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Hydrogen stabilization

The smallest amcAwo-borane is apparently B2H7 13, 35, 58) with a 4"4"- or a 5"5 -bridge hydrogen, stabilized by the presence of the negative charge. [Pg.117]

Johnson and coworkers (Johnson etal., 1986a) found that shallow donor dopants in n-type single-crystal silicon could also be neutralized by hydrogenation, although not as effectively as with boron, Further investigations led Johnson and coworkers (Johnson et al., 1987) to discover the surprising result that H can insert itself between Si—Si bonds to form extended structural defects that may be described as hydrogen-stabilized platelets. [Pg.3]

Infrared spectra of a series of coals and tars demonstrate the very close similarity of tars to their parent coals, providing further evidence that the tar consists of hydrogen-stabilized monomers derived from decomposition of the coal polymer. [Pg.111]

Hitherto we have discussed the formation of amorphous covalent ceramics only on the basis of polymer derived materials. In Sects. 2.2 and 4.2.2.2, thin amorphous, hydrogen stabilized SiC layers (a-SiC H) are also considered which are formed, first of all, by gas phase processes (CVD, PVD). They represent another type of amorphous covalent ceramics. And though it is not expected that properties of such layers agree completely with those of the polymer derived ACC, the basic ideas of stability and transformability of the ACC state discussed above should be transferable to this type of amorphous covalent ceramics, too. [Pg.95]

The augmentation of the basis sets with jxjlarization functions has the same effect in the correlated calculations as they do in the restricted matrix Hartree-Fock calculations, i.e. basis sets with d-polarization functions added to the heavy atoms show a greater energetic stabilization for the syn-conformer and further augmentation with p-polarization functions added to the hydrogens stabilizes the syn -conformer even further. The only exception... [Pg.102]

As mentioned in the mechanistic section, TAD, 02, and RNO reactions have been shown to be special enophiles. Reactions using these enophiles have been well studied and characterized. For example, 02 manifests a cw-effect, which is characterized by H-abstraction from the more substituted side of the alkene, forming a 1 1 mixture of 86 and 87. Furthermore, the hydrogen removed displays a preference for removal from the lone carbon as shown in structure 88. ° Most of the explanations for the transition state are consistent with the idea that the two allylic hydrogens stabilize the transition state. [Pg.15]

Fig 3 Eh-pH diagram of U-O2-H2O-CO2 system at 25°C and 1 atm for U = 10 m and Pcoi = 10" atm. Modified from Langmuir. Upper and lower boundaries within diagram (dotted lines) are limits within which water itself is chemically stable. Above upper limit water is oxidized to give oxygen and below lower limit reduced to yield hydrogen. Stability field for crystalline uraninite shaded predominant U species in solution indicated in various unshaded areas unbroken lines represent equilibrium conditions... [Pg.21]

Catalytic Hydrogenation Stability of Double Bonds CHAPTER 11 1 447... [Pg.447]


See other pages where Hydrogen stabilization is mentioned: [Pg.264]    [Pg.139]    [Pg.18]    [Pg.129]    [Pg.214]    [Pg.356]    [Pg.304]    [Pg.139]    [Pg.336]    [Pg.358]    [Pg.50]    [Pg.214]    [Pg.114]    [Pg.771]    [Pg.304]    [Pg.107]    [Pg.264]    [Pg.224]    [Pg.169]    [Pg.345]    [Pg.210]    [Pg.148]    [Pg.137]    [Pg.1004]    [Pg.148]    [Pg.287]    [Pg.520]    [Pg.166]    [Pg.50]    [Pg.6]    [Pg.175]    [Pg.449]    [Pg.166]   
See also in sourсe #XX -- [ Pg.255 , Pg.256 ]

See also in sourсe #XX -- [ Pg.474 ]




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Hydrogen stability

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