Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Electron patterns

It is seen how all indicators of aromaticity correctly predict that a structure close to the TS is the most aromatic species along the reaction path, except HOMA and FLU indices, that are unsuccessful to account for the aromaticity of the TS. The reason for the failure of HOMA and FLU is that both values measure variances of the structural and electronic patterns, respectively, with respect to a reference value. Therefore, HOMA and FLU might fail if they are not applied to stable species because, while reactions are occurring, structural and electronic parameters suffer major changes. It is worth noting that the isotropic NICS(O) and NICS(l) values of the TSs are larger than those of benzene, but this is not the case with the more sophisticated NICS indices. [Pg.429]

It should be emphasized that this analysis is based on the assumption of some appreciable 2—5 overlap in all-c/s and cis-gauche 1,3,5-hexatriene. Furthermore, it should be pointed out that our analysis of the conformational preference of 1,3,5-hexatriene is aiming at revealing electronic patterns. In reality, the all-c/s conformation of 1,3,5-hexatriene is unfavorable due to repulsive interactions between the two methylene groups, i.e. conformational preference varies in the order all-frans > cis-gauche. [Pg.31]

Exposure tools Gamma radiation from 60Co source Flood exposure to 50 keV electrons Pattern exposure to 20 keV electrons... [Pg.325]

Both the physical properties and the knocking characteristics of pure hydrocarbons seem to reflect minor changes in the valence electron pattern of the molecule. [Pg.366]

The typical shapes of the electron patterns determine the specific properties of atoms. For example, in the oxygen atom the electrons fill the lowest patterns up to the fourth one. The resulting pattern combination is characteristic for oxygen and is responsible for its properties it determines how oxygen combines with other atoms (forming water with hydrogen, for example) and how the atoms fall into a symmetrical crystalline order when they form solids, such as ice crystals. [Pg.1394]

The electron patterns are the primal shapes of nature. Fundamentally, all of nature s shapes can be traced to such patterns. Even the properties of living substances are based on them—in particular, the properties of the molecules that carry the hereditary code. In the final scientific analysis, the stability of electron wave patterns causes the same flowers to bloom every spring and makes children similar to their parents. [Pg.1394]

The space left behind by the loss of an electron is known as a positive hole. The negative iodide ion and the positive hole in the polyacetylene chain associated with it is known as a polaron. A disturbance of this kind may then lead to a disruption of electron patterns in nearby portions of the molecule, resulting in a reversal of single and double bonds, producing a pattern known as a soliton. The now... [Pg.166]

New promising technologies for future electron-beam lithography applications based on pyroelectrically induced electron emission from LiNbOs ferroelectrics [22] were recently proposed [23], The developed system possessing micrometer scale resolution used 1 1 electron beam projection. The needed electron pattern was obtained by means of deposited micrometer-size Ti-spots on the polar face of LiNbOs. Another solution for the high resolution electron lithography may be found in nanodomain patterning of a ferroelectric template. [Pg.192]

Behl M, Seekamp J, Zankovych S, Torres CMS, Zentel R and Ahopelto J, Towards plastic electronics Patterning semiconducting polymers by nanoimprint lithography , Adv Mater, 2002 14 588-591. [Pg.268]

The strength of this attraction is based on two factors the distance from the nucleus to the outermost electrons, and the valence electron pattern. The distance factor is a function of the fact that the closer the nucleus is to the outer electrons, the greater the power of the nucleus in pulling in other electrons. This is similar to the observation that a magnet works best when close to an object. As the valence electron pattern approaches the noble gas valence electron pattern, the more effective the element is at attracting electrons. Noble gases have virtually no electronegativity, as they rarely react. [Pg.121]

Se, S, Cl. Se has the lowest electronegativity because it has the largest atomic size, meaning that its nucleus is farther from the outer electrons. Chlorine is closer to having the noble gas valence electron pattern than is sulfur. [Pg.122]

Because sodium and potassium both have the same valence electron pattern, with s it must be the distance factor that is important. [Pg.122]

Nonmetals have higher electronegativity because they are gainers of electrons, this being their best pathway to achieving a noble gas valence electron pattern. [Pg.122]

An electron diffraction study of the ordered nanocrystalline entities demonstrated that the electron patterns were similar to those of block crystals. As distinct from the block crystals, the ordered nanocrystalline entities had discontinuities (Fig. 2a). The electron patterns of the ordered nanocrystalline entities suggested a high orientation coordination of their constituent nanocrystallites (Fig. 2b). [Pg.569]

Pharmacophore Models. It is often useful to assume that the receptor site is rigid and that structurally different drugs bind in conformations that present a similar steric and electronic pattern, the pharmacophore. Most drugs, because of inherent conformational freedom, are capable of presenting a multitude of three-dimensional patterns to a receptor. The pharmacophoric assumption led to a problem statement that logically is composed of two processes. F irst is the determina-... [Pg.127]

