Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.7K
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,...
2.7K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.6K
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...
2.6K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

3.0K
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...
3.0K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

2.3K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
2.3K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

4.1K
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...
4.1K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

10.0K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
10.0K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Benzohexacene guide in accurate determination of field effect carrier mobilities in long acenes.

RSC advances·2022
Same author

Single organic molecules for photonic quantum technologies.

Nature materials·2021
Same author

Generic nature of long-range repulsion mechanism on a bulk insulator?

Faraday discussions·2017
Same author

Bicomponent hydrogen-bonded nanostructures formed by two complementary molecular Landers on Au(111).

Chemical communications (Cambridge, England)·2014
Same author

STM imaging, spectroscopy and manipulation of a self-assembled PTCDI monolayer on epitaxial graphene.

Physical chemistry chemical physics : PCCP·2013
Same author

The paradox of an insulating contact between a chemisorbed molecule and a wide band gap semiconductor surface.

Physical chemistry chemical physics : PCCP·2011
Same journal

Quantum simulations of the ballistic motion of a surface adsorbate.

Physical chemistry chemical physics : PCCP·2026
Same journal

Enhancement of triplet-triplet annihilation upconversion in organically modified clay colloids.

Physical chemistry chemical physics : PCCP·2026
Same journal

What is so special about benzene? A comparison of selected carbon and silicon isomers E<sub>6</sub>H<sub>6</sub> (E = C, Si).

Physical chemistry chemical physics : PCCP·2026
Same journal

Synergistic effects of porosity and sulfur doping on hard carbon for superior sodium-ion storage.

Physical chemistry chemical physics : PCCP·2026
Same journal

Force-resolved and recurrence-based identification of dynamical heterogeneity in liquid water.

Physical chemistry chemical physics : PCCP·2026
Same journal

Thermoelectric properties of layered Bi<sub>2</sub>YO<sub>4</sub>Br: a cageless rattler host structure.

Physical chemistry chemical physics : PCCP·2026
See all related articles

Related Experiment Video

Updated: Mar 1, 2026

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

8.5K

Diacetylene polymerization on a bulk insulator surface.

A Richter1, V Haapasilta, C Venturini

  • 1Institute of Physical Chemistry, Johannes Gutenberg University Mainz, 55099 Mainz, Germany. kuehnle@uni-mainz.de.

Physical Chemistry Chemical Physics : PCCP
|June 1, 2017
PubMed
Summary
This summary is machine-generated.

Diacetylene polymerization successfully created conductive polymer chains on insulating calcite surfaces. This breakthrough enables molecular electronics by providing reliable connections for functional molecules on bulk insulators.

More Related Videos

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
06:49

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

Published on: April 22, 2016

12.5K
Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
07:28

Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization

Published on: November 27, 2015

13.9K

Related Experiment Videos

Last Updated: Mar 1, 2026

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

8.5K
Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
06:49

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

Published on: April 22, 2016

12.5K
Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
07:28

Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization

Published on: November 27, 2015

13.9K

Area of Science:

  • Materials Science
  • Nanoscience
  • Surface Chemistry

Background:

  • Molecular electronics offers a path beyond silicon limitations.
  • Connecting functional molecules with conductive polymer chains is crucial for device fabrication.
  • On-surface polymerization is a promising strategy for creating these connections.

Purpose of the Study:

  • To demonstrate diacetylene polymerization on bulk insulator surfaces.
  • To investigate the formation of conductive polymer chains on calcite.
  • To enable future molecular electronic device fabrication on insulating substrates.

Main Methods:

  • Deposition of 3,3'-(1,3-butadiyne-1,4-diyl)bisbenzoic acid precursors on calcite (10.4) surface.
  • In-situ observation using dynamic atomic force microscopy (AFM).
  • Computational analysis using density functional theory (DFT).

Main Results:

  • Ordered molecular islands with a (1 × 3) superstructure formed at room temperature.
  • Heating to 485 K induced the formation of molecular stripes consistent with diacetylene polymers.
  • DFT calculations confirmed the polymerization mechanism and bonding patterns.

Conclusions:

  • Diacetylene polymerization is feasible on bulk insulator surfaces like calcite.
  • This method provides a route to create conductive polymer connections for molecular electronics.
  • The findings pave the way for application-relevant molecular electronic systems.