Bronsted formation

Raman spectroscopy has provided information on catalytically active transition metal oxide species (e. g. V, Nb, Cr, Mo, W, and Re) present on the surface of different oxide supports (e.g. alumina, titania, zirconia, niobia, and silica). The structures of the surface metal oxide species were reflected in the terminal M=0 and bridging M-O-M vibrations. The location of the surface metal oxide species on the oxide supports was determined by monitoring the specific surface hydroxyls of the support that were being titrated. The surface coverage of the metal oxide species on the oxide supports could be quantitatively obtained, because at monolayer coverage all the reactive surface hydroxyls were titrated and additional metal oxide resulted in the formation of crystalline metal oxide particles. The nature of surface Lewis and Bronsted acid sites in supported metal oxide catalysts has been determined by adsorbing probe mole-... 

Metal ion complexation rates have been studied by the T-jump method. ° Divalent nickel and cobalt have coordination numbers of 6, so they can form complexes ML with monodentate ligands L with n = 1—6 or with bidentate ligands, n = 1-3. The ligands are Bronsted bases, and only the conjugate base form undergoes coordination with the metal ion. The complex formation reaction is then... 

Friedel-Crafts reactions have been studied in detail by Olah [74, 75]. These reactions result in the formation of carbon-carbon bonds and are catalyzed by strong Bronsted or Lewis acids. 

Acid-treated clays were the first catalysts used in catalytic cracking processes, but have been replaced by synthetic amorphous silica-alumina, which is more active and stable. Incorporating zeolites (crystalline alumina-silica) with the silica/alumina catalyst improves selectivity towards aromatics. These catalysts have both Fewis and Bronsted acid sites that promote carbonium ion formation. An important structural feature of zeolites is the presence of holes in the crystal lattice, which are formed by the silica-alumina tetrahedra. Each tetrahedron is made of four oxygen anions with either an aluminum or a silicon cation in the center. Each oxygen anion with a -2 oxidation state is shared between either two silicon, two aluminum, or an aluminum and a silicon cation. 

A proton (H+) is an electron pair acceptor. It is therefore a Lewis acid because it can attach to ( accept") a lone pair of electrons on a Lewis base. In other words, a Bronsted acid is a supplier of one particular Lewis acid, a proton. The Lewis theory is more general than the Bronsted-Lowry theory. For instance, metal atoms and ions can act as Lewis acids, as in the formation of Ni(CO)4 from nickel atoms (the Lewis acid) and carbon monoxide (the Lewis base), but they are not Bronsted acids. Likewise, a Bronsted base is a special kind of Lewis base, one that can use a lone pair of electrons to form a coordinate covalent bond to a proton. For instance, an oxide ion is a Lewis base. It forms a coordinate covalent bond to a proton, a Lewis acid, by supplying both the electrons for the bond ... 

Mond process The purification of nickel by the formation and decomposition of nickel carbonyl, monomer A small molecule from which a polymer is formed. Examples CH2=CH2 for polyethylene NH2(CH2)6NH2 for nylon, monoprotic acid A Bronsted acid with one acidic hydrogen atom. Example CH COOI I. monosaccharide An individual unit from which carbohydrates are considered to be composed. Example C6H(206, glucose, multiple bond A double or triple bond between two atoms. 

The thermal decompositions are catalyzed by Bronsted and Lewis acids [68]. In general, when M is electron poor and Lewis acidic, the thermal decompositions occur efficiently and at low temperatures (typically between 100 and 200 °C, but sometimes at lower temperature). The addition of a catalytic amount of a Lewis or Bronsted acid (i.e., AICI3 or HCl) has been observed to accelerate the ehmination of isobutylene and the formation of three-dimensional network structures [64,124-126]. Pioneering studies on pyrolyses of various metal alkoxides by Bradley and others have also shown that alkene eliminations represent a primary decomposition pathway [104]. 

This concept covers most situations in the theory of AB cements. Cements based on aqueous solutions of phosphoric acid and poly(acrylic acid), and non-aqueous cements based on eugenol, alike fall within this definition. However, the theory does not, unfortunately, recognize salt formation as a criterion of an acid-base reaction, and the matrices of AB cements are conveniently described as salts. It is also uncertain whether it covers the metal oxide/metal halide or sulphate cements. Bare cations are not recognized as acids in the Bronsted-Lowry theory, but hydrated... 

Although Lewis and Bronsted bases comprise the same species, the same is not true of their acids. Lewis acids include bare metal cations, while Bronsted-Lowry acids do not. Also, Bell (1973) and Day Selbin (1969) have pointed out that Bronsted or protonic acids fit awkwardly into the Lewis definition. Protonic acids cannot accept an electron pair as is required in the Lewis definition, and a typical Lewis protonic add appears to be an adduct between a base and the add (Luder, 1940 Kolthoff, 1944). Thus, a protonic acid can only be regarded as a Lewis add in the sense that its reaction with a base involves the transient formation of an unstable hydrogen bond adduct. For this reason, advocates of the Lewis theory have sometimes termed protonic adds secondary acids (Bell, 1973). This is an unfortunate term for the traditional adds. 

