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Polarized fight

Light of definite energy and polarization has a selective power to exclusively excite dye molecules whose electronic transition energy and orientation match these parameters. Thus, if a dye is excited by polarized fight, its emission will also be highly polarized. Depolarization occurs only when the time correlation of these selectively excited species is lost due to their rotation or participation in some... [Pg.114]

In many luminescence centers the intensity is a function of a specific orientation in relation to the crystallographic directions in the mineral. Even if a center consists of one atom or ion, such luminescence anisotropy may be produced by a compensating impurity or an intrinsic defect. In the case of cubic crystals this fact does not disrupt optical isotropy since anisotropic centers are oriented statistically uniformly over different crystallographic directions. However, in excitation of luminescence by polarized fight the hidden anisotropy may be revealed and the orientation of centers can be determined. [Pg.4]

The sensitivity of the sensor is usually defined by the change in Nm per change in tic, i.e., dNm/dtic. An expression for this for, say, TE polarized fight can be derived by using perturbational analysis of the mode equation (Eq.2) [16] ... [Pg.284]

Figure 9.22 Traditional Fisher projection of the two glucose sterioisomers—one reflects plane-polarized fight to the right [dextrorotatory (d)] and the other reflects it to the left [levorotatory (l)]. Figure 9.22 Traditional Fisher projection of the two glucose sterioisomers—one reflects plane-polarized fight to the right [dextrorotatory (d)] and the other reflects it to the left [levorotatory (l)].
Devices based on lanthanum lead zirconate titanate (PLZT) using polarized fight can be switched from transparent to opaque in microseconds. Welding goggles and aircraft windows offer protection from sudden flashes of intense fight. [Pg.929]

Figure 9 A type B1 inclusion from the Allende CVS chondrite. This centimeter-sized marhle consists mainly of melilite (bluish-white), titanium-aluminum-rich calcic pyroxene (bright colors), and anorthite and spinel (not readily visible in photo). Type B1 inclusions figure prominently in the early petrologic, trace element, and isotopic studies of CAIs, in part because of the richness of information about physicochemical histories available from petrologic, chemical and isotopic properties. Ironically, because type B inclusions occur only in CVS chondrites, they are nonrepresentative of CAIs in general. Photograph taken in cross-polarized transmitted fight. The colors are not the true colors of the crystals they are artifacts of the polarized fight. Figure 9 A type B1 inclusion from the Allende CVS chondrite. This centimeter-sized marhle consists mainly of melilite (bluish-white), titanium-aluminum-rich calcic pyroxene (bright colors), and anorthite and spinel (not readily visible in photo). Type B1 inclusions figure prominently in the early petrologic, trace element, and isotopic studies of CAIs, in part because of the richness of information about physicochemical histories available from petrologic, chemical and isotopic properties. Ironically, because type B inclusions occur only in CVS chondrites, they are nonrepresentative of CAIs in general. Photograph taken in cross-polarized transmitted fight. The colors are not the true colors of the crystals they are artifacts of the polarized fight.
Liquid crystalline fluorene oligomers can emit polarized fight with proper alignment of their molecular axes and, hence, of their transition dipole moments. For example, linearly polarized emission results from uniaxial alignment of fluorene oligomers. One common way to characterize linearly polarized emission is to measure its emission dichroism, viz. the emission... [Pg.163]

The equilibrium and kinetics of the immunochemical reactions have been studied by means of fluorescence quenching and polarization, fight... [Pg.160]

Figure 25-4 Light from a lamp or from the sun consists of electromagnetic waves that vibrate in all directions perpendicular to the direction of travel. Polarizing filters absorb all waves except those that vibrate in a single plane. The third polarizing filter, with a plane of polarization at right angles to the first, absorbs the polarized fight completely. Figure 25-4 Light from a lamp or from the sun consists of electromagnetic waves that vibrate in all directions perpendicular to the direction of travel. Polarizing filters absorb all waves except those that vibrate in a single plane. The third polarizing filter, with a plane of polarization at right angles to the first, absorbs the polarized fight completely.
In addition to tartaric acid another compound named paratartaric acid was found in wine sediments. Chemical analysis showed this compound to have the same composition as tartaric acid, so most scientists assumed the two compounds were identical. Strangely enough, however, paratartaric acid did not rotate plane-polarized fight. Pasteur would not accept the idea that such an experimental result could be an accident or unimportant. He guessed that even though the two compounds had the same chemical composition, they must somehow have different structures—and he set out to find evidence to prove his hypothesis. [Pg.917]

