Oxygen electronic structure

The resonance effect of the carbonyl group Electron delocalization expressed by resonance between the following Lewis structures causes the negative charge in acetate to be shared equally by both oxygens Electron delocalization of this type IS not available to ethoxide ion... 

A few free radicals are indefinitely stable. Entries 1, 4, and 6 in Scheme 12.1 are examples. These molecules are just as stable under ordinary conditions of temperature and atmosphere as typical closed-shell molecules. Entry 2 is somewhat less stable to oxygen, although it can exist indefinitely in the absence of oxygen. The structures shown in entries 1, 2, and 4 all permit extensive delocalization of the unpaired electron into aromatic rings. These highly delocalized radicals show no tendency toward dimerization or disproportionation. Radicals that have long lifetimes and are resistant to dimerization or other routes for bimolecular self-annihilation are called stable free radicals. The term inert free radical has been suggested for species such as entry 4, which is unreactive under ordinary conditions and is thermally stable even at 300°C. ... 

Much of the chemistry of oxygen can be rationalized in terms of its electronic structure (2s 2p ), high electronegativity (3.5) and small size. Thus, oxygen shows many similarities to nitrogen (p. 412) in its covalent chemistry, and its propensity to form H bonds (p. 52) and p double bonds (p. 416), though the anionic chemistry of 0 and OH is much more extensive than for the isoelectronic ions N , and NH2. Simi-... 

Examine the geometry of the most stable radical. Is the bonding in the aromatic ring fuUy delocalized (compare to model alpha-tocopherol), or is it localized Also, examine the spin density surface of the most stable radical. Is the unpaired electron localized on the carbon (oxygen) where bond cleavage occurred, or is it delocalized Draw all of the resonance contributors necessary for a full description of the radical s geometry and electronic structure. 

Of course, that is not in fact the case. It would be a mistake, however, to dismiss Thomson s work. He and his contemporaries did not know the number of electrons in any particular atom. Thomson believed, for example, that an oxygen atom had as many as 56 electrons, whereas the current value stands at just eight. Rather, his scheme should be considered an attempt to explain periodicity according to similarities in electronic structures between different elements. 

Moffitt, W., Proc. Roy. Soc. London) A210, 224, The electronic structure of the oxygen molecule. ... 

Kotani, M., Mizuno, Y., Kayama, K., and Ishiguro, E., J. Phys. Soc. Japan 12, 707, Electronic structure of simple diatomic homonuclear molecules. I. Oxygen molecule. ... 

Correa and Waters50 also proposed a mechanistic scheme where the key step of the overall reaction involves the recombination of sulfonyl radicals to form an intermediate with an O—S bond, the decomposition of which yields a sulfinyl radical (ArSO ) and an oxygen-centered radical ArS020 Later this suggestion was further strengthened on the basis of ESR studies51 and thanks to the elucidation of the electronic structure of sulfonyl radicals. However, it seems to the author that the available literature data point to an overall mechanism for equation 17 more complex that the one suggested50 (cf., for... 

As examples we may discuss CO, CN, Nj and NO. CO might be composed of normal or excited atoms, or even of ions. A neutral oxygen atom can form only two bonds. Hence a normal carbon atom, 3P, which can also form two bonds, is at no disadvantage. We can write the following reaction, using symbols similar to those of Lennard-Jones29 and Dunkel,30 whose treatments of the electronic structure of simple molecules have several points of similarity with ours... 

Figure 6.28. Schematic illustration of the change in local electronic structure of an oxygen atom adsorbing on the late transition metal rhodium, the DOS of which is shown on the right-hand side. The interaction of the oxygen 2p orbital with the sp band of the transition metal is illustrated through interaction with the idealized free-electron...

The different classes of Ru-based catalysts, including crystalline Chevrel-phase chalcogenides, nanostructured Ru, and Ru-Se clusters, and also Ru-N chelate compounds (RuNj), have been reviewed recently by Lee and Popov [29] in terms of the activity and selectivity toward the four-electron oxygen reduction to water. The conclusion was drawn that selenium is a critical element controlling the catalytic properties of Ru clusters as it directly modifies the electronic structure of the catalytic reaction center and increases the resistance to electrochemical oxidation of interfacial Ru atoms in acidic environments. 

Stamenkovic V, Mun BS, Mayrhofer KJJ, Ross PN, Markovic NM, Rossmeisl J, Greeley J, Nprskov JK. 2006. Changing the activity of electrocatalysts for oxygen reduction by tuning the surface electronic structure. Angew Chem Int Ed 45 2897. 

PEMFC)/direct methanol fuel cell (DMFC) cathode limit the available sites for reduction of molecular oxygen. Alternatively, at the anode of a PEMFC or DMFC, the oxidation of water is necessary to produce hydroxyl or oxygen species that participate in oxidation of strongly bound carbon monoxide species. Taylor and co-workers [Taylor et ah, 2007b] have recently reported on a systematic study that examined the potential dependence of water redox reactions over a series of different metal electrode surfaces. For comparison purposes, we will start with a brief discussion of electronic structure studies of water activity with consideration of UHV model systems. 

Figure 8.12 Relationships between the catalytic properties and electronic structure of Pt3M alloys correlation between the specific activity for the oxygen reduction reaction measured experimentally by a rotating disk electrode on Pt3M surfaces in 0.1 M HCIO4 at 333 K and 1600 lev/min versus the li-band center position for (a) Pt-skin and (b) Pt-skeleton surfaces. (Reprinted with permission from Stamenkovic et al. [2007b]. Copyright 2007. Nature Pubhshing Group.)...

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