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Intensity planes

Fig. 8. Generation of the form of the helical diffraction pattern. (A) shows that a continuous helical wire can be considered as a convolution of one turn of the helix and a set of points (actually three-dimensional delta-functions) aligned along the helix axis and separated axially by the pitch P. (B) shows that a discontinuous helix (i.e., a helical array of subunits) can be thought of as a product of the continuous helix in (A) and a set of horizontal density planes spaced h apart, where h is the subunit axial translation as in Fig. 7. This discontinuous set of points can then be convoluted with an atom (or a more complicated motif) to give a helical polymer. (C)-(F) represent helical objects and their computed diffraction patterns. (C) is half a turn of a helical wire. Its transform is a cross of intensity (high intensity is shown as white). (D) A full turn gives a similar cross with some substructure. A continuous helical wire has the transform of a complete helical turn, multiplied by the transform of the array of points in the middle of (A), namely, a set of planes of intensity a distance n/P apart (see Fig. 7). This means that in the transform in (E) the helix cross in (D) is only seen on the intensity planes, which are n/P apart. (F) shows the effect of making the helix in (E) discontinuous. The broken helix cross in (E) is now convoluted with the transform of the set of planes in (B), which are h apart. This transform is a set of points along the meridian of the diffraction pattern and separated by m/h. The resulting transform in (F) is therefore a series of helix crosses as in (E) but placed with their centers at the positions m/h from the pattern center. (Transforms calculated using MusLabel or FIELIX.)... Fig. 8. Generation of the form of the helical diffraction pattern. (A) shows that a continuous helical wire can be considered as a convolution of one turn of the helix and a set of points (actually three-dimensional delta-functions) aligned along the helix axis and separated axially by the pitch P. (B) shows that a discontinuous helix (i.e., a helical array of subunits) can be thought of as a product of the continuous helix in (A) and a set of horizontal density planes spaced h apart, where h is the subunit axial translation as in Fig. 7. This discontinuous set of points can then be convoluted with an atom (or a more complicated motif) to give a helical polymer. (C)-(F) represent helical objects and their computed diffraction patterns. (C) is half a turn of a helical wire. Its transform is a cross of intensity (high intensity is shown as white). (D) A full turn gives a similar cross with some substructure. A continuous helical wire has the transform of a complete helical turn, multiplied by the transform of the array of points in the middle of (A), namely, a set of planes of intensity a distance n/P apart (see Fig. 7). This means that in the transform in (E) the helix cross in (D) is only seen on the intensity planes, which are n/P apart. (F) shows the effect of making the helix in (E) discontinuous. The broken helix cross in (E) is now convoluted with the transform of the set of planes in (B), which are h apart. This transform is a set of points along the meridian of the diffraction pattern and separated by m/h. The resulting transform in (F) is therefore a series of helix crosses as in (E) but placed with their centers at the positions m/h from the pattern center. (Transforms calculated using MusLabel or FIELIX.)...
In Figures 6.17, 6.18, and 6.19 are presented pairs of diffraction intensity planes for three different protein crystals. From two photographs such as these, which are usually (e.g., Figure 6.19) orthogonal to one another, the symmetry of the entire three-dimensional diffraction pattern may be deduced. In some cases, however, additional diffraction images... [Pg.144]

A great deal of research effort has been devoted to studying the effects of sound fields on heat transfer from horizontal cylinders to air. Intense plane sound fields of the progressive or... [Pg.834]

Q is in the direction perpendicular to the equal-intensity planes of the XSW and has a magnitude that is the reciprocal of D. Thus, Q is also referred to as the standing wave vector. [Pg.222]

The g values and spin intensities of specimens from each context showed substantial variation, revealing that a range of carbonization conditions were experienced by kernels even when they were depositied together in a single feature. Figures 3 and 4 shows the data from ancient samples, in the form of plots which place each sample in the g value/intensity plane. The data are superimposed on plots of the standards that were prepared in evacuated, sealed tubes. Midden samples had all been recovered by flotation. The pit samples that were recovered by flotation are distinguished in Figure 4 from those that were recovered without use of flotation. [Pg.157]

Figure 3. Data from ancient maize samples recovered from middens, plotted on a g value / intensity plane. Data from heating in evacuated sealed tubes are included for reference. Figure 3. Data from ancient maize samples recovered from middens, plotted on a g value / intensity plane. Data from heating in evacuated sealed tubes are included for reference.
Figure 5 The modification of intensity of one of the central points of the hole images vs. the distance between the plane of discontinuities and the plane of the holograph... Figure 5 The modification of intensity of one of the central points of the hole images vs. the distance between the plane of discontinuities and the plane of the holograph...
Measuring the electron emission intensity from a particular atom as a function of V provides the work function for that atom its change in the presence of an adsorbate can also be measured. For example, the work function for the (100) plane of tungsten decreases from 4.71 to 4.21 V on adsorption of nitrogen. For more details, see Refs. 66 and 67 and Chapter XVII. Information about the surface tensions of various crystal planes can also be obtained by observing the development of facets in field ion microscopy [68]. [Pg.301]

Additional mfomiation about the vibration ean be obtained tln-ough the depolarization ratio. This is the ratio of the intensity of seattered light that is polarized in a plane perpendieular to the ineident radiation relative to that the seattered light that is polarized parallel to the ineident polarization, p For totally synnnetrie... [Pg.1160]

