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Related Concept Videos

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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 generated carbocation,...
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

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,...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

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

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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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The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this species into the...
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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 catalyst, high molecular...

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Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
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Ring-opening polymerization in carnosine under pressure.

Chitra Murli1, A K Mishra, Susy Thomas

  • 1High Pressure and Synchrotron Radiation Physics Division, Bhabha Atomic Research Centre, Mumbai, India. cmurli@barc.gov.in

The Journal of Physical Chemistry. B
|March 30, 2012
PubMed
Summary
This summary is machine-generated.

High pressure experiments reveal carnosine (a dipeptide) undergoes ring-opening polymerization of its imidazole ring above 2.8 GPa. The resulting polymer remains stable when pressure is released.

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Area of Science:

  • Biochemistry
  • Materials Science
  • Physical Chemistry

Background:

  • Carnosine is a naturally occurring dipeptide composed of L-histidine and β-alanine.
  • Understanding the behavior of biomolecules under extreme conditions is crucial for various scientific fields.

Purpose of the Study:

  • To investigate the effects of high pressure on the molecular structure and potential transformations of carnosine.
  • To explore the pressure-induced polymerization of carnosine and its stability.

Main Methods:

  • High pressure Raman scattering experiments were conducted on carnosine.
  • Varying pressure conditions were applied, ranging up to 12 GPa.
  • Raman spectra were analyzed to identify structural changes and polymerization.

Main Results:

  • Pressure-induced ring-opening polymerization of the imidazole ring in carnosine was observed.
  • Polymerization initiated at approximately 2.8 GPa, with significant polymerization occurring by 12 GPa.
  • The polymerized form of carnosine did not exhibit any Raman modes of the ambient phase upon release of pressure.

Conclusions:

  • Carnosine can undergo irreversible polymerization under high pressure conditions.
  • The imidazole ring of carnosine is susceptible to pressure-induced ring-opening polymerization.
  • The resulting polymer is stable at ambient conditions, suggesting potential for novel material applications.