Phase behaviors and self-assembled properties of ion-pairing amphiphile molecules formed by medium-chain fatty acids and l-arginine triggered by external conditions. (2nd November 2017)
- Record Type:
- Journal Article
- Title:
- Phase behaviors and self-assembled properties of ion-pairing amphiphile molecules formed by medium-chain fatty acids and l-arginine triggered by external conditions. (2nd November 2017)
- Main Title:
- Phase behaviors and self-assembled properties of ion-pairing amphiphile molecules formed by medium-chain fatty acids and l-arginine triggered by external conditions
- Authors:
- Wang, Yuxian
Jiang, Ling
Wei, Ce
Zhang, Hongman - Abstract:
- Abstract : The responsive self-assembled structures of ion-pairing amphiphile molecules will provide good insights into various fields. Abstract : Fatty acids, composed of an amphiphilic carbon chain and a carboxyl group, are a simple class of anion surfactants when they are protonated in the presence of an alkali. They can form ion-pairing amphiphile molecules and self-assemble into different nanostructures, which can be widely applied. However, the phase transition of these nanostructures can be easily triggered by external conditions, such as pH, temperature, the addition of salts and so on. In this work, medium-chain fatty acids (MCFAs) containing 8–12 carbons were chosen as the objects for self-assembly with organic amino counter-ions, l -arginine. We investigated the effects of chain length, pH, temperature and solvent on the phase transition based on diagrams, which could be determined by freeze fracture transmission electron microscopy (FF-TEM) and polarizing microscopy observations (PMO) combined with rheological properties. The results showed that rich phase behavior was observed in the octanoic acid (C8:0) system. However, it was insensitive to changes in pH because of the lower hydrophobicity. In contrast, for decanoic acid (C10:0) and lauric acid (C12:0) systems, phase transition from the L1 phase (micelles) to the Lα phase (vesicles) was observed and they showed stimulus-response to the change of pH. At the same time, lauric acid was sensitive to temperature,Abstract : The responsive self-assembled structures of ion-pairing amphiphile molecules will provide good insights into various fields. Abstract : Fatty acids, composed of an amphiphilic carbon chain and a carboxyl group, are a simple class of anion surfactants when they are protonated in the presence of an alkali. They can form ion-pairing amphiphile molecules and self-assemble into different nanostructures, which can be widely applied. However, the phase transition of these nanostructures can be easily triggered by external conditions, such as pH, temperature, the addition of salts and so on. In this work, medium-chain fatty acids (MCFAs) containing 8–12 carbons were chosen as the objects for self-assembly with organic amino counter-ions, l -arginine. We investigated the effects of chain length, pH, temperature and solvent on the phase transition based on diagrams, which could be determined by freeze fracture transmission electron microscopy (FF-TEM) and polarizing microscopy observations (PMO) combined with rheological properties. The results showed that rich phase behavior was observed in the octanoic acid (C8:0) system. However, it was insensitive to changes in pH because of the lower hydrophobicity. In contrast, for decanoic acid (C10:0) and lauric acid (C12:0) systems, phase transition from the L1 phase (micelles) to the Lα phase (vesicles) was observed and they showed stimulus-response to the change of pH. At the same time, lauric acid was sensitive to temperature, which was ascribed to the higher Krafft point. Besides, when the solvent was replaced by glycerin, phase transitions occurred from vesicles to micelles in these three systems. We hope that this phase transition observed in the MCFA system will provide a good insight into drug delivery, material science, and other related areas. … (more)
- Is Part Of:
- New journal of chemistry. Volume 41:Number 23(2017)
- Journal:
- New journal of chemistry
- Issue:
- Volume 41:Number 23(2017)
- Issue Display:
- Volume 41, Issue 23 (2017)
- Year:
- 2017
- Volume:
- 41
- Issue:
- 23
- Issue Sort Value:
- 2017-0041-0023-0000
- Page Start:
- 14486
- Page End:
- 14497
- Publication Date:
- 2017-11-02
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c7nj03299d ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5412.xml