Figure Bl.6.10 Energy-loss spectrum of 3.5 eV electrons specularly reflected from benzene absorbed on the rheniiun(l 11) surface [H]. Excitation of C-H vibrational modes appears at 100, 140 and 372 meV. Only modes with a changing electric dipole perpendicular to the surface are allowed for excitation in specular reflection. The great intensity of the out-of-plane C-H bending mode at 100 meV confimis that the plane of the molecule is parallel to the metal surface. Transitions at 43, 68 and 176 meV are associated with Rli-C and C-C vibrations. Figure Bl.6.10 Energy-loss spectrum of 3.5 eV electrons specularly reflected from benzene absorbed on the rheniiun(l 11) surface [H]. Excitation of C-H vibrational modes appears at 100, 140 and 372 meV. Only modes with a changing electric dipole perpendicular to the surface are allowed for excitation in specular reflection. The great intensity of the out-of-plane C-H bending mode at 100 meV confimis that the plane of the molecule is parallel to the metal surface. Transitions at 43, 68 and 176 meV are associated with Rli-C and C-C vibrations.
The other type of x-ray source is an electron syncluotron, which produces an extremely intense, highly polarized and, in the direction perpendicular to the plane of polarization, highly collimated beam. The energy spectrum is continuous up to a maximum that depends on the energy of the accelerated electrons, so that x-rays for diffraction experiments must either be reflected from a monochromator crystal or used in the Laue mode. Whereas diffraction instruments using vacuum tubes as the source are available in many institutions worldwide, there are syncluotron x-ray facilities only in a few major research institutions. There are syncluotron facilities in the United States, the United Kingdom, France, Genuany and Japan. [Pg.1378]

If the detection system is an electronic, area detector, the crystal may be mounted with a convenient crystal direction parallel to an axis about which it may be rotated under tlie control of a computer that also records the diffracted intensities. Because tlie orientation of the crystal is known at the time an x-ray photon or neutron is detected at a particular point on the detector, the indices of the crystal planes causing the diffraction are uniquely detemiined. If... [Pg.1379]

Equation (B 1,9.11) is valid only for plane polarized light. For unpolarized incident light, the beam can be resolved into two polarized components at right angles to each other. The scattered intensity can thus be expressed as (figure Bl.9.2)... [Pg.1388]

The extension of the voxel in a radial direction gives infomiation on the lateral resolution. Since the lateral resolution has so far not been discussed in temis of the point spread function for the conventional microscope, it will be dealt with here for both conventional and confocal arrangements [13]. The radial intensity distribution in the focal plane (perpendicular to the optical axis) in the case of a conventional microscope is given by... [Pg.1670]

The polarization dependence of the photon absorbance in metal surface systems also brings about the so-called surface selection rule, which states that only vibrational modes with dynamic moments having components perpendicular to the surface plane can be detected by RAIRS [22, 23 and 24]. This rule may in some instances limit the usefidness of the reflection tecluiique for adsorbate identification because of the reduction in the number of modes visible in the IR spectra, but more often becomes an advantage thanks to the simplification of the data. Furthenuore, the relative intensities of different vibrational modes can be used to estimate the orientation of the surface moieties. This has been particularly useful in the study of self-... [Pg.1782]

Figure Bl.22.10. Carbon K-edge near-edge x-ray absorption (NEXAFS) speetra as a fiinotion of photon ineidenee angle from a submonolayer of vinyl moieties adsorbed on Ni(lOO) (prepared by dosing 0.2 1 of ethylene on that surfaee at 180 K). Several eleetronie transitions are identified in these speetra, to both the pi (284 and 286 eV) and the sigma (>292 eV) imoeeupied levels of the moleeule. The relative variations in the intensities of those peaks with ineidenee angle ean be easily eonverted into adsorption geometry data the vinyl plane was found in this ease to be at a tilt angle of about 65° from the surfaee [71], Similar geometrieal detenninations using NEXAFS have been earried out for a number of simple adsorbate systems over the past few deeades. Figure Bl.22.10. Carbon K-edge near-edge x-ray absorption (NEXAFS) speetra as a fiinotion of photon ineidenee angle from a submonolayer of vinyl moieties adsorbed on Ni(lOO) (prepared by dosing 0.2 1 of ethylene on that surfaee at 180 K). Several eleetronie transitions are identified in these speetra, to both the pi (284 and 286 eV) and the sigma (>292 eV) imoeeupied levels of the moleeule. The relative variations in the intensities of those peaks with ineidenee angle ean be easily eonverted into adsorption geometry data the vinyl plane was found in this ease to be at a tilt angle of about 65° from the surfaee [71], Similar geometrieal detenninations using NEXAFS have been earried out for a number of simple adsorbate systems over the past few deeades.

See other pages where Intensity planes is mentioned: [Pg.344]    [Pg.101]    [Pg.482]    [Pg.488]    [Pg.1042]    [Pg.488]    [Pg.421]    [Pg.425]    [Pg.344]    [Pg.101]    [Pg.482]    [Pg.488]    [Pg.1042]    [Pg.488]    [Pg.421]    [Pg.425]    [Pg.40]    [Pg.379]    [Pg.490]    [Pg.656]    [Pg.658]    [Pg.662]    [Pg.662]    [Pg.666]    [Pg.299]    [Pg.712]    [Pg.978]    [Pg.1138]    [Pg.1379]    [Pg.1381]    [Pg.1525]    [Pg.1573]    [Pg.1579]    [Pg.1658]    [Pg.1664]    [Pg.1668]    [Pg.1669]    [Pg.1806]    [Pg.1807]    [Pg.1820]   
See also in sourсe #XX -- [ Pg.143 , Pg.144 ]




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Diffraction intensity planes

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