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High small-molecules

Several VTST techniques exist. Canonical variational theory (CVT), improved canonical variational theory (ICVT), and microcanonical variational theory (pVT) are the most frequently used. The microcanonical theory tends to be the most accurate, and canonical theory the least accurate. All these techniques tend to lose accuracy at higher temperatures. At higher temperatures, excited states, which are more difficult to compute accurately, play an increasingly important role, as do trajectories far from the transition structure. For very small molecules, errors at room temperature are often less than 10%. At high temperatures, computed reaction rates could be in error by an order of magnitude. [Pg.167]

Evaporation Retardants. Small molecule solvents that make up the most effective paint removers also have high vapor pressure and evaporate easily, sometimes before the remover has time to penetrate the finish. Low vapor pressure cosolvents are added to help reduce evaporation. The best approach has been to add a low melting point paraffin wax (mp = 46-57° C) to the paint remover formulation. When evaporation occurs the solvent is chilled and the wax is shocked-out forming a film on the surface of the remover that acts as a barrier to evaporation (5,6). The addition of certain esters enhances the effectiveness of the wax film. It is important not to break the wax film with excessive bmshing or scraping until the remover has penetrated and lifted the finish from the substrate. Likewise, it is important that the remover be used at warm temperatures, since at cool temperatures the wax film may not form, or if it does it will be brittle and fracture. Rapid evaporation occurs when the wax film is absent or broken. [Pg.550]

S of large and small molecules ia several polymers. A low D and a high S mean that lo ss of flavor/aroma molecules into a polymer package wall can be ... [Pg.436]

The apphcation of a high electric field across a thin conjugated polymer film has shown the materials to be electroluminescent (216—218). Until recentiy the development of electroluminescent displays has been confined to the use of inorganic semiconductors and a limited number of small molecule dyes as the emitter materials. Expansion to the broad array of conjugated polymers available gives advantages in control of emission frequency (color) and facihty in device fabrication as a result of the ease of processibiUty of soluble polymers (see Chromogenic materials,electrochromic). [Pg.45]

Sephasorb HP (ultrafine, prepared by hydroxypropylation of crossed-linked dextran) can also be used for the separation of small molecules in organic solvents and water, and in addition it can withstand pressures up to 1400 psi making it useful in HPLC. These gels are best operated at pH values between 2 and 12, because solutions with high and low pH values slowly decompose them (see further in Chapter 6). [Pg.24]

Step 1 of the parametrization process is the selection of the appropriate model compounds. In the case of small molecules, such as compounds of pharmaceutical interest, the model compound may be the desired molecule itself. In other cases it is desirable to select several small model compounds that can then be connected to create the final, desired molecule. Model compounds should be selected for which adequate experimental data exist, as listed in Table 1. Since in almost all cases QM data can be substimted when experimental data are absent (see comments on the use of QM data, above), the model compounds should be of a size that is accessible to QM calculations using a level of theory no lower than HE/6-31G. This ensures that geometries, vibrational spectra, conformational energetics, and model compound-water interaction energies can all be performed at a level of theory such that the data obtained are of high enough quality to accurately replace and... [Pg.23]

B3) These variations are related to the refinement procedures much more than to the experimental data [23] and are generally larger than in high resolution structures of small molecules. In MD calculations with harmonic bond lengths and bond angles they are still higher. [Pg.118]


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