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Such a polymerization, is referred to as a rate-retarded RAFT polymerization. The rate of a RAFT polymerization, that is, the rate of conversion of monomer into polymer, mainly depends on the rate of the Propagation reaction (Figure 5) because the rate of initiation and termination are much higher than the rate of propagation.
The CTA for RAFT polymerization must be chosen cautiously because it has an effect on polymer length, chemical composition, rate of the reaction and the number of side reactions that may occur. The mechanism of RAFT begins with a standard initiation step as homolytic bond cleavage of the initiator molecule yields a reactive free radical.
Reversible Addition-Fragmentation Chain-Transfer Polymerization (RAFT): requires a compound that can act as a reversible chain-transfer agent, such as dithio compound. [2] Stable Free Radical Polymerization (SFRP): used to synthesize linear or branched polymers with narrow molecular weight distributions and reactive end groups on each polymer ...
PVP is typically prepared by free radical polymerization of 4-vinylphenol or a protected form of 4-vinylphenol. [1] The protected monomers can be prepared from 4-hydroxybenzaldehyde , by vinylation of phenols, or acylation of polystyrene followed by oxidation at room temperature.
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Living polymerization: A chain polymerization from which chain transfer and chain termination are absent. Note: In many cases, the rate of chain initiation is fast compared with the rate of chain propagation, so that the number of kinetic-chain carriers is essentially constant throughout the polymerization. [3]
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]
In polymer chemistry, chain transfer is a polymerization reaction by which the activity of a growing polymer chain is transferred to another molecule: [1] [2] + + where • is the active center, P is the initial polymer chain, X is the end group, and R is the substituent to which the active center is transferred.