Big Chemical Encyclopedia

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

Articles Figures Tables About

Optical solvent

Pure ionic liquids (ILs) are solvents that remain colorless and transparent throughout almost the whole visible and near-infrared (NIR) spectral regions. This property coupled with excellent stability makes ILs very attractive optical solvents that may be used for the absorption and fluorescence studies of dissolved substances, as well as for monitoring the reactions... [Pg.295]

Many of the fiindamental physical and chemical processes at surfaces and interfaces occur on extremely fast time scales. For example, atomic and molecular motions take place on time scales as short as 100 fs, while surface electronic states may have lifetimes as short as 10 fs. With the dramatic recent advances in laser tecluiology, however, such time scales have become increasingly accessible. Surface nonlinear optics provides an attractive approach to capture such events directly in the time domain. Some examples of application of the method include probing the dynamics of melting on the time scale of phonon vibrations [82], photoisomerization of molecules [88], molecular dynamics of adsorbates [89, 90], interfacial solvent dynamics [91], transient band-flattening in semiconductors [92] and laser-induced desorption [93]. A review article discussing such time-resolved studies in metals can be found in... [Pg.1296]

Other solubilization and partitioning phenomena are important, both within the context of microemulsions and in the absence of added immiscible solvent. In regular micellar solutions, micelles promote the solubility of many compounds otherwise insoluble in water. The amount of chemical component solubilized in a micellar solution will, typically, be much smaller than can be accommodated in microemulsion fonnation, such as when only a few molecules per micelle are solubilized. Such limited solubilization is nevertheless quite useful. The incoriDoration of minor quantities of pyrene and related optical probes into micelles are a key to the use of fluorescence depolarization in quantifying micellar aggregation numbers and micellar microviscosities [48]. Micellar solubilization makes it possible to measure acid-base or electrochemical properties of compounds otherwise insoluble in aqueous solution. Micellar solubilization facilitates micellar catalysis (see section C2.3.10) and emulsion polymerization (see section C2.3.12). On the other hand, there are untoward effects of micellar solubilization in practical applications of surfactants. Wlren one has a multiphase... [Pg.2592]

The most recently introduced optical teclmique is based on the retardation of light guided in an optical waveguide when biomolecules of a polarizability different from that of the solvent they displace are adsorbed at the waveguide surface (optical waveguide lightmode spectroscopy, OWLS) [H]. It is even more sensitive than ellipsometry, and the mode... [Pg.2838]

Similarly, tlie most rapid relaxation metliod, temperature jumping by solvent absorjition of a brief pulse of optical... [Pg.2946]

Much of chemistry occurs in the condensed phase solution phase ET reactions have been a major focus for theory and experiment for the last 50 years. Experiments, and quantitative theories, have probed how reaction-free energy, solvent polarity, donor-acceptor distance, bridging stmctures, solvent relaxation, and vibronic coupling influence ET kinetics. Important connections have also been drawn between optical charge transfer transitions and thennal ET. [Pg.2974]

There have been some attempts to compute nonlinear optical properties in solution. These studies have shown that very small variations in the solvent cavity can give very large deviations in the computed hyperpolarizability. The valence bond charge transfer (VB-CT) method created by Goddard and coworkers has had some success in reproducing solvent effect trends and polymer results (the VB-CT-S and VB-CTE forms, respectively). [Pg.259]

The 7, i5-unsaturated alcohol 99 is cyclized to 2-vinyl-5-phenyltetrahydro-furan (100) by exo cyclization in aqueous alcohol[124]. On the other hand, the dihydropyran 101 is formed by endo cyclization from a 7, (5-unsaturated alcohol substituted by two methyl groups at the i5-position. The direction of elimination of /3-hydrogen to give either enol ethers or allylic ethers can be controlled by using DMSO as a solvent and utilized in the synthesis of the tetronomycin precursor 102[125], The oxidation of the optically active 3-alkene-l,2-diol 103 affords the 2,5-dihydrofuran 104 in high ee. It should be noted that /3-OH is eliminated rather than /3-H at the end of the reac-tion[126]. [Pg.35]