Activity versus Affinity. Given a consistent model of either type, a limitation is that one can only ask whether the compound under consideration can present the three-dimensional electronic pattern (pharmacophore) that is the current candidate. In other words, one is limited to predicting the presence or absence of activity, a binary choice. Even the presence of the appropriate pattern is insufficient to ensure biological activity. For example, competition with the receptor for occupied space by other parts of the molecule can inhibit binding and preclude activity. We can thus postulate the following conditions for activity ... [Pg.131]

In these nitrogen is the donor atom, and in most NO is bound as NO+ which is isoelectronic with CN and CO. The NO group can thus donate one extra electron to the metal this accounts for the stability of Co(NO)(CO)3 which has the same electronic pattern as Ni(CO)4 (p. 494). Co-ordination complexes of this type do not usually contain more than one NO group and they are generally of outer orbital (sp ) type (p. 134). [Pg.328]

FIGURE 5.7 Typical electron pattern from a carbyne crystal flake with rhombohedral form (a) diffraction pattern and (b) transmission electron micrograph. [Pg.90]

Let us now consider the expected hyperconjugative delocalizations in the unique P structure 11b. This electronic pattern immediately suggests that a planar structure may be unfavorable, becanse the formal hole then has no possible donor-acceptor interactions with adjacent donors because of strict G-n separation in this geometry. Twisting about the C-C bond (to break a-n symmetry) is expected to turn on vicinal... [Pg.435]

While the approaches utilizing pyridine derivates often appeared promising on paper, in reality, multiple substitution reactions, complex chemistries, and several important compromises were generally required to install the desired C2-, C3-, C4-, and C5-tetra-substitution pattern and furnish an appropriately functionalized 6-azaindole. A closer look at the electronic pattern for a typical pyridine ring revealed that the C3 and C5 positions are the most difficult to... [Pg.183]

The mass of the electron determines the de Broglie wave-length A = hjinv and so fixes the scale of the quantum phenomena in which it participates. It is because the electron is of small mass that the atom has a radius very many times greater than the nucleus. The electrons being remote, the nucleus may be treated as a point charge with a high degree of approximation, and most of chemistry thus becomes an affair of the electron patterns alone. [Pg.239]

M. Behl, J. Seekamp, S. Zankovych, CM.S. Torres, R. Zentel, and J. Ahopelto, Towards plastic electronics Patterning semiconducting polymers by nanoimprint hthography, Adv. Mater., 14, 588-591 (2002). [Pg.460]

This result should make you feel faint. Why You would like the Moon, a proton or an electron to be solid objects, wouldn t you All investigations made so far indicate that the electron is a point-like elementary particle. If, in the experiments we have considered, the electrons were to be divided into two classes those that went through slit 1 and those that passed slit 2, then the electron patterns would be different. The pattern with the two slits had to be the sum of the patterns corresponding to only one open slit (facing slit 1 and slit 2). We do not have that picture. [Pg.42]


See other pages where Electron patterns is mentioned: [Pg.353]    [Pg.549]    [Pg.364]    [Pg.370]    [Pg.372]    [Pg.200]    [Pg.27]    [Pg.117]    [Pg.121]    [Pg.122]    [Pg.74]    [Pg.317]    [Pg.148]    [Pg.196]    [Pg.586]    [Pg.396]    [Pg.520]    [Pg.317]    [Pg.44]    [Pg.18]    [Pg.201]   
See also in sourсe #XX -- [ Pg.306 , Pg.307 ]

See also in sourсe #XX -- [ Pg.43 ]




SEARCH



Carbon, electron diffraction pattern

Carbon, electron diffraction pattern from

Cellulose electron diffraction pattern

Electron beam patterning

Electron deformation density patterns

Electron diffraction example patterns

Electron diffraction pattern

Electron diffraction pattern analysis

Electron diffraction pattern, mineral

Electron diffraction patterns mordenite crystals

Electron impact fragmentation pattern

Electron microscopy diffraction patterns

Electron spin resonance powder pattern

Electron transfer general reactivity patterns

Electron transfer reactivity patterns

Electron-beam patterning resolution

Electronic Structures and Reactivity Patterns

Electronic pattern preparation, methodology

Electronic speckle pattern

Electronic speckle pattern interferometry

Electronic speckle pattern interferometry ESPI)

Electronic tongues pattern recognition tools

Ferrihydrite electron diffraction pattern

Fragmentation pattern, electron

Interpretation of electron diffraction patterns

Intramolecular electron density pattern

Low energy electron diffraction patterns

Low-energy electron diffraction LEED) patterns

Pattern recognition electronic factors

Pattern recognition electronic nose systems

Patterning, electronic devices

Phase electron diffraction pattern

Poly electron diffraction pattern

Polyethylene electron diffraction patterns

Scanning electron microscopy pattern

Scanning transmission electron microscopy diffraction patterns

Selected area electron diffraction patterns

Specific reactivity patterns in electron-transfer reactions

Transmission electron diffraction pattern

Water cluster electron diffraction pattern

© 2024 chempedia.info