavorable ordering of water molecules at their hydrophobic surfaces. To minimize the surface exposed to water, nonpolar compounds such as lipids form aggregates (micelles) in which the hydrophobic moieties are sequestered in the interior, associating through hydrophobic interactions, and only the more polar moieties interact with water. [Pg.58]

For the case of a polar molecule interacting with a nonpolar molecule, an induction energy term should be considered see Section 13.5 of [178]. This additional interaction modifies the interaction parameters as... [Pg.500]

Polar + Nonpolar Mixtures Figure 17.6 summarizes HC m, and for mixtures of 1-chlorobutane with heptane.9 We note that for this system is significantly larger than for any of the (nonpolar + nonpolar) systems described previously. A major contribution to H is the energy required to break apart the (dipole + dipole) interaction between the polar 1-chlorobutane molecules. Thus, if A-A represents (heptane + heptane) interactions and B-B represents (1-chlorobutane + 1-chlorobutane) interactions, with A-B representing (1-chlorobutane-I-heptane) interactions, then energy is required to break apart A-A that is not recovered when A-B forms, and H is positive. [Pg.283]


See other pages where Polar-nonpolar interactions is mentioned: [Pg.66]    [Pg.189]    [Pg.133]    [Pg.293]    [Pg.487]    [Pg.713]    [Pg.1668]    [Pg.282]    [Pg.66]    [Pg.189]    [Pg.133]    [Pg.293]    [Pg.487]    [Pg.713]    [Pg.1668]    [Pg.282]    [Pg.394]    [Pg.490]    [Pg.198]    [Pg.28]    [Pg.445]    [Pg.80]    [Pg.194]    [Pg.579]    [Pg.185]    [Pg.27]    [Pg.98]    [Pg.91]    [Pg.356]    [Pg.464]    [Pg.364]    [Pg.334]    [Pg.317]    [Pg.624]    [Pg.212]    [Pg.467]    [Pg.378]    [Pg.31]    [Pg.637]    [Pg.301]    [Pg.198]    [Pg.583]    [Pg.750]    [Pg.849]    [Pg.844]   
See also in sourсe #XX -- [ Pg.36 ]




SEARCH



Nonpolar

Nonpolar interactions

Nonpolar polar

Nonpolarized

Polar and Nonpolar Interactions Encoded in Lipophilicity

Polar interactions

Polarization interaction

© 2024 chempedia.info