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Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

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Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
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Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
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Cationic Chain-Growth Polymerization: Mechanism00:57

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The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
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Anionic Chain-Growth Polymerization: Mechanism01:04

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The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
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Cell size is a significant factor impacting cellular design, function, and fitness. There exists some internal coordination by which cells double their masses before division, thus, achieving homeostasis. Coordination between cell growth and proliferation depends on the checkpoints in between cell cycle phases. Loss of coordination or failure in the checkpoint mechanism can drive the cell to uncontrolled growth and loss of cellular function. Like dividing cells that coordinate cellular growth,...
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Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
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Controlled node growth on the surface of polymersomes.

Marjolaine Thomas1, Spyridon Varlas1, Thomas R Wilks1

  • 1School of Chemistry, University of Birmingham Edgbaston Birmingham B15 2TT UK s.fielden@bham.ac.uk r.oreilly@bham.ac.uk.

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Synthetic polymers functionalized with nucleobases enable controlled self-assembly. Nucleobase pairing directed the formation and growth of surface nodes on polymersomes, creating novel nanomaterials.

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Area of Science:

  • Polymer Chemistry
  • Supramolecular Chemistry
  • Nanotechnology

Background:

  • Nucleobase incorporation into synthetic polymers facilitates controlled self-assembly through hydrogen bonding.
  • This approach allows for the creation of complex particle morphologies.

Purpose of the Study:

  • To utilize nucleobase pairing to direct the formation and growth of surface nodes on polymersomes.
  • To investigate the mechanism of node formation driven by steric crowding.

Main Methods:

  • Functionalizing polymersomes with adenine in membrane-forming domains.
  • Inserting self-assembling diblock copolymers containing thymine into polymersome membranes.
  • Imaging nano-objects using cryo-transmission electron microscopy (cryo-TEM) for quantification.

Main Results:

  • Nucleobase pairing (adenine-thymine) successfully directed node formation and lengthening on polymersome surfaces.
  • Insertion of thymine-containing copolymers induced steric crowding, leading to node initiation and growth.
  • Cryo-TEM enabled quantification of node coverage and length, demonstrating control over growth.

Conclusions:

  • Nucleobase pairing is an effective strategy for controlling the growth of surface features on polymersomes.
  • This method offers a new platform for developing higher-order nanomaterials with tunable properties.