Spectroscopy. In the methods discussed so far, the information obtained is essentially limited to the analysis of mass balances. In that re.spect they are blind methods, since they only yield macroscopic averaged information. It is also possible to study the spectrum of a suitable probe molecule adsorbed on a catalyst surface and to derive information on the type and nature of the surface sites from it. A good illustration is that of pyridine adsorbed on a zeolite containing both Lewis (L) and Brbnsted (B) acid sites. Figure 3.53 shows a typical IR ab.sorption spectrum of adsorbed pyridine. The spectrum exhibits four bands that can be assigned to adsorbed pyridine and pyridinium ions. Pyridine adsorbed on a Bronsted site forms a (protonated) pyridium ion whereas adsorption on a Lewis site only leads to the formation of a co-ordination complex. 

The formation of telomers rests on Tjhallylic intermediates, and the ratio of formation of 1 1 vs. 1 2 telomers stems from the reaction of the amine on a C4-allylic complex vs. a Cg-allyhc complex, an excess of phosphine and the presence of an acidic (Bronsted or Lewis) co-catalyst favoring the qhcrotyl complex (Scheme 4-5) [178, 180, 189-196]. 

It was G. N. Lewis who extended the definitions of acids and bases still further, the underlying concept being derived from the electronic theory of valence. It provided a much broader definition of acids and bases than that provided by the Lowry-Bronsted concept, as it furnished explanations not in terms of ionic reactions but in terms of bond formation. According to this theory, an acid is any species that is capable of accepting a pair of electrons to establish a coordinate bond, whilst a base is any species capable of donating a pair of electrons to form such a coordinate bond. A Lewis acid is an electron pair acceptor, while a Lewis base is an electron pair donor. These definitions of acids and bases fit the Lowry-Bronsted and Arrhenius theories, and cover many other substances which could not be classified as acids or bases in terms of proton transfer. 

Chiral Bronsted acid co-catalysts do not promote formation of optically enriched products in analogous couplings to pyruvates, although increased rate and conversion in response to the Bronsted acid co-catalyst is unmistakably apparent. For pyruvates, protonation likely occurs subsequent to the C-C... 

In the case of the rhenium aqua-ion [Re(OH2)3(CO)3]+ (33b) the question has been posed whether complex-anion can be considered to be a Bronsted acid. Titrations with hydroxide in water yielded a pKa value of 7.55 which is exceptionally low for a +1 cation. After the deprotonation of one coordinated water molecule, polymer formation over (/r-OH) bridges was initiated and the two compounds [Re3(/T3-OH)(/T-OH)3(CO)9r (35) and [Re2(/i-OH)3(CO)6] were (36) isolated and structurally characterized (Scheme 6). 

Proton electroreduction catalyzed by metal complexes is different from reduction at a metal electrode. It definitely involves the formation of metal hydride species through protonation of electroreduced, low-oxidation-state metal complexes that function as Bronsted base (Equation (5)). From protonated... 

It is worth noting that the partide sizes of samples prepared by the urea hydrolysis method are larger than other LDHs. Such a finding can be rationalized by considering the slow hydrolysis of urea [61], since it can be classified as a very weak Bronsted base (pfCb= 13.8). Its hydrolysis mechanism consists of the formation of ammonium cyanate as the rate-determining step, followed by fast hydrolysis of the cyanate to ammonium carbonate ... 

Recrystallization procedure applied to the amorphous aluminosilicates of different chemical composition resulted in the formation of the dispersed zeolitic domains of the FAU and BEA structure in porous matrices. The structural transformation into the composite material was proved with TEM, XRD and 27Al and 29Si MAS NMR spectroscopies. The IR data revealed that strong Bronsted acid centers were main active sites generated in the composite materials, irrespectively of the Al content. 

The formation of heavy carbonaceous compounds in 5A calcium exchanged zeolites depends on the calcium content. These zeolites are able to protonated ammonia molecules in ammonium ions. This Bronsted acidity results from the presence of CaOH+ species which are formed by water dissociation on Ca2+ ions and have an IR signature at 3515 cm"1. 

The tetrahedral Al incorporated in mesoporous silica reduces considerably the quantity of amorphous carbon, increasing the MWCNTs selectivity, due to the formation of strong Bronsted acidic sites, which allow a better dispersion of iron metallic clusters. The Fe/Al-MCM41 (10) showed the best results in CNT purity and yield. This indicates that the aluminum content and its tetrahedral structural incorporation play an important role in the CNT syntheses. 

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