Ion-selective molecular inclusion of organic dyes into pH-responsive gel assemblies of zwitterionic surfactants. (10th May 2019)
- Record Type:
- Journal Article
- Title:
- Ion-selective molecular inclusion of organic dyes into pH-responsive gel assemblies of zwitterionic surfactants. (10th May 2019)
- Main Title:
- Ion-selective molecular inclusion of organic dyes into pH-responsive gel assemblies of zwitterionic surfactants
- Authors:
- Morita-Imura, Clara
Sakurai, Yuka
Uchiumi, Anna
Shindo, Hitoshi - Abstract:
- Abstract : The pH-Responsive sol–gel transition of a surfactant gel took place along with ion-selective capture and release of dye molecules. Abstract : Surfactant-based gels have attracted considerable attention for molecular capture applications. Methods to promote selective capture of target molecules based on their molecular discrimination behaviour are one route in the development of gel formulations. In this work, it was demonstrated that highly efficient molecular inclusion and unique molecular discrimination based on the ionicity and/or structure of the target molecules can be realized by adopting a pH-responsive sol–gel transition for molecular capture. The zwitterionic amphiphilic compound C16CA formed pH-responsive gel assemblies, which captured organic dye molecules. It was found that the pH-responsive sol–gel transition contributed to highly efficient molecular capture due to the inclusion of dyes in the hydrophobic inner core of the gel assemblies. It was also found that the amine sites of C16CA discriminated between the ionicity of dye molecules via electrostatic interactions. 1 H NMR analysis revealed that cationic dye molecules were included to a limited extent into the hydrophobic core of the gels, whereas anionic dye molecules were incorporated throughout the hydrophilic and hydrophobic domains. These differences in molecular inclusion capacities highlight the selectivity of molecular capture by the C16CA sol–gel transition. Furthermore, target dyeAbstract : The pH-Responsive sol–gel transition of a surfactant gel took place along with ion-selective capture and release of dye molecules. Abstract : Surfactant-based gels have attracted considerable attention for molecular capture applications. Methods to promote selective capture of target molecules based on their molecular discrimination behaviour are one route in the development of gel formulations. In this work, it was demonstrated that highly efficient molecular inclusion and unique molecular discrimination based on the ionicity and/or structure of the target molecules can be realized by adopting a pH-responsive sol–gel transition for molecular capture. The zwitterionic amphiphilic compound C16CA formed pH-responsive gel assemblies, which captured organic dye molecules. It was found that the pH-responsive sol–gel transition contributed to highly efficient molecular capture due to the inclusion of dyes in the hydrophobic inner core of the gel assemblies. It was also found that the amine sites of C16CA discriminated between the ionicity of dye molecules via electrostatic interactions. 1 H NMR analysis revealed that cationic dye molecules were included to a limited extent into the hydrophobic core of the gels, whereas anionic dye molecules were incorporated throughout the hydrophilic and hydrophobic domains. These differences in molecular inclusion capacities highlight the selectivity of molecular capture by the C16CA sol–gel transition. Furthermore, target dye molecules could be selectively recovered and released from the C16CA gels. … (more)
- Is Part Of:
- New journal of chemistry. Volume 43:Number 22(2019)
- Journal:
- New journal of chemistry
- Issue:
- Volume 43:Number 22(2019)
- Issue Display:
- Volume 43, Issue 22 (2019)
- Year:
- 2019
- Volume:
- 43
- Issue:
- 22
- Issue Sort Value:
- 2019-0043-0022-0000
- Page Start:
- 8465
- Page End:
- 8471
- Publication Date:
- 2019-05-10
- 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/c9nj01335k ↗
- 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:
- 10737.xml