The TT and cr components respond differently to polarized fight. The tt component absorbs fight polarized in the direction parallel to the magnetic field. The cr components... [Pg.420]

The analysis of thin films is often performed by infrared spectroscopy. Compared to reflection absorption measurements on metal surfaces using p-polarized fight at grazing incidence, investigation of self-supported thin films or of thin films on transparent substrates shows weaker infrared absorption bands. Weaker absorption bands are caused by the absence of the surface enhancement mechanism and the poorer reflectivity. On the other hand, due to the absence of the metal selection rule, spectra of p- and s-polarization can be recorded in the case of freestanding films or of transparent substrates. Complex spectral features may arise... [Pg.77]

Occasionally, an optically inactive sample of tartaric acid was obtained. Pasteur noticed that the sodium ammonium salt of optically inactive tartaric acid was a mixture of two mirror-image crystal forms. With microscope and tweezers, Pasteur carefully separated the two. He found that one kind of crystal (in aqueous solution) was dextrorotatory, whereas the mirror-image crystals rotated the plane of polarized fight an equal amount but were levorotatory. [Pg.307]

Pairs of enantiomers such as A- and A-[Cr(acac)3] differ only in their action on polarized fight. However, for ionic complexes such as [Co(en)3] +, there is the opportunity to form salts with a chiral counter-ion A . These salts now contain two different types of chirality the A- or A-chirafity at the metal centre and the (-f) or (—) chirality of the anion. Four combinations are possible of which the pair A-(- -) and A-(—) is enantiomeric as is the pair A-(—) and A-(-l-). However, with a given anion chirality, the pair of salts A-(—) and A-(—) are diastereoisomers... [Pg.630]

A new class of hexabenzocoronene derivatives, e.g. compounds (Scheme 7.13) can self-organize into liquid crystalline phases composed of molecular stacks that orient spontaneously parallel to the surface [177, 178]. Field effect transistors based on these materials show high charge-carrier mobilities, high on/off ratios, and low tum-on voltages. So far compound 44 exhibits the best field effect transistor properties achieved for a columnar discotic material. Polarized fight microscopy revealed that these materials tend to orient their columns parallel to the surface upon thermal annealing. [Pg.239]

We may also determine the relative configuration of chiral structures even though bonds are broken to the chiral center if we are able to determine whether the reaction proceeds with retention or with inversion of configuration. The Sn2 reaction of (S)-(—)-2-chloropropanoic acid (87) with hydroxide ion produces (—)-lactic acid, which must have the R configuration (88, Figure 2.34). Note that in this case the direction of rotation of plane-polarized fight stays the same, even though there has been an inversion of the substituents at the chiral center. [Pg.92]


See other pages where Polarized fight is mentioned: [Pg.503]    [Pg.69]    [Pg.270]    [Pg.41]    [Pg.159]    [Pg.272]    [Pg.81]    [Pg.260]    [Pg.57]    [Pg.75]    [Pg.69]    [Pg.164]    [Pg.580]    [Pg.35]    [Pg.503]    [Pg.328]    [Pg.649]    [Pg.917]    [Pg.976]    [Pg.1281]    [Pg.1329]    [Pg.300]    [Pg.256]    [Pg.304]    [Pg.60]    [Pg.219]    [Pg.212]    [Pg.280]    [Pg.62]    [Pg.927]    [Pg.318]    [Pg.630]    [Pg.3124]    [Pg.113]   
See also in sourсe #XX -- [ Pg.384 , Pg.385 , Pg.866 , Pg.867 ]




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