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Stabilization mode

Incidentally, isocyanides are polar (for CNC H, the dipole moment is 3.44 D) and they are good bases (vs. BRj, H+), whereas CO is a poor base hence isocyanides can function as ligands in metal complexes where carbon monoxide does not. The scarcity of low-valent isocyanide complexes is less easily explained, however. Arguments involving 77-acceptor capacity are quite inappropriate. More data on low-valent species, and evaluations of stabilities, modes of decomposition, and reactions are desirable. [Pg.24]

Using electrons for the electrolytic reduction of metal salts, Reetz and coworkers have introduced a further variation to the tetraalkylammoniumhalide-stabilization mode [192-198]. The overall electrochemical process can be divided into the following steps (i) oxidative dissolution of the sacrificial Metbuik anode, (ii) migration of Met ions to the cathode, (iii) reductive formation of... [Pg.28]

Alkene hydrogenation is a common field of catalytic application for metal nanoparticles. Various approaches have been utilized to obtain stable and active nanocatalysts in hydrogenation reactions. The main approaches are described in the following sections, and are classified according to the stabilizing mode retained for the nanoparticles. [Pg.220]

The use of dendrimers constitutes an attractive stabilization mode for the synthesis of metal nanoparticles for several reasons ... [Pg.225]

The cartoon-like drawing of the structure of the parent bicylobutonium ion C4H7+ 36 is adopted from an ingenious forward-looking paper of Olah and coworkers in 1972, 61) long before routine 13C-FT-NMR spectroscopy and routine ab initio quantum chemical calculations were available, which envisaged correctly the stabilization mode of the parent bicyclobutonium ion to arise from the interaction of the backside lobe of the Cy-Hendo sp3 orbital with the empty carbenium carbon p-orbital at Ca. [Pg.36]

The performance of the digital temperature controller in the stabilization mode is shown in Fig. 5.10. The ambient temperature was ramped from -10 °C to 90 °C in steps of 10 °C. A reference-temperature digital code of 500 was programmed, which produced a microhotplate temperature of 250 °C. The microhotplate temperature fluctuations owing to ambient temperature variations are less than 2 °C. [Pg.73]

Fig. 5.10. Performance of the digital PID temperatirre controller of the single-ended mixed-signal architecture in the stabilization mode... Fig. 5.10. Performance of the digital PID temperatirre controller of the single-ended mixed-signal architecture in the stabilization mode...
Different types of stabilization modes are known to provide a range of stable carbenes with different electronic and steric properties. In this section, we categorize the stable non-NHC carbenes by the type of stabilization mode involved, in order to highlight their effect on the properties of the carbene as ligand. [Pg.132]

Other substituent, which does not participate in the stabilization, can be considered as a spectator substituent (Scheme 3) [34]. This stabilization system is particularly efficient with an amino group which is not only a 71-donating substituent but also a a-electron withdrawing group. This stabilization mode provides a large choice of substituents allowing an easy functionalization of the corresponding stable mono-aminocarbenes. In fact, several types of acyclic and cyclic amino carbenes have been already synthesized [8, 9]. [Pg.135]

After this brief presentation of stable carbenes with different stabilization modes, we can understand and predict the effect of substituent changes on the carbene properties. In Fig. 1 the HOMO level and S/T energy gap for each family of carbenes are detailed. [Pg.136]

It is clear that the variation in the carbene stabilization modes dramatically modify the carbene properties in terms of steric and electronic factors, which is very essential in the design of new ligands for transition metals. In comparison to classical NHCs, non-NHC carbenes offer a large range of possible structural variations, which should rapidly enhance the interest in non-NHC-based complexes. We can anticipate that the fine tuning of the properties of stable non-NHC carbenes makes these ligands very promising for the development of novel and efficient catalysts. [Pg.145]

The dynamics of the problem can then be understood in terms of the spherical harmonic stability modes consider solutions of the form... [Pg.193]

Thus for a weak imperfection in a system near criticality we see than an imperfection in the presence of a pattern formation mechanism effects the pattern only in regards to its orientation but not its inherent configuration. Indeed the amplitude of the mode is somewhat altered but we notice that the mode itself (in the weak imperfection case) is unchanged, (it is the stability mode that, for example, fixed the ratios of the individual ion currents in the Fucus problems (7.) )... [Pg.209]

The trihalides of aluminum are very strong Lewis acids, and AICI3 finds extensive use as a Friedel-Crafts catalyst as a result of this. A wide variety of adducts are known and these exhibit an enormous range of stability, modes of bonding, structures, and properties. Aromatic hydrocarbons and alkenes only interact weakly but crystalline adducts may be isolated, for example, the clathrate complex AlyBrg CeHg. [Pg.136]

One of the stabilization modes of nitrenes is a coupling to form azo compounds. This dimerization has been observed both in the pyrolysis and the photolysis of aryl azides. The pyrolysis of o-trifluoromethylphenyl azide in the gas phase yielded 80% of bis (o-trifluoromethyl) azobenzene (HI). [Pg.355]

Does the unavailability of adequate valves, piping, etc. limit plant performance and reliability when other modes of operation of the existing plant can be utilized to improve performance (e.g., operate activated sludge plant in plug, step, or contact stabilization mode operate RBCs in step loading mode) ... [Pg.136]

For clarity, the results obtained on noble metals, magnetic metals, and other metals, and main group elements will be reported separately. The chosen examples will allow the presentation of the different stabilization modes that can be used with this method to get well-defined nanoparticles. [Pg.77]


See other pages where Stabilization mode is mentioned: [Pg.28]    [Pg.159]    [Pg.160]    [Pg.228]    [Pg.238]    [Pg.65]    [Pg.364]    [Pg.157]    [Pg.157]    [Pg.369]    [Pg.132]    [Pg.132]    [Pg.623]    [Pg.260]    [Pg.380]    [Pg.351]    [Pg.260]    [Pg.380]    [Pg.132]    [Pg.132]    [Pg.135]    [Pg.60]    [Pg.457]    [Pg.426]    [Pg.350]    [Pg.352]   
See also in sourсe #XX -- [ Pg.73 , Pg.91 ]




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