Transparent solid samples can be analyzed directly by placing them in the IR beam. Most solid samples, however, are opaque and must be dispersed in a more transparent medium before recording a traditional transmission spectrum. If a suitable solvent is available, then the solid can be analyzed by preparing a solution and analyzing as described earlier. When a suitable solvent is not available, solid samples may be analyzed by preparing a mull of the finely powdered sample with a suitable oil. Alternatively, the powdered sample can be mixed with KBr and pressed into an optically transparent pellet. [Pg.394]

Thermospray interface. Provides liquid chromatographic effluent continuously through a heated capillary vaporizer tube to the mass spectrometer. Solvent molecules evaporate away from the partially vaporized liquid, and analyte ions are transmitted to the mass spectrometer s ion optics. The ionization technique must be specified, e.g., preexisting ions, salt buffer, filament, or electrical discharge. [Pg.433]

A varnish is often appHed on top of the paint layers. A varnish serves two purposes as a protective coating and also for an optical effect that enriches the colors of the painting. A traditional varnish consists of a natural plant resin dissolved or fused in a Hquid for appHcation to the surface (see Resins, natural). There are two types of varnish resins hard ones, the most important of which is copal, and soft ones, notably dammar and mastic. The hard resins are fossil, and to convert these to a fluid state, they are fused in oil at high temperature. The soft resins dissolve in organic solvents, eg, turpentine. The natural resin varnishes discolor over time and also become less soluble, making removal in case of failure more difficult (see Paint and FINNISH removers). Thus the use of more stable synthetic resins, such as certain methacrylates and cycHc ketone resins, has become quite common, especially in conservation practice. [Pg.420]

Organic Dye Lasers. Organic dye lasers represent the only weU-developed laser type in which the active medium is a Hquid (39,40). The laser materials are dyestuffs, of which a common example is rhodamine 6G [989-38-8]. The dye is dissolved in very low concentration in a solvent such as methyl alcohol [67-56-17, CH OH. Only small amounts of dye are needed to produce a considerable effect on the optical properties of the solution. [Pg.8]

The polyamides are soluble in high strength sulfuric acid or in mixtures of hexamethylphosphoramide, /V, /V- dim ethyl acetam i de and LiCl. In the latter, compHcated relationships exist between solvent composition and the temperature at which the Hquid crystal phase forms. The polyamide solutions show an abmpt decrease in viscosity which is characteristic of mesophase formation when a critical volume fraction of polymer ( ) is exceeded. The viscosity may decrease, however, in the Hquid crystal phase if the molecular ordering allows the rod-shaped entities to gHde past one another more easily despite the higher concentration. The Hquid crystal phase is optically anisotropic and the texture is nematic. The nematic texture can be transformed to a chiral nematic texture by adding chiral species as a dopant or incorporating a chiral unit in the main chain as a copolymer (30). [Pg.202]


See other pages where Optical solvent is mentioned: [Pg.397]    [Pg.397]    [Pg.180]    [Pg.397]    [Pg.397]    [Pg.180]    [Pg.268]    [Pg.57]    [Pg.403]    [Pg.887]    [Pg.890]    [Pg.1179]    [Pg.1249]    [Pg.2595]    [Pg.2841]    [Pg.2966]    [Pg.2976]    [Pg.1081]    [Pg.1014]    [Pg.429]    [Pg.163]    [Pg.693]    [Pg.208]    [Pg.251]    [Pg.251]    [Pg.192]    [Pg.252]    [Pg.281]    [Pg.377]    [Pg.377]    [Pg.328]    [Pg.399]    [Pg.439]    [Pg.12]    [Pg.27]    [Pg.203]    [Pg.359]    [Pg.480]    [Pg.237]    [Pg.249]   
See also in sourсe #XX -- [ Pg.50 ]




SEARCH



Metal solutions in nonaqueous solvents optical spectra

Microscopy, optical solvent casting

Nonlinear optical solvent effects

Optical activity solvent effects

Optical rotation solvent effects

Optical rotatory dispersion , solvent

Optical rotatory dispersion , solvent effects

Optical spectroscopy solvent affects

Optically active solvent

Optically active solvents, spectral effect

Solvent Effect and Aromatic Compounds Magneto-Optic Properties

Solvent effects Raman optical activity

Solvent effects optical calorimetry

Solvent optical permittivity

Solvent optical properties

Solvents, acidic optically active compounds

Spectrum, optical solvent

© 2024 chempedia.info