Functional anion concept

ThermodynamicTuning of Single Phase Hydrides by Substitution on the Hydrogen Sites Functional Anion Concept... 

To conclude The functional anion concept opens up ne v possibilities to tailor reaction enthalpies of high capacity hydrides to vards potential applications. At present, ho vever, not much is known about how successful this method will eventually be and which material classes can be successfully altered by it. 

Contrary to the classical approach the recently applied functional anion concept considers the substitution on H-sites by anions. First results indicate that this approach again is very promising for altering reaction enthalpies of complex hydrides. 

Lewis acidic hosts (Section V.A) illustrated important theoretical concepts such as the chelate effect and binding cooperativity, which have now been shown to exist for anion as well as cation binding. This work has also resulted in the crystallographic determination of eye-catching solid state receptor-anion complexes, while heteroelement NMR has allowed an accurate means of probing the solution phase structure of these complexes. Already, multinuclear tin systems are being built into functioning anion selective electrodes. 

In principle, numerous reports have detailed the possibility to modify an enzyme to carry out a different type of reaction than that of its attributed function, and the possibility to modify the cofactor of the enzyme has been well explored [8,10]. Recently, the possibility to directly observe reactions, normally not catalyzed by an enzyme when choosing a modified substrate, has been reported under the concept of catalytic promiscuity [9], a phenomenon that is believed to be involved in the appearance of new enzyme functions during the course of evolution [23]. A recent example of catalytic promiscuity of possible interest for novel biotransformations concerns the discovery that mutation of the nucleophilic serine residue in the active site of Candida antarctica lipase B produces a mutant (SerlOSAla) capable of efficiently catalyzing the Michael addition of acetyl acetone to methyl vinyl ketone [24]. The oxyanion hole is believed to be complex and activate the carbonyl group of the electrophile, while the histidine nucleophile takes care of generating the acetyl acetonate anion by deprotonation of the carbon (Figure 3.5). 

It is assumed that the quantity Cc is not a function of the electrolyte concentration c, and changes only with the charge cr, while Cd depends both on o and on c, according to the diffuse layer theory (see below). The validity of this relationship is a necessary condition for the case where the adsorption of ions in the double layer is purely electrostatic in nature. Experiments have demonstrated that the concept of the electrical double layer without specific adsorption is applicable to a very limited number of systems. Specific adsorption apparently does not occur in LiF, NaF and KF solutions (except at high concentrations, where anomalous phenomena occur). At potentials that are appropriately more negative than Epzc, where adsorption of anions is absent, no specific adsorption occurs for the salts of... 

A concept of anion mobility may be considered a useful paradigm for explaining the net retention and loss of cations from soils, and thus exposure pathways. This paradigm relies on the simple fact that total cations must balance total anions in soil solution (or any other solution), and, therefore, total cation leaching can be thought of as a function of total anion leaching. The net production of anions within the soil (e.g., by oxidation or hydrolysis reactions) must result in the net production of cations (normally H+), whereas the net retention of anions (by either absorption or biological uptake) must result in the net retention of cations. 

Functionalization of these reactive anionic chain ends can be achieved by a variety of methods all based on the general concepts of carbanion chemistry. For example, reaction with C02 or succinnic anhydride leads to the carboxy terminated derivatives [10], while hydroxy-terminated polymers can be easily obtained by reaction with ethylene oxide (Scheme 3) [11]. In select functionalization reactions, such as alkylation with p-vinyl benzyl chloride, the nucleophilicity of the carbanionic species may be necessary and this can be achieved by reaction of the chain end with 1,1-diphenylethene followed by functionalization [12,13]. 

The concept of molecular orbitals (MOs) helps to explain the electron structure of ion-radicals. When one electron abandons the highest occupied molecular orbital (HOMO), a cation radical is formed. HOMO is a bonding orbital. If one electron is introduced externally, it takes the lowest unoccupied molecular orbital (LUMO), and the molecule becomes an anion-radical. LUMO is an antibonding orbital. Depending on the HOMO or LUMO involved in the redox reaction, organic donors appear as n, a, or n species, whereas organic acceptors can be tt or a species. Sometimes, a combination of these functions takes place. 

The concept that the ionic radius is relatively independent of the structure of the solid arose intuitively from experimental observations carried out on alkali halides, which are ionic solids par excellence. Figure 1.3 shows the evolution of interatomic distances in alkali halides as a function of the types of anion and cation, respectively. Significant parallelism within each of the two families of curves may be noted. This parallelism intuitively generates the concept of constancy of the ionic radius. 

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