Carbon valence state

The C—S bond lengths vary upon changing carbon valence states. However, the sulfones and sulfoxides show less sensitivity to these changes than the analogous sulfides . These effects can be illustrated by considering the C—S bond lengths (A) in analogous dimethyl and diphenyl derivatives ... 

Figure 8. S-C and Se-C bond lengths in sulfides and selenides with various carbon valence states (after [48]).

Methane, CH4. The hydrogen atoms are at the corners of a regular tetrahedron, with the carbon at the centre. A carbon valence state with four identical, singly occupied hybrid AO s can be set up by allowing the mixing of 2s and all the 2p AO s. When they arc denoted by h, hg, hg, and h4, the carbon valence state is C(ls2 h hg hg h4 ). The... 

All known valence states of carbon are laid down on the graph of all 139 valence states of atoms. The quadruplets of valence states 1 >,V3,V4 (Sect. 4.3), denoted here as N, S, D, T, respectively, are encircled. The numbers of lone electrons (N) on the top two lines are propagated vertically down for all vectors, the triplets (SDT) on the left are propagated horizontally. Carbon valence states intercon-vertable by elementary conversions are Joined by heavy lines. For example, the vertex (2200), which lies in the line beginning with description (200) under the circle for N=2, represents the carbon in... 

Values of the coefficients a, b and c were derived for common elements in their usual valence. states (for example, for carbon there are different values for sp, sp Tr and spw valence states). 

The relative toxicities of thallium compounds depend on their solubHities and valence states. Soluble univalent thallium compounds, eg, thaHous sulfate, acetate, and carbonate, are especiaHy toxic. They are rapidly and completely absorbed from the gastrointestinal tract, skin peritoneal cavity, and sites of subcutaneous and intramuscular injection. Tb allium is also rapidly absorbed from the mucous membranes of the respiratory tract, mouth, and lungs foHowing inhalation of soluble thallium salts. Insoluble compounds, eg, thaHous sulfide and iodide, are poorly absorbed by any route and are less toxic. 

Under polymerisation conditions, the active center of the transition-metal haHde is reduced to a lower valence state, ultimately to which is unable to polymerise monomers other than ethylene. The ratio /V +, in particular, under reactor conditions is the determining factor for catalyst activity to produce EPM and EPDM species. This ratio /V + can be upgraded by adding to the reaction mixture a promoter, which causes oxidation of to Examples of promoters in the eadier Hterature were carbon tetrachloride, hexachlorocyclopentadiene, trichloroacetic ester, and hensotrichloride (8). Later, butyl perchlorocrotonate and other proprietary compounds were introduced (9,10). 

A second doping method is the substitution of an impurity atom with a different valence state for a carbon atom on the surface of a fullerene molecule. Because of the small carbon-carbon distance in fullerenes (1.44A), the only species that can be expected to substitute for a carbon atom in the cage is boron. There has also been some discussion of the possibility of nitrogen doping, which might be facilitated by the curvature of the fullerene shell. However, substitutional doping has not been widely used in practice [21]. 

We would normally write the electronic ground state electron configuration of a carbon atom as ls-2s 2p-. Despite the intellectual activity that has gone into defining mythical valence states for carbon atoms in different bonding situations, no one would include a d-orbital in the description of ground state carbon. 

Other treatments " have led to scales that are based on different principles, for example, the average of the ionization potential and the electron affinity, " the average one-electron energy of valence shell electrons in ground-state free atoms, or the compactness of an atom s electron cloud.In some of these treatments electronegativities can be calculated for different valence states, for different hybridizations (e.g., sp carbon atoms are more electronegative than sp, which are still more electronegative than and even differently for primary, secondary,... 

For example, the ir-eiectron energy change in the dimerization of benzyl is taken as a twofold difference in the rr-electron energies of benzene and benzyl. With the SCF data, a double value of the valence state ionization potential of carbon [I in eq. (25)] has to be added to this difference. The entries of Table XII show that in all equilibria considered, a dimer is favored. 

W results not only from their redox-active ranging through oxidation states VI-IV, but because the intermediate V valence state is also accessible, they can act as interfaces between one- and two-electron redox systems, which allows them to catalyse hydroxylation of carbon atoms using water as the ultimate source of oxygen, (Figure 17.1) rather than molecular oxygen, as in the flavin-, haem- or Cu-dependent oxygenases, some of which we have encountered previously. For reviews see Hille, 2002 Brondino et al., 2006 Mendel and Bittner, 2006. 

Walsh, A. D. Discussions Faraday Soc. 2, 18 (1947) Walsh stated the following rule if a group X attached to carbon is replaced by a more electronegative gTOup Y, the carbon valency toward Y has more p character than it had toward X. For a review, see Bent, H. A. Chem. Revs. 61, 275 (1961)... 

Electronic ligand effects are highly predictable in oxidative addition reactions a-donors strongly promote the formation of high-valence states and thus oxidative additions, e.g. alkylphosphines. Likewise, complexation of halides to palladium(O) increases the electron density and facilitates oxidative addition [11], Phosphites and carbon monoxide, on the other hand, reduce the electron density on the metal and thus the oxidative addition is slower or may not occur at all, because the equilibrium shifts from the high to the low oxidation state. In section 2.5 more details will be disclosed. 

When two electrons are transferred from a phenoxide anion to the copper dimer, we form the phenoxonium cation and two copper(I) ions are formed. Most likely, the phenoxonium cations are not free in solution, but they are still coordinated to copper. The valence state cannot be rapidly deducted from the picture and thus we have indicated that below the respective complexes. A nucleophilic attack by another phenol (or phenoxide anion) takes place at carbon-4 of the phenoxonium ion (Figure 15.17). 

Figure 7.9 Light-dependent binding of CO to Ni at the level of the Ni -C state. After mixing of H2-reduced enzyme with CO-saturated buffer in the dark, the Nij-C state is formed within 10 ms. Carbon monoxide does not bind to Ni due to its high valence state. When illuminated at 30 K the Ni -L state is formed, where the charge density at the Ni-Fe site has greatly increased (see also the shift of the FTIR bands in Fig. 7.6). Upon raising the temperature to 200 K in the dark, the nearby CO now can bind to the electron-rich Ni.The Ni. CO species has been earlier characterized by our group.

An interesting deoxygenation of ketones takes place on treatment with low valence state titanium. Reagents prepared by treatment of titanium trichloride in tetrahydrofuran with lithium aluminum hydride [205], with potassium [206], with magnesium [207], or in dimethoxyethane with lithium [206] or zinc-copper couple [206,209] convert ketones to alkenes formed by coupling of the ketone carbon skeleton at the carbonyl carbon. Diisopropyl ketone thus gave tetraisopropylethylene (yield 37%) [206], and cyclic and aromatic ketones afforded much better yields of symmetrical or mixed coupled products [206,207,209]. The formation of the alkene may be preceded by pinacol coupling. In some cases a pinacol was actually isolated and reduced by low valence state titanium to the alkene [206] (p. 118). 

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