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Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.4K
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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¹H NMR: Long-Range Coupling01:27

¹H NMR: Long-Range Coupling

1.8K
The coupling interactions of nuclei across four or more bonds are usually weak, with J values less than 1 Hz. While these are usually not observed in spectra, the presence of multiple bonds along the coupling pathway can result in observable long-range coupling.
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene...
1.8K
Phase Transitions02:31

Phase Transitions

19.2K
Whether solid, liquid, or gas, a substance's state depends on the order and arrangement of its particles (atoms, molecules, or ions). Particles in the solid pack closely together, generally in a pattern. The particles vibrate about their fixed positions but do not move or squeeze past their neighbors. In liquids, although the particles are closely spaced, they are randomly arranged. The position of the particles are not fixed—that is, they are free to move past their neighbors to...
19.2K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.1K
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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Phase Transitions: Melting and Freezing02:39

Phase Transitions: Melting and Freezing

12.5K
Heating a crystalline solid increases the average energy of its atoms, molecules, or ions, and the solid gets hotter. At some point, the added energy becomes large enough to partially overcome the forces holding the molecules or ions of the solid in their fixed positions, and the solid begins the process of transitioning to the liquid state or melting. At this point, the temperature of the solid stops rising, despite the continual input of heat, and it remains constant until all of the solid is...
12.5K
Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

2.9K
Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
2.9K

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Related Experiment Video

Updated: Jul 27, 2025

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
06:55

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level

Published on: September 26, 2016

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Topological phases in coupled polyyne chains.

Nisa Ara1, Rudranil Basu1

  • 1BITS-Pilani, KK Birla Goa Campus, NH 17B, Bypass Road, Zuarinagar, Goa 403726, India.

Journal of Physics. Condensed Matter : an Institute of Physics Journal
|June 5, 2023
PubMed
Summary
This summary is machine-generated.

We investigated topological properties of stacked polyyne chains. Different stacking arrangements exhibit distinct topological phases and edge modes, offering insights into novel electronic behaviors.

Keywords:
bilayer systemcarbon chainsedge modestopological phases

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Area of Science:

  • Condensed Matter Physics
  • Materials Science
  • Quantum Chemistry

Background:

  • Polyyne chains are carbon allotropes with unique electronic properties.
  • Topological materials exhibit exotic electronic states protected by symmetry.
  • Understanding stacking effects is crucial for designing novel electronic devices.

Purpose of the Study:

  • To investigate the topological electronic properties of coupled parallel polyyne chains.
  • To analyze the impact of different stacking arrangements (AA and AB) on topological phases.
  • To explore the existence and characteristics of edge modes in these systems.

Main Methods:

  • Tight-binding Hamiltonians parameterized using first-principles calculations.
  • Topological classification using the BDI class scheme.
  • Calculation of topological invariants and edge mode analysis.

Main Results:

  • Both AA and AB stacking arrangements fall within the BDI topological class.
  • AA stacking exhibits one topological phase for both metallic and insulating states.
  • AB stacking shows two distinct topological phases, with transitions requiring significant strain.
  • Four non-zero energy edge modes found in AA stacking; two zero-energy edge modes in AB stacking.

Conclusions:

  • Stacking configuration significantly influences the topological properties of polyyne chains.
  • The identified topological phases and edge modes offer potential for novel electronic applications.
  • Strain engineering in AB stacking could unlock transitions between distinct topological phases.