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Electrons relating

The most likely CVD applications of these superconductors to reach the practical stage are coatings for semiconductor and other electronic-related applications. For 1 arger current-carrying applications, a superconductor coating over a metallic conductor such as copper may also become a practical design because of its advantage over a monolithic superconductor wire. It is able to handle current excursions and has better mechanical properties. [Pg.379]

Electronically related to such borirenes are the salts of the dianion of 1,2-di-tert-butyl-3-[bis(trimethylsilyl)]methyl]-l, 2-diborirane.85 An XRD analysis of the dipotassium salt (86a,b) uncovered shortened B—B (1.58 A) and B—C (1.50 A) bonds, as suggested by resonance contributions 86a and 86b. Salt 86 can be considered to have largely a 2- r-electron Hiickel aromatic ring. [Pg.378]

Larock extended this Pd-catalyzed diene heteroannulation to other dienes and anilines [399], including functionalized dienes leading to, for example, ketotetrahydrocarbazoles [400]. Back has employed 1-sulfonyl-l,3-dienes in this 2-vinylindoline synthesis [401], and the use of 1,3-dienes in constructing indolines has been adapted to the solid phase by Wang [402]. Interestingly, Larock has shown that the electronically-related vinylcyclopropanes undergo a similar cyclization with o-iodoanilines to form 2-vinylindolines, e.g., 310 [403, 404]. Vinylcyclobutane also reacts in a comparable manner. [Pg.145]

As indicated in Scheme 11, there are basically two classes of chemistry that have been observed for [Os CO) ]2-. One involves expansion of the ligand coordination sphere, without changing the stereochemistry of the metal cluster, and is electronically related to the parent carbonyl Os5(CO)18, while the second involves redox reactions, with addition of two electrons to the metal cluster and concomitant structural changes in the metal polyhedra (204). [Pg.328]

Semiempirical methods are widely used, based on zero differential overlap (ZDO) approximations which assume that the products of two different basis functions for the same electron, related to different atoms, are equal to zero [21]. The use of semiempirical methods, like MNDO, ZINDO, etc., reduces the calculations to about integrals. This approach, however, causes certain errors that should be compensated by assigning empirical parameters to the integrals. The limited sets of parameters available, in particular for transition metals, make the semiempirical methods of limited use. Moreover, for TM systems the self-consistent field (SCF) procedures are hardly convergent because atoms with partly filled d shells have many... [Pg.681]

O Anthony Garofalo, "Housing Electrons Relating Quantum Numbers, Energy Levels, and Electron Configurations," J. Chem. [Pg.183]

As a conducting polymer, polyaniline has many electronics-related applications, such as rechargeable batteries (Tsutsumi et al. 1995), multilayer heterostructure light-emitting diode devices (Onoda Yoshino 1995), biosensors (Bartlett Whitaker 1987), elec-trochromic windows (Nguyen Dao 1989), and nonlinear optical materials (Papacostadi-nou Theophilou 1991). Polyaniline may be prepared from aniline by both electrochemi-... [Pg.237]

These cross-referenced numbers are the key to the electronic relational data bases. Key field data and sample storage data are entered into location and sample number files in QUIZ Software (4). Laboratory analysis information is contained in files generated using Perkin-Elmer Laboratory Information Management System (LIMS) and Chromatographic Laboratory Analysis System (CLAS) software. [Pg.64]

Another group of unstable carbanions are those with antiaromatic character (Scheme 5.71). Thus, cyclopropenyl anions or oxycyclobutadienes, generated by deprotonation of cyclopropenes or cyclobutenones, respectively, will be highly reactive and will tend to undergo unexpected side reactions. Similarly, cyclopentenediones are difficult to deprotonate and alkylate, because the intermediate enolates are electronically related to cyclopentadienone and thus to the antiaromatic cyclopenta-dienyl cation. [Pg.196]

The effect of long-range electron transfer on chemiluminescence of the hexanuclear cluster ion Mo6Cl f in the presence of three series of structurally and electronically related organic compounds (aromatic amine radical cations A+, nitroaromatic... [Pg.23]

A magnetic field will give rise to tensorial properties for electron-related phenomena... [Pg.45]

In (10), an additional factor 2 accounts for the two symmetrical diagrams Fig. 1, (c) and (e). In these equations, Sp(x,y E)y0 denotes the time-independent Green function of a bound electron related to the four-dimensional electron propagator by... [Pg.609]

This takes us back to the total TF energy in equation (20). When we consider again the basis of this, we note first that the kinetic energy density tr has been approximated by equation (18), which is a local free electron relation. Formally, it is straightforward to take the variation of T— J tr dr with respect to p, and then one can write the Euler equation (24) in the generalized form... [Pg.102]

The spin angular momentum of an electron is properly described by a three-component vector and an isolated spin is free to orient in any direction in space. Likewise, the magnetic moment of the electron, related to the vector spin through the relation... [Pg.2478]

If the constant electron transfer feature is real, we would expect to find similar effects in electronically related nonnoble gas compounds. Consider, for example, the formation of the halogen fluorides. The centr atom of the monofluorides can be thought of as a pseudo-rare-gas atom and the subsequent formation of the trifluorides and pentafluorides via a three-center bonding scheme is analogous to the formation of rare gas difluorides and tetrafluorides. If the constant electron transfer is due to independence of the perpendicular, three-center bonds, we could expect the two equivalent fluorines in BrFs each to have the same charge as each of the four equivalent fluorines in BrFs. The X-ray photoelectron spectra of these molecules have been measured in this laboratory and are currently being analyzed. Finally, it is known that the thermo-... [Pg.115]


See other pages where Electrons relating is mentioned: [Pg.36]    [Pg.137]    [Pg.239]    [Pg.98]    [Pg.246]    [Pg.97]    [Pg.240]    [Pg.141]    [Pg.260]    [Pg.238]    [Pg.43]    [Pg.860]    [Pg.251]    [Pg.253]    [Pg.253]    [Pg.860]    [Pg.262]    [Pg.610]    [Pg.360]    [Pg.13]    [Pg.77]    [Pg.8]    [Pg.117]    [Pg.120]    [Pg.255]    [Pg.305]    [Pg.1121]    [Pg.3367]    [Pg.51]    [Pg.522]    [Pg.225]    [Pg.133]    [Pg.461]    [Pg.5]   
See also in sourсe #XX -- [ Pg.85 , Pg.86 ]




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Electron affinity, relation

Electron affinity, relation radius

Electron affinity, relation work function

Electron balance relation

Electron dispersion relation

Electron self-exchange reactions Marcus cross relation

Electron tunnelling relation

Electron-pair Approximation and Related Methods

Electron-transfer recurrence relation

Electronic Effects in Metallocenes and Certain Related Systems

Electronic Pressure Relation

Electronic Structure and Relation to Properties

Electronic Work Function and Related Values in Electrochemical Kinetics

Electronic, Electrical and Related Materials

Electrons related molecules

Exciplexes, Electron Donor-Acceptor Complexes, and Related Charge-transfer Phenomena

Fermi level electron related properties, metals

General features relating to stability—filled shells of electrons

How is color related to a transferred electron

Many-electron systems relations

Photonics, electronics and related applications

Potential Energy Surfaces for Ground-State Electron Transfer. Relation to Photochemistry Nonadiabatic Chemistry

Potential Relation for Electron Transfer at the Electrode

Quantities related to electron density

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Relation of Activity to Surface Electronic Structure

Relation of Large and Small Components in One-Electron Equations

Relation to electron transport

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