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Penning effect

If the work function is smaller than the ionization potential of metastable state (see. Fig. 5.18b), then the process of resonance ionization becomes impossible and the major way of de-excitation is a direct Auger-deactivation process similar to the Penning Effect ionization a valence electron of metal moves to an unoccupied orbital of the atom ground state, and the excited electron from a higher orbital of the atom is ejected into the gaseous phase. The energy spectrum of secondary electrons is characterized by a marked maximum corresponding to the... [Pg.320]

PENNING EFFECT. An increase in the effective ionization rate of a gas due to the presence of a small number of foreign metastable atoms. For instance, a neon atom has a metastable level at 16.6 volts and if there are a few neon atoms in a gas of argon which has an ionization potential of 15.7 volts, a collision between the neon metastable atom with an argon atom may lead to ionization of the argon. Thus, the energy which is stored in the metastable atom can be used to increase the ionization rate. Other gases where this effect is used are helium, with a metastable level at 19.8 volts, and mercury, with an ionization level at 10.4 volts. [Pg.1221]

In accord with the Felkin-Anh model, a-chiral ketones react more diastereoselectively than the corresponding aldehydes. Increasing steric demand of the acyl substituent increases the Cram selectivity. Due to the size of the acyl substituent, the incoming nucleophile is pushed towards the stereogenic center and therefore the diastereoface selection becomes more effective (see also Section 1.3.1.1.). Thus, addition of methyllithium to 4-methyl-4-phenyl-3-hexanonc (15) proceeds with higher diastercoselectivity than the addition of ethyllithium to 3-methyl-3-phenyl-2-pen-tanone (14)32. [Pg.31]

A useful synthesis of allylstannanes from primary alcohols involves conversion of the alcohols into their O-substituted 5-methyl carbonodithioates, thermolysis to effect [3,3] rearrangement to the corresponding 5-substituted 5-methyl carbonodithioates, and treatment with a trialkyl-tin hydride under free-radical conditions to form the allylstannane21. This procedure has been applied to the synthesis of functionalized allylstannanes including (5)-( )-4-(benzyloxy)-2-pen-tenyl(tributyl)stannane22. [Pg.360]

Adequate blood levels of the drug must be maintained for die agent to be effective. Accidental omission or delay of a dose results in decreased blood levels, which will reduce the effectiveness of the antibiotic. It is best to give oral penicillins on an empty stomach, 1 hour before or 2 hours after a meal. Bacampicillin (Spectrobid), penicillin V (Pen-Vee K), and amoxicillin (Amoxil) may be given without regard to meals. [Pg.72]

Recent Uses of Solid-Surface Luminescence Analysis in Environmental Analysis. Vo-Dinh and coworkers have shown very effectively how solid-surface luminescence techniques can be used for environmentally important samples (17-22). RTF has been used for the screening of ambient air particulate samples (17,18). In addition, RTF has been employed in conjunction with a ranking index to characterize polynuclear aromatic pollutants in environmental samples (19). A unique application of RTF reported recently is a personal dosimeter badge based on molecular diffusion and direct detection by RTF of polynuclear aromatic pollutants (20). The dosimeter is a pen-size device that does not require sample extraction prior to analysis. [Pg.157]

Koeman, J.H. and Pennings, J.H. (1970). An orientational survey on the side effects and environmental distribution of dieldrin in a tse-tse control in S.W. Kenya. Bulletin of Environmental Contamination and Toxicology 5, 164—170. [Pg.356]

Apart from the use and need as fragrances, the resins are marketed for medicinal use as antiarthritic and antiinflammatory pharmaceutical products. The pharmacological effects are mainly attributed to the presence of the nonvolatile pen-tacyclic triterpenoid boswellic acids. This class of ingredients is not present in the actual valuable B. frereana species hence, B. frereana plays no part in the pharmaceutical area. [Pg.392]


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See also in sourсe #XX -- [ Pg.1221 ]

See also in sourсe #XX -- [ Pg.220 ]

See also in sourсe #XX -- [ Pg.220 ]

See also in sourсe #XX -- [ Pg.696 ]

See also in sourсe #XX -- [ Pg.236 ]




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Penning

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