Related Experiment Video
Updated: Feb 22, 2026

09:28
Engineering Molecular Recognition with Bio-mimetic Polymers on Single Walled Carbon Nanotubes
Published on: January 10, 2017
8.6K
Intrinsic Chirality Origination in Carbon Nanotubes
Neal Pierce1, Gugang Chen1, Lakshmy P Rajukumar1,2
1Honda Research Institute USA Inc. , Columbus, Ohio 43212, United States.
ACS Nano
|September 28, 2017
Summary
Understanding carbon nanotube chirality is crucial. This study reveals that carbon nuclei have an intrinsic preference for specific chiralities, independent of catalyst structure, influencing nanotube growth.
Area of Science:
- Materials Science
- Nanotechnology
- Chemical Engineering
Background:
- Controlling carbon nanotube (CNT) chirality is essential for harnessing their unique properties.
- Existing theories often attribute CNT chirality to the epitaxial relationship with catalyst structures.
Purpose of the Study:
- To investigate the intrinsic factors governing carbon nanotube chirality.
- To differentiate the influence of intrinsic carbon nucleation preferences from catalyst-induced effects on chirality.
Main Methods:
- Grew carbon nanotubes on floating liquid gallium (Ga) droplets to eliminate catalyst structure influence.
- Compared chirality abundances from liquid Ga droplet growth with those from solid ruthenium (Ru) nanoparticle catalysts.
- Analyzed chirality abundances in relation to nucleation probability, considering the Zeldovich factor and deviation from critical size.
Main Results:
- Growth on liquid Ga droplets demonstrated an intrinsic preference of carbon nuclei for specific chiralities, independent of catalyst morphology.
- Observed significant differences in chirality abundance between liquid and solid catalyst systems.
- Found that while some chiralities showed strong intrinsic preference (e.g., (11,1) over (9,4) for same diameter), others fluctuated with temperature on liquid droplets, suggesting a combined effect.
Conclusions:
- CNT chirality arises from an interplay between the intrinsic preference of carbon clusters and external induction by catalyst structure.
- Liquid catalyst droplets offer a promising route for exploring intrinsic chirality preferences.
- Findings pave the way for developing strategies for chirality-selective synthesis of carbon nanotubes.
Related Concept Videos
Prochirality
5.1K
The concept of prochirality leads to the nomenclature of the individual faces of a molecule and plays a crucial role in the enantioselective reaction. It is a concept where two or more achiral molecules react to produce chiral products. A typical process is the reaction of an achiral ketone to generate a chiral alcohol. Here, the achiral reactant reacts with an achiral reducing agent, sodium borohydride, to generate an equimolar mixture of the chiral enantiomers of the product. For example, an...
5.1K
Chirality in Nature
17.4K
Chirality is the most intriguing yet essential facet of nature, governing life’s biochemical processes and precision. It can be observed from a snail shell pattern in a macroscopic world to an amino acid, the minutest building block of life. Most of the snails around the world have right-coiled shells because of the intrinsic chirality in their genes. All the amino acids present in the human body exist in an enantiomerically pure state, except for glycine - the sole achiral amino acid.
17.4K
Chirality at Nitrogen, Phosphorus, and Sulfur
7.1K
Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
A consequence of chirality is the need for enantiomeric resolution. While this is theoretically possible for all...
7.1K
Chirality
30.0K
Chirality is a term that describes the lack of mirror symmetry in an object. In other words, chiral objects cannot be superposed on their mirror images. For example, our feet are chiral, as the mirror image of the left foot, the right foot, cannot be superposed on the left foot.
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
Chiral objects exhibit a sense of handedness when they interact with another chiral object. For example, our left foot can only fit in the left shoe and not in the right shoe. Achiral objects — objects that have...
30.0K
Radicals: Electronic Structure and Geometry
5.2K
This lesson delves into the geometry of a radical, which is influenced by the electronic structure of the molecule. The principle is similar to that of a lone pair, where the unpaired electron influences the geometry at the radical center.
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
5.2K
Molecules with Multiple Chiral Centers
15.3K
Molecules that possess multiple chiral centers can afford a large number of stereoisomers. For instance, while some molecules like 2-butanol have one chiral center, defined as a tetrahedral carbon atom with four different substituents attached, several molecules like butane-2,3-diol have multiple chiral centers. A simple formula to predict the number of stereoisomers possible for a molecule with n chiral centers is 2n. However, there can be a lower number where some of the stereoisomers are...
15.3K

