Chemical reactions amide formation

Figure 1.18. A simple chemical reaction (amide formation) and examples of scaffold/R-group combinations...

Each functional group of an amino acid exhibits all of its characteristic chemical reactions. For carboxylic acid groups, these reactions include the formation of esters, amides, and acid anhydrides for amino groups, acylation, amidation, and esterification and for —OH and —SH groups, oxidation and esterification. The most important reaction of amino acids is the formation of a peptide bond (shaded blue). 

Enthalpies are often used to describe the energetics of bond formations. For example, when an amide forms through the condensation reaction between an ester and an amine, the new C-N bond, has an enthalpy of formation of -293 kj/mole. The higher the negative value for the bond enthalpy of formation, the stronger the bond. An even more useful concept is the enthalpy of a reaction. For any reaction, we can use the fact that enthalpy is a state function. A state function is one whose value is independent of the path traveled. So, no matter how we approach a chemical reaction, the enthalpy of the reaction is always the same. The enthalpy of... 

Among the different chemical reactions usable to synthesize polymeric materials by step polymerisation are esterification, amidation, nucleophilic aromatic substitution and urethane (carbamate) formation. Polymerisation... 

Since then, catalytic antibodies which catalyze different chemical reactions have been described. The reactions range from ester or carbonate hydrolysis to carbon-carbon bond forming reactions, bimolecular amide formation or peptide bond cleavage, so the application of catalytic antibodies to general synthetic organic chemistry seems to be very promising [22]. 

Many of the common condensation polymers are listed in Table 1-1. In all instances the polymerization reactions shown are those proceeding by the step polymerization mechanism. This chapter will consider the characteristics of step polymerization in detail. The synthesis of condensation polymers by ring-opening polymerization will be subsequently treated in Chap. 7. A number of different chemical reactions may be used to synthesize polymeric materials by step polymerization. These include esterification, amidation, the formation of urethanes, aromatic substitution, and others. Polymerization usually proceeds by the reactions between two different functional groups, for example, hydroxyl and carboxyl groups, or isocyanate and hydroxyl groups. 

The reaction of acrylamide copolymers and taurine was studied at temperatures between 125° and 200° C, reaction time 2-7 hours, and taurine charge 10-100 mol% based on polymer. The substituted amide formation was determined by NMR and colloid titration. The C-13 NMR of the product exhibits carbonyls consistent with the formation of a secondary amide. The spectrum also exhibits two new methylene signals for the incorporated taurine at chemical shifts slightly different from the starting taurine. Additionally, the chemical shifts for the signals of taurine are pH dependent, whereas little change in chemical shift is observed for the signals of the incorporated taurine. The presence of sulfonate incorporated into the polymer was detected and quantitatively determined by colloid titration at pH 2.5. 

The molecular structure of epoxy/metal interphases in the presence of an amino coupling agent was studied by Boerio and co-workers [28] by IR and by XPS. The formation of amide and imide groups in the interphase provided evidence of chemical reaction between the silane primer and the curing agent for epoxy resin. 

By simulating evolution in vitro it has become possible to isolate artificial ribozymes from synthetic combinatorial RNA libraries [1, 2]. This approach has great potential for many reasons. First, this strategy enables generation of catalysts that accelerate a variety of chemical reactions, e.g. amide bond formation, N-glycosidic bond formation, or Michael reactions. This combinatorial approach is a powerful tool for catalysis research, because neither prior knowledge of structural prerequisites or reaction mechanisms nor laborious trial-and-error syntheses are necessary (also for non-enzymatic reactions, as discussed in Chapter 5.4). The iterative procedure of in-vitro selection enables handling of up to 1016 different compounds... 

Calcium and the other metals are soft and silvery, resembling sodium in their chemical reactivities, although somewhat less reactive. These metals are also soluble, though less readily and to a lesser extent than sodium, in liquid ammonia, giving blue solutions similar to those of the Group 1 metals. These blue solutions are also susceptible to decomposition (with the formation of the amides) and have other chemical reactions similar to those of the Group 1 metal solutions. They differ, however, in that moderately stable metal ammines such as Ca(NH3) + can be isolated on removal of solvent at the boiling point. 

All technical processes for the synthesis of hydrazine yield either hydrazine in aqueous solution or hydrazine hydrate. Most applications can use hydrazine hydrate, but for some applications, for example, rocket propulsion, anhydrous hydrazine is necessary. The water can be removed by a chemical reaction followed by distillation or by azeotropic distillation with an auxiliary fluid. As water binding chemicals, calcium carbide, sodium hydroxide, calcium oxide, calcium hydride, barium oxide, barium hydroxide, and barium pemitride Ba3N4 have been used. The use of sodium or calcium metal and sodium amide is best avoided because of the formation of explosive hydrazides. Starting from hydrazine hydrate (64% hydrazine), sodium hydroxide is generally used... 

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