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Light planar

Fig. 21.3 The crystal structure of BasBPO . The dark tetrahedrons represent [P04] groups the light planar trigons represent [BOs] groups the light spheres represent Ba atoms. Fig. 21.3 The crystal structure of BasBPO . The dark tetrahedrons represent [P04] groups the light planar trigons represent [BOs] groups the light spheres represent Ba atoms.
S. M. Yang, H. Miguez, and G. A. Ozin, Opal circuits of light-planarized microphotonic crystal chips, Adv. Funct Mater., 12, 425-431 [2002]. [Pg.618]

A planar polished surface reflects heat radiation in a similar manner with which it reflects light. Rough surfaces reflect energy in a diffuse manner hence radiation is reflected in all directions. A blackbody absorbs all incoming radiation and therefore has no reflection. A perfect blackbody does not exist a near perfect blackbody surface such as soot reflects 5% of the radiation, making it the standard for an ideal radiator. [Pg.106]

Consider light traveling from one medium to another (Fig. 1). To simplify the problem, we can consider that the media are infinite in extent and that the interface between the media is planar. Note that a more complex geometry will not change the result. Also consider that each medium can be described by an index of refraction, n, which is the apparent speed of the wave through... [Pg.37]

The isomerization takes place because the excited states, both 5i and T, of many alkenes have a perpendicular instead of a planar geometry (p. 311), so cis-trans isomerism disappears upon excitation. When the excited molecule drops back to the So state, either isomer can be formed. A useful example is the photochemical conversion of c/s-cyclooctene to the much less stable trans isomer." Another interesting example of this isomerization involves azo crown ethers. The crown ether (5), in which the N=N bond is anti, preferentially binds NH4, Li, and Na, but the syn isomer preferentially binds and Rb (see p. 105). Thus, ions can be selectively put in or taken out of solution merely by turning a light source on or off." ... [Pg.320]

The classical scheme for dichroism measurements implies measuring absorbances (optical densities) for light electric vector parallel and perpendicular to the orientation of director of a planarly oriented nematic or smectic sample. This approach requires high quality polarizers and planarly oriented samples. The alternative technique [50, 53] utilizes a comparison of the absorbance in the isotropic phase (Dj) with that of a homeotropically oriented smectic phase (Dh). In this case, the apparent order parameter for each vibrational oscillator of interest S (related to a certain molecular fragment) may be calculated as S = l-(Dh/Di) (l/f), where / is the thermal correction factor. The angles of orientation of vibrational oscillators (0) with respect to the normal to the smectic layers may be determined according to the equation... [Pg.210]

It can also be mentioned that polyphosphazenes substituted with aromatic groups, such as phenols or naphthols, can form inter- and intra- molecular excimers by coupling reaction of the planar aromatic rings of the substituents under illumination [467-471,473,725]. These species disappear as soon as the light is switched off. [Pg.224]

Maier and co-workers condensed formaldehyde and elemental silicon at 12 K in an argon matrix and photolyzed the mixture to form silaketene H2SiCO, which is similar in structure to the silylene-CO adduct mentioned above. The reactants first form siloxiranylidene 49 (which equilibrates with an unknown species postulated as the planar/linear silaketene 50 when exposed to 313-nm-wavelength light) and then forms complex 51 when photolyzed at 366 nm (Scheme 15). This species could also be formed by photolyzing diazidosilane 52 in the presence of CO, and complex 51 equilibrates with SiCO (53) and H2. The CO infrared shift for this bent structure was calculated at 2129 cm , which is shifted —80cm from the calculated value of free CO, at 2210 cm. The experimentally observed value was reported at 2038-2047 cm at 12 K. [Pg.15]

In recent years, high-resolution x-ray diffraction has become a powerful method for studying layered strnctnres, films, interfaces, and surfaces. X-ray reflectivity involves the measurement of the angnlar dependence of the intensity of the x-ray beam reflected by planar interfaces. If there are multiple interfaces, interference between the reflected x-rays at the interfaces prodnces a series of minima and maxima, which allow determination of the thickness of the film. More detailed information about the film can be obtained by fitting the reflectivity curve to a model of the electron density profile. Usually, x-ray reflectivity scans are performed with a synchrotron light source. As with ellipsometry, x-ray reflectivity provides good vertical resolution [14,20] but poor lateral resolution, which is limited by the size of the probing beam, usually several tens of micrometers. [Pg.247]


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