21.9
ラジカル連鎖重合のメカニズムは、重合の開始、伝播、終了の 3 つのステップで構成されます。 ラジカル開始剤から発生したフリーラジカルがモノマーの不飽和結合に付加すると、重合が始まります。 フリーラジカルの不対電子と不飽和結合の 1 つの π 電子により、フリーラジカルとモノマーの間に σ 結合が形成…
ラジカル連鎖成長重合は、開始、増殖、終了の3つの段階で構成されています。
開始ステップでは、ラジカル開始剤のホモリシス核分裂によって生成されたフリーラジカルがモノマーの二重結合と反応します。これは、開始剤とモノマーとの間にシグマ結合を生成します。その結果、ラジカル部位はモノマーに移動します。
この増殖ステップは、この新しいラジカル種が別のモノマーに加わることから始まります。このステップを繰り返して、ポリマー鎖を成長させるためにモノマーを追加します。
モノマーは優先的に結合するため、ラジカル部位は常により置換された炭素上に存在する。
最後に、鎖の終結は、成長する2つのポリマー鎖のラジカルの結合によって発生する可能性があります。
あるいは、一方の鎖のラジカルは、もう一方のポリマー鎖のラジカル部位に隣接する炭素から水素を分離します。したがって、重合が停止し、アルキル末端ポリマーとアルケニル末端ポリマーのペアが得られます。
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Q1: What happens during the initiation step of radical chain-growth polymerization?
During initiation, a free radical generated from a radical initiator undergoes homolytic fission and reacts with the monomer's double bond. This creates a sigma bond between the initiator and monomer, shifting the radical site to the newly bonded monomer. This activated monomer is now ready to begin the propagation phase of polymerization.
Q2: How does the propagation step build the polymer chain?
During propagation, the radical species adds to another monomer's unsaturated bond, creating a new radical site on the freshly added monomer. This step repeats cyclically, with each addition extending the polymer chain. The number of propagation cycles directly determines the final molecular weight of the polymer chain produced.
Q3: Why do monomers add in a head-to-tail manner during radical polymerization?
Monomers preferentially bond such that the radical site remains on the more substituted carbon. In monosubstituted monomers like vinyl chloride and styrene, this positioning places the unpaired electron on the substituted carbon (tail), stabilizing the growing chain and favoring head-to-tail addition throughout polymerization.
Q4: What are the two main pathways for terminating radical polymerization?
Termination occurs through radical coupling, where two growing chains' radical sites combine directly, or through radical disproportionation, where one chain's radical abstracts hydrogen from the other chain's alpha carbon. Coupling produces a single chain with a saturated bond, while disproportionation yields one alkyl-terminated and one alkenyl-terminated polymer.
Q5: How does radical disproportionation differ from radical coupling in chain termination?
In radical coupling, two radical sites bond directly to form a single polymer with a saturated linkage. In radical disproportionation, one radical abstracts hydrogen from the alpha carbon of another chain, producing two distinct polymers: one ending in an alkyl group and one ending in an alkenyl group.
Q6: What role do chain transfer reagents play in radical polymerization termination?
Chain transfer reagents terminate polymer chain growth by removing the radical site from the growing chain or reducing its reactivity. Unlike coupling and disproportionation, chain transfer does not eliminate the radical entirely but instead transfers it elsewhere, allowing polymerization to continue on a new chain or with reduced efficiency.
Q7: How does radical chain-growth polymerization compare to other polymerization mechanisms?
Radical chain-growth polymerization uses free radicals to initiate and propagate chain growth through three distinct stages. Other mechanisms like anionic chain-growth polymerization and cationic chain-growth polymerization employ different reactive intermediates and initiation strategies, offering alternative pathways for synthesizing polymers with distinct properties.