Amphoteric reactivity

Boron is a hard metalloid with pronounced nonmetallic properties. Aluminum is a light, strong, amphoteric, reactive metallic element with a surface that becomes passivated when exposed to air. 

Aluminum is a light, strong, amphoteric, reactive metallic element... 

Beryllium is readily attacked by most acids and, being amphoteric, is slowly attacked by caustic alkalis with the evolution of hydrogen. As might be anticipated, in view of the controlling influence of the surface film of beryllia on corrosion behaviour, concentrated nitric acid has little effect on beryllium , while the dilute acid results in slow attack. Hot acid is much more reactive. Nitric acid is in fact often used to pickle-off residual mild steel from hot-extruded clad beryllium. 

Zinc and cadmium are both silvery, reactive metals that are similar to each other but differ sharply from mercury. Zinc is amphoteric (like its main-group neighbor aluminum). It reacts with acids to form Zn2+ ions and with alkalis to form the zincate ion, [Zn(OH)4]2 ... 

Ellis Wilson (1991, 1992) examined cement formation between a large number of metal oxides and PVPA solutions. They concluded that setting behaviour was to be explained mainly in terms of basicity and reactivity, noting that cements were formed by reactive basic or amphoteric oxides and not by inert or acidic ones (Table 8.3). Using infrared spectroscopy they found that, with one exception, cement formation was associated with salt formation the phosphonic add band at 990 cm diminished as the phosphonate band at 1060 cm" developed. The anomalous result was that the acidic boric oxide formed a cement which, however, was soluble in water. This was the result, not of an add-base readion, but of complex formation. Infrared spectroscopy showed a shift in the P=0 band from 1160 cm" to 1130 cm", indicative of an interaction of the type... 

Thus we end up with an oxygen atom which is somewhat electron deficient and a carbon atom which is electron rich. The oxygen then would be expected to behave as an electrophilic reagent and the carbon (or rather the regions bounded by the w orbital) should behave as a nucleophilic reagent. The amphoteric nature of the carbonyl n- n singlet state is mirrored in its reactivity toward electron-rich and electron-deficient olefins. 

As mentioned in Table 8.1, amphoteric surfactants contain both an anionic and a cationic group. In acidic media they tend to behave as cationic agents and in alkaline media as anionic agents. Somewhere between these extremes lies what is known as the isoelectric point (not necessarily, or even commonly, at pH 7), at which the anionic and cationic properties are counterbalanced. At this point the molecule is said to be zwitterionic and its surfactant properties and solubility tend to be at their lowest. These products have acquired a degree of importance as auxiliaries in certain ways [20-25], particularly as levelling agents in the application of reactive dyes to wool. 

Amphoteric Wool Acid, metal-complex, reactive, chrome... 

The oils and waxes described as lubricants in section 10.10.1, as well as talc, can be used as softeners but have now been superseded by more effective products. These may be non-reactive or reactive and may be cationic, anionic, nonionic or amphoteric. Although many compounds have been patented, by far the most important are cationic quaternary ammonium compounds and various silicones. Until quite recently the field was led by the cationic types but there is now evidence that aminofunctional polysiloxanes have become the most important product group [482]. 

Amphoteric molecules of this type, where the acidic and basic sites are relatively close to each other but cannot interact directly, can heterolytically cleave H-X and C-X bonds where X is a halide, alkoxide, amide, alcohol, thiol, trimethylsilyl, or alkyl group.18,18a The ability to effect changes in the reactivity of borollide complexes by adjusting metal oxidation states and ligands allows fine-tuning of catalytic and other properties, which in turn advances the application of these compounds in synthesis. 

It is important to establish the origin and magnitude of the acidity (and hence, the charge) of mineral surfaces, because the reactivity of the surface is directly related to its acidity. Several microscopic-mechanistic models have been proposed to describe the acidity of hydroxyl groups on oxide surfaces most describe the surface in terms of amphoteric weak acid groups (14-17), but recently a monoprotic weak acid model for the surface was proposed (U3). The models differ primarily in their description of the EDL and the assumptions used to describe interfacial structure. "Intrinsic" acidity constants that are derived from these models can have substantially different values because of the different assumptions employed in each model for the structure of the EDL (5). Westall (Chapter 4) reviews several different amphoteric models which describe the acidity of oxide surfaces and compares the applicability of these models with the monoprotic weak acid model. The assumptions employed by each of the models to estimate values of thermodynamic constants are critically examined. 

D. Amphoteric Nature, Tendency to Form Adducts, and Reactivity... 

Chlorine monofluoride oxide, 18 328-330 force field of, 18 329, 330 infrared spectrum of, 18 328, 329 stretching force constants for, 18 330 synthesis of, 18 328 Chlorine nitrate fluorination of, 18 332 preparation of, 5 54 Chlorine oxides, 46 109-110, 158 fluorination of, 18 348 Chlorine oxyfluorides, 18 319-389, see also specific compounds adduct formation, 18 327, 328 amphoteric nature of, 18 327, 328 bond lengths, 18 326 bond strengths, 18 323-327 geometry of, 18 320-323 ligand distribution, 18 323 reactivity of, 18 327, 328 stretching force constants, 18 324-327 Chlorine pentafluoride oxide, 18 345, 346 Chlorine trifluoride, reaction with difluoramine, 33 157... 

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