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Common electronic

The source requited for aes is an electron gun similar to that described above for electron microscopy. The most common electron source is thermionic in nature with a W filament which is heated to cause electrons to overcome its work function. The electron flux in these sources is generally proportional to the square of the temperature. Thermionic electron guns are routinely used, because they ate robust and tehable. An alternative choice of electron gun is the field emission source which uses a large electric field to overcome the work function barrier. Field emission sources ate typically of higher brightness than the thermionic sources, because the electron emission is concentrated to the small area of the field emission tip. Focusing in both of these sources is done by electrostatic lenses. Today s thermionic sources typically produce spot sizes on the order of 0.2—0.5 p.m with beam currents of 10 A at 10 keV. If field emission sources ate used, spot sizes down to ca 10—50 nm can be achieved. [Pg.283]

Donors a.ndAcceptors. Table 3 Hsts common electron—donor groups, and electron—acceptor groups selected from a large number capable of evoking fluorescence. [Pg.295]

Although sp3 hybridization is the most common electronic state of carbon, it s not the only possibility. Look at ethylene, C2H4, for example. It was recognized more than 100 years ago that ethylene carbons can be tetravalent only if they share four electrons and are linked by a double bond. Furthermore, ethylene is planar (flat) and has bond angles of approximately 120° rather than 109.5°. [Pg.15]

While sharing of electrons, i.e., covalent bonding, is the major component of the cohesive force in intermetallics, rationalization of their structure formation based on such chemical bonding is not trivial, because of the failure of the common electron counting rules that chemists have developed over the years from the studies of covalent compounds. The origin of the problem is the well-delo-... [Pg.183]

Fig. 7.7 Schematic diagrams for common electron configurations of Ni " complexes in the one-electron approximation. The resulting valence electron contributions V z are obtained from Table 4.2... Fig. 7.7 Schematic diagrams for common electron configurations of Ni " complexes in the one-electron approximation. The resulting valence electron contributions V z are obtained from Table 4.2...
Links between atoms serve to compensate for the lack of the electrons which are necessary to attain the electron configuration of the next noble gas in the periodic table. With a common electron pair between two atoms each of them gains one electron in its valence shell. As the two electrons link two centers , this is called a two-center two-electron bond or, for short, 2c2e bond. If, for an element, the number of available partner atoms of a different element is not sufficient to fill the valence shell, atoms of the same element combine with each other, as is the case for polyanionic compounds and for the numerous organic compounds. For the majority of polyanionic compounds a sufficient number of electrons is available to satisfy the demand for electrons with the aid of 2c2e bonds. Therefore, the generalized 8 —N rule is usually fulfilled for polyanionic compounds. [Pg.138]

I.I. Electron Bombardment Plasma Sources. These gas-feed sources generally employ Ar or Xe at relatively low vapour pressures (10 3mbar). A heated cathode is a common electron source, and these are accelerated towards an anode to give them... [Pg.73]

All of these trinuclear clusters are 42e and this is the most common electron count. However, a 46e cluster, [Pt3(/r-CO)(/r-dppm)4]2+ has been obtained by reacting [Pt3(/r-dppm)3(PPh3)] with CO.537 The Pt—Pt bond lengths (2.620-2.648 A) are remarkably similar to those in the 42e clusters.537... [Pg.733]

UHV techniques are usually classified in terms of the electron/photon method, as is shown in Table 2.3 which lists the common electron bombardment and emission techniques that have been employed in electrochemical studies. A detailed description of UHV surface analysis techniques is beyond the scope of this book there are many excellent reference texts that can be consulted for this purpose (see further reading list). It is sufficient to note that methods involving electron bombardment or emission are inherently surface-sensitive as a result of the low pathlength, or escape depth, of electrons in condensed media. In addition, Table 2.3 briefly describes the type of information each method provides. [Pg.225]

Benzpinacols (or their trimethylsilyl ethers) are effective electron donors and readily form vividly colored charge-transfer complexes with common electron acceptors such as chloranil (CA), dichlorodicyanobenzoquinone (DDQ), tetracyanobenzene (TCNB), methyl viologen (MV2+), and nitrosonium (NO+) cation.191-194 For example, the exposure of a silylated benzpinacol to chloranil... [Pg.253]

The molecular structure of the parent compound was investigated in the vapor and in the solid phase using X-ray, XN and GED methods. The reported data are shown in Table 16. In both phases a clear bond length separation could be detected with a localized three-membered ring and its three adjacent double bonds. The symmetry-equivalent cyclopropane bonds are rather long in C3v-symmetric BUL (1.533-1.542 A), which can be explained by the common electron-withdrawing effect of the 7r-systems in a. svM-ciinal conformation. For comparison, the unaffected bonds in unsubstituted cyclopropane are 1.499 A in the crystal and 1.510 A in the gas phase. Therefore, the bond lengths in BUL... [Pg.48]

