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Molecules, electron attachment

Electron attachment. A resonance process whereby an electron is incorporated into an atomic or molecular orbital of an atom or molecule. [Pg.438]

Here symbols in parentheses represent unshared electrons attached to C and O, respectively, and those in braces represent shared electrons. An excited carbon atom 6S lies about 1.6 v. e. above the normal state, but can still form only a double bond with oxygen, so that the resultant molecule should be excited. We write... [Pg.82]

These arise either by an analogous process to that described above for Cl, i.e. the adduction of a negatively charged species such as Cl , and the abstraction of a proton to generate an (M — H) ion, or by electron attachment to generate an M ion. The ions observed in the mass spectrum are dependent on the species generated by the reagent gas and the relative reactivities of these with each other and with the analyte molecule. [Pg.56]

Other sensor applications can be considered if some sensitive biological molecules (such as antibodies or receptors) are attached to the nanogranule. If, for example, an antibody molecule is attached to it, then the granule is placed between two electrodes, and single-electron current flows between them. The step value of the coulomb staircase depends on the capacity of the junctions. When the antibody molecule binds specific antigen, the capacity value will be changed, and, therefore, the step value of the VH characteristics will also change. [Pg.185]

There is more than one possibility they are nonstoichiometric but must be electrically neutral. clO-0142. Imagine making an O4 molecule by attaching an oxygen atom to the nonbonding pair of electrons on... [Pg.746]

Much of what is knotm about the structure response of the ECD is based on empirical observations. Clearly, the ability to correlate the response of the detector to fundamental molecular parameters would be useful. Chen and Wentworth have shorn that the information required for this purpose is the electron affinity of the molecule, the rate constant for the electron attachment reaction and its activation energy, and the rate constant for the, ionic recombination reaction [117,141,142]. in general, the direct calculation of detector response factors have rarely Jseen carried j out, since the electron affinities and rate constants for most compounds of interest are unknown. [Pg.144]

The benzene molecule is attached as a phenyl group, between two metal centers (structure I), and as a "benzene four-electron donor, three-center coordinating group in structures II, VI, and X. The C-C distance in all these molecules is 1.42 A, and the dihedral angle between the planes containing the osmium atoms and the mean plane of the benzyne in the three complexes is remarkably constant at 69 3°. [Pg.302]

Anion solvation in alcohol clusters has been studied extensively (see Refs. 135 and 136 and references cited therein). Among the anions that can be solvated by alcohols, the free electron is certainly the most exotic one. It can be attached to neutral alcohol clusters [137], or a sodium atom picked up by the cluster may dissociate into a sodium cation and a more or less solvated electron [48]. Solvation of the electron by alcohols may help in understanding the classical solvent ammonia and the more related and reactive solvent water [138], By studying molecules with amine and alcohol functionalities [139] one may hope to unravel the essential differences between O- and N-solvents. One should note that dissociative electron attachment processes become more facile with an increasing number of O—H groups in the molecule [140],... [Pg.18]

The electron affinity (EA) for a molecule is a quantity which is analogous to the ionization energy for cations. Thus, the electron affinity is defined as the negative of the enthalphy change for the electron attachment reaction ... [Pg.256]

CNTs can conjugate with nucleic acids via non-covalent bond. ssDNA, short double-stranded DNA and total RNA molecules can attach to the surface of CNTs and can disperse CNTs in aqueous environment. The poly(30T) has the highest dispersion efficiency (Zheng et al., 2003). For example, 1 mg DNA molecules mix with lmg CNTs in 1ml water, yield at most 4mg/ml CNT solution. DNA-CNT complexes can be purified or isolated by electronic properties such as agarose gel electrophoresis and centrifuge method (Cui et al., 2004a Karajanagi et al., 2004). [Pg.183]

Figure 6 illustrates the different forms of chemisorption for a C02 molecule. In the weak form of chemisorption the CO2 molecule is attached to the surface by two valence bonds, as depicted in Fig. 6a. This is an example of adsorption on a virtual Mott exciton, that is, not on a pre-prepared Mott exciton which, as already observed, represents a pair of free valencies of opposite sign (electron -j- hole) wandering through the crystal as an entity, but on an exciton produced in the very act of adsorption. As appears from Fig. 6a, this is the valence-saturated and electrically neutral... Figure 6 illustrates the different forms of chemisorption for a C02 molecule. In the weak form of chemisorption the CO2 molecule is attached to the surface by two valence bonds, as depicted in Fig. 6a. This is an example of adsorption on a virtual Mott exciton, that is, not on a pre-prepared Mott exciton which, as already observed, represents a pair of free valencies of opposite sign (electron -j- hole) wandering through the crystal as an entity, but on an exciton produced in the very act of adsorption. As appears from Fig. 6a, this is the valence-saturated and electrically neutral...
The most powerful reducing agent is the solvated electron with a reduction potential of-3.05 V vs. see [60], The LUMO of ethene is too high in energy to permit electron attachment to this molecule but introduction of an electron withdrawing substituent such as carbonyl or nitrile lowers the energy of the LUMO sufficiently that the rate of electron attachment becomes close to diffusion control [61]. Benzene reacts with solvated electrons more slowly than the diffusion controlled limit... [Pg.22]

For collisions involving fast electrons, most of the relevant reactions given by Eqs. (9.1)-(9.13) occur with the primary and secondary electrons leaving the target molecule promptly, in about 10 sec. One the other hand, autoionization and dissociative ionization channels can result in a secondary electron being delayed relative to the primary, and in the case of resonant electron attachment, there may be a measurable delay in the exit of the primary electron. These processes are described in considerable detail by Mark et al. [19]. [Pg.41]


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