Proton transfer functional groups

Polymer membranes have low proton conductivity until they contain enough proton conductive functional groups, e.g., sulfonic acid, in polymer backbones or side chains. Sulfonic acid in polymer chains shows a high dissociation constant, resulting in high proton conductivity in aqueous environments compared with other acids therefore, most DMFC membranes use the sulfonic moiety as the proton transfer medium. Sulfonation methods of polymer membranes are generally classified as post-sulfonation in the presence of polymers and in situ sulfonation through co-polymerization of sulfonated monomers and nonsulfonated monomers. 

In the El mechanism, the leaving group has completely ionized before C—H bond breaking occurs. The direction of the elimination therefore depends on the structure of the carbocation and the identity of the base involved in the proton transfer that follows C—X heterolysis. Because of the relatively high energy of the carbocation intermediate, quite weak bases can effect proton removal. The solvent m often serve this function. The counterion formed in the ionization step may also act as the proton acceptor ... 

The cyanide ion plays an important role in this reaction, for it has three functions in addition to being a good nucleophile, its electron-withdrawing effect allows for the formation of the carbanion species by proton transfer, and it is a good leaving group. These features make the cyanide ion a specific catalyst for the benzoin condensation. 

For condensation polymerization, it is necessary to have two functional groups on each monomer and to mix stoichiometric amounts of the reactants. In polyamide production, the starting materials first form nylon salt by proton transfer ... 

In molecules with both an acidic and a basic function, there is in principle the possibility of an intramolecular proton transfer leading to betaines (see above). Due to the values of the functional groups, pyridine and carboxylic acid, in [66] no intramolecular proton transfer takes place and no betaine is formed. 

C17-0120. In aqueous solution, amino acids exist as zwitterions (German for double ions ), compounds in which internal proton transfer gives a molecule with two charged functional groups. Use Lewis structures to illustrate the proton transfer equilibrium between the uncharged form of glycine (NH2 CH2 CO2 H) and its zwitterion form. 

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