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Spectrum of structure

The scheme of dispersion effects displayed in engineering materials of different structures was considered and an analysis of the causes of their occurrence was performed in our work. The spectrum of structural noise is considered as an element of unified spectral characteristics, reflected interaction of the ultrasonic field with given parameters and heterogeneous medium... [Pg.733]

Parameters measured Surface topography (rms roughness, rms slope, and power spectrum of structure) scattered light line shape of periodic structure (width, side wall angle, height, and period)... [Pg.54]

It is impossible to generalize these properties for such a wide spectrum of structures. Some interesting and/or typical compounds were treated in CHEC-II(1996) and no substantial progress has been reported since. [Pg.378]

The spectrum of structural mutations that can convert a proto-oncogene into an oncogene is very diverse. Both simple amino acids changes in the coded protein and larger structural changes are observed. In particular, viral oncoproteins demonstrate multiple mutations compared to their cellular coimterparts, linked to important and far-reaching structural and fimctional changes. [Pg.429]

Cations come in many shapes and sizes. The simplest is the lone proton which may jump from base to base along a small channel. Then there are inorganic ions with no directional preferences for bonding, such as the alkali or alkaline metals, and NH4+ which is tetrahedral but appears spherical when hydrated. At the other end of the spectrum of structural complexity we have organic cations and hydrated transition metal complexes with non-uniform charge densities. [Pg.163]

A stereospecific synthesis of [6]paracyclophane-8-carboxylic acid (2) was reported, and its CD spectrum was compared with that of [8]paracyclophane-10-carboxylic acid (3, R = CO2H) [17]. The former afforded a pair of bisignate CD patterns in the 200-400 nm region, while only a pair of Cotton effect peaks of the same sign were observed for the latter. The CD intensity (IAsI) of 2 was in the order of 10 M 1 cm4 for the main band at 220 nm. [6]Paracyclophane (2) is one of the most strained cyclophanes, and its boat-type deformation of the benzene ring led to the red-shift of ca. 30 nm in its UV and CD spectra. The theoretical spectrum obtained at the TD-DFT-B3-LYP/TZV2P level well reproduced the experimental spectrum except for the sign of the weak 1Lh band around 320 nm [8]. The CD spectrum of structurally similar methyl 3,6-hexanooxepin-4-carboxylate was also reported [16]. [Pg.103]

Take a moment to review the H spectrum of structure 8-2 (Example 8.11). What would be the effect of irradiating the Hb multiplet at 8 1.76 Saturating spin states of Hb by irradiation at that frequency would cause all H-H spin couplings involving that nucleus to disappear. As a result, the doublet centered at 8 0.915 would collapse to a singlet, and the triplet at 8 3.40 would collapse to a doublet. [Pg.198]

Figure 4.8 A spectrum of structurally diverse factor Xa inhibitors with potencies in the nanomolar range. Figure 4.8 A spectrum of structurally diverse factor Xa inhibitors with potencies in the nanomolar range.
Each of the methods cited yields a measure of average crystallinity, which is really only defined operationally and in which the polymer is assumed artificially to consist of a mixture of perfectly ordered and completely disordered segments. In reality, there will be a continuous spectrum of structures with various degrees of order in the solid material. Average crystallinities determined by the different techniques cannot always be expected to agree very closely, because each method measures a different manifestation of the structural regularities in the solid polymer. [Pg.385]

As work progressed, we desired an acid intermediate that would allow us a broader spectrum of structural variants on the amide nitrogen. We found that the desired vinylogous carbamic acid could be prepared directly from cyanoacetic acid (Figure 5). When R equals (substituted)benzyl, an approximate 1 1 ratio of desired products and decarboxylated products was obtained. When R equals (substituted)phenyl, only the desired carboxylic acid intermediates were obtained. The impure vinylogous carbamic acids could easily be purified by base extraction. These acids were converted to vinylogous ureas via their stable acid chlorides. [Pg.114]

In the 1980s and NMR spectra of the 2-norbomyl cation at substantially higher fields, that is, 395 MHz H and 50 MHz C, have been obtained at similar low temperatures. The 395 MHz ll NMR spectrum of structure of CyHii is fully resolved compared with that previously reported at 100 MHz (Fig. 5.6). [Pg.231]

The spectrum of structural mutations that can convert a proto-oncogene into an oncogene is very diverse. Both simple amino acid changes and larger structural... [Pg.479]

Two issues deserve comment. First, there is as yet no evidence for clatherate water structures surrounding globular proteins. Second, there is no sharp "boundary" on structural features. The diffraction experiments encourage us to think of a spectrum of structural sites characterized by an order parameter ranging from highly ordered to completely random distribution over two or three layers of water molecules. [Pg.5]

In commercial practice, these distinctions separate most foams into discrete classifications. In theoretical analysis, it is difficult to use a single process to produce a complete spectrum of structures, and it is difficult to relate properties to the complete spectrum of structure in a single unambiguous homologous series. It is hoped that such continuous analysis will be more feasible in the future. [Pg.474]


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See also in sourсe #XX -- [ Pg.302 ]




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