Assignment of the Absolute‐Handedness Chirality of Single‐Walled Carbon Nanotubes Using Organic Molecule Supramolecular Structures. Issue 8 (20th December 2018)
- Record Type:
- Journal Article
- Title:
- Assignment of the Absolute‐Handedness Chirality of Single‐Walled Carbon Nanotubes Using Organic Molecule Supramolecular Structures. Issue 8 (20th December 2018)
- Main Title:
- Assignment of the Absolute‐Handedness Chirality of Single‐Walled Carbon Nanotubes Using Organic Molecule Supramolecular Structures
- Authors:
- Abd El‐Mageed, Ahmed I. A.
Handayani, Murni
Chen, Zhijin
Inose, Tomoko
Ogawa, Takuji - Abstract:
- Abstract: Supramolecular structures of organic molecules on planar nanocarbon surfaces, such as highly oriented pyrolytic graphite (HOPG), have been extensively studied and the factors that control them are generally well‐established. In contrast, the properties of supramolecular structures on curved nanocarbon surfaces like carbon nanotubes remain challenging to predict and/or to understand. This paper reports an investigation into the first study of the supramolecular structures of 5, 15‐bisdodecylporphyrin (C12P) on chiral, concentrated single‐walled carbon nanotubes (SWNTs; with right‐handed helix P ‐ and left‐handed helix M ‐) surfaces using STM. Furthermore, the study is the first of its kind to experimentally assign the absolute‐handedness chirality of SWNTs, as well as to understand their effect on the supramolecular structures of organic molecules on their surfaces. Interestingly, these SWNT enantiomers resulted in supramolecular structures of opposite chirality based on the handedness chirality. With molecular modelling, we predicted the absolute‐handedness chirality of SWNTs, before demonstrating this experimentally. Abstract : By using the STM imaging technique, the single‐walled carbon nanotube (SWNT) absolute‐handedness of chirality has been experimentally investigated using supramolecular structures of porphyrin derivatives (C12P). Two opposite chiral supramolecular structures have been observed based on the SWNT enantiomers handedness of chirality (seeAbstract: Supramolecular structures of organic molecules on planar nanocarbon surfaces, such as highly oriented pyrolytic graphite (HOPG), have been extensively studied and the factors that control them are generally well‐established. In contrast, the properties of supramolecular structures on curved nanocarbon surfaces like carbon nanotubes remain challenging to predict and/or to understand. This paper reports an investigation into the first study of the supramolecular structures of 5, 15‐bisdodecylporphyrin (C12P) on chiral, concentrated single‐walled carbon nanotubes (SWNTs; with right‐handed helix P ‐ and left‐handed helix M ‐) surfaces using STM. Furthermore, the study is the first of its kind to experimentally assign the absolute‐handedness chirality of SWNTs, as well as to understand their effect on the supramolecular structures of organic molecules on their surfaces. Interestingly, these SWNT enantiomers resulted in supramolecular structures of opposite chirality based on the handedness chirality. With molecular modelling, we predicted the absolute‐handedness chirality of SWNTs, before demonstrating this experimentally. Abstract : By using the STM imaging technique, the single‐walled carbon nanotube (SWNT) absolute‐handedness of chirality has been experimentally investigated using supramolecular structures of porphyrin derivatives (C12P). Two opposite chiral supramolecular structures have been observed based on the SWNT enantiomers handedness of chirality (see figure). … (more)
- Is Part Of:
- Chemistry. Volume 25:Issue 8(2019)
- Journal:
- Chemistry
- Issue:
- Volume 25:Issue 8(2019)
- Issue Display:
- Volume 25, Issue 8 (2019)
- Year:
- 2019
- Volume:
- 25
- Issue:
- 8
- Issue Sort Value:
- 2019-0025-0008-0000
- Page Start:
- 1941
- Page End:
- 1948
- Publication Date:
- 2018-12-20
- Subjects:
- absolute-handedness chirality -- porphyrins -- scanning tunneling microscopy -- single-walled carbon nanotubes -- supramolecular structures
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201804832 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11523.xml