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Strain centers

FIGURE 9 Schematic representation of the effect of microstrain defined as the modification of an ideally equidistant lattice (top) by uniform (unidirectional) strain (center) or nonuniform strain (2-D) (bottom). Note the different effects on the diffraction line. [Pg.294]

Fig. 2 Examples for EM that (i) show oxidation of the carbon backbone (left) [12], (ii) possess ring or cage strain (center) [13], or (iii) have very high positive heats of formation (right) [14]... Fig. 2 Examples for EM that (i) show oxidation of the carbon backbone (left) [12], (ii) possess ring or cage strain (center) [13], or (iii) have very high positive heats of formation (right) [14]...
As already mentioned, the first-order Raman signals do not distinguish local strains, so only one signal for the whole wire or dot can be obtained, which consists of the signals of the strained center as well as the relaxed edges. However, even in the first-order spectra, the strain relaxation can be observed as a shift of the LO-phonon frequency toward the value of the unstrained material. The amount of this shift depends on the ratio of the relaxed edges to the strained wire center and, therefore, on the wire width and length [218-222]. [Pg.535]

Stagnation. Large strain center but nonhomogeneous. Birefringence. Opposed nozzles low n, convenience wide range of e. Wall effects (e.g., shear). Lubricant. Stability of flow... [Pg.332]

Speculation about the stability of Ceo centered on the extent to which the aromaticity associated with its 20 benzene rings is degraded by their non planarity and the accompanying angle strain It is now clear that Ceo is a relatively reactive substance reacting with many substances toward which ben zene itself is inert Many of these reactions are char acterized by addition to buckminsterfullerene converting sp hybridized carbons to sp hybridized ones and reducing the overall strain... [Pg.437]

Gonorrhea. Gonorrhea, caused by Neisseriagonorrheae is the most commonly reported communicable disease in the United States. Approximately lO cases were reported to the Center for Disease Control (CDC) in 1979, but actual cases could be two to three times higher (99,100). In addition, an increasing number of strains are becoming resistant to penicillin, the antibiotic that is usually used to treat this disease. [Pg.360]

Malaria affects an estimated 270 million people and causes 2—3 million deaths annually, approximately one million of which occur in children under the age of five. While primarily an affliction of the tropics and subtropics, it has occurred as far north as the Arctic Circle. The disease essentially has been eradicated in most temperate-zone countries, but some 1100 cases of malaria in U.S. citizens returning from abroad were reported to the Centers for Disease Control during 1990. Malaria is seen today in Southeast Asia, Africa, and Central and South America. It is on the increase in Afghanistan, Brazil, China, India, Mexico, the Philippines, Sri Lanka, Thailand, and Vietnam. Escalation of the disease is because of the discontinued use of the insecticide DDT which effectively kills mosquito larvae, but has been found to be toxic to Hvestock and wildlife. Also, chloroquine (6), a reUable dmg for the prophylaxis and treatment of falcipamm malaria, is ineffective in many parts of the world because of the spread of dmg-resistant strains. [Pg.270]

Chelation itself is sometimes useful in directing the course of synthesis. This is called the template effect (37). The presence of a suitable metal ion facihtates the preparation of the crown ethers, porphyrins, and similar heteroatom macrocycHc compounds. Coordination of the heteroatoms about the metal orients the end groups of the reactants for ring closure. The product is the chelate from which the metal may be removed by a suitable method. In other catalytic effects, reactive centers may be brought into close proximity, charge or bond strain effects may be created, or electron transfers may be made possible. [Pg.393]

Conversely, processes which convert carbons to sfp- carbons are more favorable for five-membered than for six-membered rings. This can be illustrated by the data for acetolysis of cyclopentyl versus cyclohexyl tosylate. The former proceeds with an enthalpy of activation about 3kcal/mol less than the latter." A molecular mechanics analysis found that the difference was largely accounted for by the relief of torsional strain in the cyclopentyl case." Notice that there is an angle-strain effect which is operating in the opposite direction, since there will be some resistance to the expansion of the bond angle at the reaction center to 120° in the cyclopentyl ring. [Pg.172]

If Cm -I- 3Cii > 0, a centered simple wave will be produced by impact loading, and a record of this waveform suffices to determine the entire uniaxial stress-strain relation over the range of strains encountered. Vitreous silica is a material responding in this manner, and its coefficients have been determined by Barker and Hollenbach [70B01] (see also [72G02]) on the basis of a simple-wave analysis. [Pg.23]

As an explanation of the preferred formation of pyrrolidines as compared to lower and higher membered heterocyclic rings, the necessity of a nearly linear arrangement of the involved centers in the hydrogen transfer step and a minimum of nonclassical strain in a cyclic 6-membered chair-like intermediate was postulated although the experimental evidence is not conclusive. [Pg.257]

Diels-Alder reaction and. 494-495 El reaction and, 392 E2 reaction and, 387-388 R.S configuration and, 297-300 S 1 reaction and, 374-375 S -2 reactions and, 363-364 Stereogenic center, 292 Stereoisomers, 111 kinds of, 310-311 number of, 302 properties of, 306 Stereospecilic, 228, 494 Stereospecific numbering, sn-glycerol 3-phosphate and, 1132 Steric hindrance, Sjvj2 reaction and, 365-366 Steric strain, 96... [Pg.1315]


See other pages where Strain centers is mentioned: [Pg.471]    [Pg.294]    [Pg.98]    [Pg.461]    [Pg.471]    [Pg.294]    [Pg.98]    [Pg.461]    [Pg.548]    [Pg.1186]    [Pg.250]    [Pg.87]    [Pg.543]    [Pg.545]    [Pg.546]    [Pg.98]    [Pg.115]    [Pg.217]    [Pg.237]    [Pg.187]    [Pg.461]    [Pg.385]    [Pg.514]    [Pg.259]    [Pg.218]    [Pg.191]    [Pg.130]    [Pg.274]    [Pg.8]    [Pg.102]    [Pg.112]    [Pg.23]    [Pg.97]    [Pg.779]    [Pg.1186]    [Pg.95]    [Pg.193]    [Pg.107]    [Pg.832]    [Pg.428]    [Pg.195]   
See also in sourсe #XX -- [ Pg.98 ]




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Substituents at the Radical Center that Induce Allylic Strain

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