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Polymers of different architectures will self-assemble into different structures. This self-assembly can occur due to the nature of the polymer and the solvent, or due to a change in pH. pH changes can also cause the larger structure to swell or deswell. For example, block copolymers often form micelles, as will star polymers and branched polymers.
In polymer chemistry, cationic polymerization is a type of chain growth polymerization in which a cationic initiator transfers charge to a monomer, which then becomes reactive. This reactive monomer goes on to react similarly with other monomers to form a polymer .
Living cationic polymerization is a living polymerization technique involving cationic propagating species. [1] [2] It enables the synthesis of very well defined polymers (low molar mass distribution) and of polymers with unusual architecture such as star polymers and block copolymers and living cationic polymerization is therefore as such of commercial and academic interest.
Polyelectrolytes that bear both cationic and anionic repeat groups are called polyampholytes. The competition between the acid-base equilibria of these groups leads to additional complications in their physical behavior. These polymers usually only dissolve when sufficient added salt screens the interactions between oppositely charged segments.
Step-growth polymers increase in molecular weight at a very slow rate at lower conversions and reach moderately high molecular weights only at very high conversion (i.e., >95%). Solid state polymerization to afford polyamides (e.g., nylons) is an example of step-growth polymerization. [8]
Polyisoprene of latex rubber is an example of a natural polymer, and the polystyrene of styrofoam is an example of a synthetic polymer. In biological contexts, essentially all biological macromolecules —i.e., proteins (polyamides), nucleic acids (polynucleotides), and polysaccharides —are purely polymeric, or are composed in large part of ...
Polyampholytes are polymers that contain both positively charged (cationic) and negatively charged (anionic) functional groups within the same molecule. Their unique structure allows them to exhibit amphoteric behavior, meaning they can interact with a range of substances depending on the surrounding pH, making them useful in applications like drug delivery, water treatment, and biomaterials.
cationic. Examples: ammoniums: RNH 3 + polar, uncharged groups. Examples are alcohols with large R groups, such as diacyl glycerol (DAG), and oligo ethylene glycol with long alkyl chains. Often, amphiphilic species have several lipophilic parts, several hydrophilic parts, or several of both. Proteins and some block copolymers are such examples.