Alvaro, M., Ferrer, B., Fornes, V., Garcia, H. and Scaiano, J.C. (2002). Bipyridinium macroring encapsulated within zeolite Y supercages. Preparation and intrazeolitic photochemistry of a common electron acceptor component of rotaxanes and catenanes. J. Phys. Chem. B 106, 6815-6820... [Pg.263]

For instance, Kochi and co-workers [89,90] reported the photochemical coupling of various stilbenes and chloranil by specific charge-transfer activation of the precursor donor-acceptor complex (EDA) to form rrans-oxetanes selectively. The primary reaction intermediate is the singlet radical ion pair as revealed by time-resolved spectroscopy and thus establishing the electron-transfer pathway for this typical Paterno-Biichi reaction. This radical ion pair either collapses to a 1,4-biradical species or yields the original EDA complex after back-electron transfer. Because the alternative cycloaddition via specific activation of the carbonyl compound yields the same oxetane regioisomers in identical molar ratios, it can be concluded that a common electron-transfer mechanism is applicable (Scheme 53) [89,90]. [Pg.217]

We are faced with locating molecules that are sparse within the environment, hence the term trace. There are several basic steps that are necessary, independent of the design of the specific system or the technology being incorporated. Table 1.1 lists those steps and correlates them with more common electronic instrumentation nomenclature. Some of the actions will involve... [Pg.10]

The detectors used in mass spectrometers for atmospheric applications are essentially the same as for other MS applications and are commonly electron multipliers, either channeltrons or multichannel plate... [Pg.566]

Table 6 contains two other examples of multibranched structures consisting of one, two, or three branches around a common electron-rich tripheny-lamine core. In the first case, oc.6-8, the linear units belong to class III of Fig. 8 and share one of the terminal amine groups [122]. The 2PA spectra of these three compounds, studied by Yoo et al, exhibit a peak at the same wavelength (AmL = 840 nm), while a small red shift was observed in the position of the one-photon absorption band (473, 492, and 495 nm for 0C.6, OC.7, and oc.8, respectively) [122]. The authors also reported an enhancement in the 2PA cross section going from one to three branches, by a factor larger than the increase in the number of branches (the ratio of 5max for 0C.6, OC.7, and oc.8 are 1 2.3 3.7, while the number of branches increases as 1 2 3). [Pg.45]

Common electronic noses are so called as they are often aimed at detection of odorous compounds it is generally not clear that discriminations are based on odorous rather than non-odorous, and possibly incidental, components of the headspace. In the headspace of a food sample, odorants contributing to the flavour may be present in low concentrations, whereas non-odorous molecules can be present in much larger numbers and higher concentration. In such cases. [Pg.334]

Although common electronic noses are generally not suitable for odour assessment, they can be successfully used in applications where the main components in the headspace are directly correlated with the property to be determined (e.g. quality of spice mixtures) or in cases where substances are formed and released into the headspace, for example owing to oxidation processes, fermentation, microbial contamination, thermal treatment, etc. [Pg.336]

D.c. electrical conductivity, thermal conductivity, Seebeck effect and Hall effect are some of the common electron-transport properties of solids that characterize the nature of charge carriers. On the basis of electrical properties, solid materials may be classified into metals, semiconductors, and insulators where the charge carriers move in band states (Fig. 6.1) there are other semiconductors and insulators where charge carriers are localized and their motion involves a diffusive process (Honig, 1981). We shall briefly present the important relations involved in interpreting the transport phenomena in solids. [Pg.302]

Scheme 1 summarizes some of the common electron-impact induced fragmentation pathways available to thietanes, thietes and their 5-oxides. Major processes include retro-2 + 2 fragmentation for thietanes, thiolactones and iminothietanes, loss of sulfur oxides for thietane 5-oxides, and loss of an a-hydrogen atom from thietes and benzothietes. Certain of these processes, considered to involve electron-impact induced pathways, may actually involve thermolytic reactions occurring in the source region of the mass spectrometer (78JHC421,71JA676). [Pg.417]

Nearly all combinations of common electron-excessive heteroaromatics have been achieved by modification of this procedure. However, this procedure has not been successful so far with electron-deficient heteroaromatics (76JOC2536). However, bis-Wittig heterocyclic reagents (75S765) have been condensed with a variety of dialdehydes to generate a series of annulenones (e.g. 47) and annulenes (78HCA2763, for a review see 77CRV513). [Pg.769]

Common electron acceptors that will participate in nitrosating reactions include nitrogen dioxide, transition metals, and possibly oxygen. For example, nitric ox-... [Pg.25]

The most common electron transfer process in organic chemistry, the SRN1 reaction, takes place somewhat differently. This particular reaction [e.g. (90)]... [Pg.156]

The trans influence is another common electronic effect observed in coordination complexes. It is perhaps best known in planar d8 species such as Pt(II) complexes and we have developed an LFMM treatment for a range of ligands (21). Since we use homoleptic complexes as the basis for parameterization and not all species are available experimentally, this study was based exclusively on DFT. [Pg.19]


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See also in sourсe #XX -- [ Pg.99 ]




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