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Branch point in a polymer. Polymer architecture in polymer science relates to the way branching leads to a deviation from a strictly linear polymer chain. [1] Branching may occur randomly or reactions may be designed so that specific architectures are targeted. [1] It is an important microstructural feature.
In polymer chemistry, branching is the regular or irregular attachment of side chains to a polymer's backbone chain. It occurs by the replacement of a substituent (e.g. a hydrogen atom ) on a monomer subunit by another covalently-bonded chain of that polymer; or, in the case of a graft copolymer , by a chain of another type.
In polymer chemistry, ring-opening metathesis polymerization (ROMP) is a type of chain-growth polymerization involving olefin metathesis. [1] The reaction is driven by relieving ring strain in cyclic olefins. [2] A variety of heterogeneous and homogeneous catalysts have been developed for different polymers and mechanisms. [3]
Linear topology is a special topological structure that exclusively has two nodes as the termini without any junction nodes. High-density polyethylene (HDPE) could be regarded as a linear polymer chain with very small amount of branching, the linear topology has been listed below: [9] Linear chains capable of forming intra-chain interactions can fold into a wide range of circuit topologies.
Branch point in a polymer. An important microstructural feature of a polymer is its architecture and shape, which relates to the way branch points lead to a deviation from a simple linear chain. [25] A branched polymer molecule is composed of a main chain with one or more substituent side chains or branches.
An example of chain transfer in styrene polymerization. Here X = Cl and Y = CCl 3. In some chain-growth polymerizations there is also a chain transfer step, in which the growing polymer chain RM n ° takes an atom X from an inactive molecule XY, terminating the growth of the polymer chain: RM n ° + XY → RM n X + Y°.
Graft copolymers are a branched copolymer where the components of the side chain are structurally different than that of the main chain. Graft copolymers containing a larger quantity of side chains are capable of wormlike conformation, compact molecular dimension, and notable chain end effects due to their confined and tight fit structures. [1]
For example, if the atom bearing the positive charge is stabilized by electron-donating groups, polymerization will proceed by the S N 1 mechanism. [20] The cationic species is a heteroatom and the chain grows by the addition of cyclic monomers thereby opening the ring system.