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Related Concept Videos

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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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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Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

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Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
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Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

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Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
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Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

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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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Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
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Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

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The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
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Polymerization boosting cascade energy transfer based on opened glucopyranosyl β-cyclodextrin.

Jie Yu1, Hui Wang1, Xian-Yin Dai1

  • 1College of Chemistry, State Key Laboratory of Elemento-Organic Chemistry, Nankai University, Tianjin 300071, P. R. China. yuliu@nankai.edu.cn.

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Researchers developed an injectable hydrogel from modified cyclodextrin and chitosan. This advanced material enables efficient fluorescence and shows potential for cell imaging applications.

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Activation and Conjugation of Soluble Polysaccharides using 1-Cyano-4-Dimethylaminopyridine Tetrafluoroborate CDAP
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Area of Science:

  • Biomaterials Science
  • Supramolecular Chemistry
  • Polymer Chemistry

Background:

  • Chitosan exhibits clustering-triggered emission (CTE) with potential for fluorescent applications.
  • Cyclodextrins are versatile host molecules for supramolecular assembly.

Purpose of the Study:

  • To fabricate an injectable polysaccharide supramolecular hydrogel.
  • To investigate its utility in energy transfer and cell imaging.

Main Methods:

  • Opened D-glucopyranosyl β-cyclodextrin with four aldehyde groups (ACD) was cross-linked with chitosan (CS).
  • The hydrogel was co-assembled with a triphenylamine derivative (TPA) and encapsulated with Cyanine 5 (Cy5) or Nile blue (NiB).
  • Supramolecular cascade energy transfer was studied.

Main Results:

  • The ACD-CS hydrogel exhibited efficient CTE with a high quantum yield of 32.25%.
  • Successful supramolecular cascade energy transfer was achieved, leading to fluorescence emission at 673 nm or 680 nm.
  • The hydrogel demonstrated potential for cell imaging.

Conclusions:

  • An injectable polysaccharide supramolecular hydrogel was successfully fabricated.
  • The hydrogel facilitates efficient energy transfer and exhibits promising cell imaging capabilities.