Nanoassemblies formed from amphiphilic pillar[5]arene–rod–coil macromolecules in water for the detection of aliphatic diamines. (March 2022)
- Record Type:
- Journal Article
- Title:
- Nanoassemblies formed from amphiphilic pillar[5]arene–rod–coil macromolecules in water for the detection of aliphatic diamines. (March 2022)
- Main Title:
- Nanoassemblies formed from amphiphilic pillar[5]arene–rod–coil macromolecules in water for the detection of aliphatic diamines
- Authors:
- Lu, Jie
Gou, Xiaoliang
Deng, Yingying
Pei, Yi-Rong
Huang, Zhegang
Jin, Long Yi - Abstract:
- Abstract: An amphiphilic pillar[5]arene–rod–coil macromolecule (H 1 ) composed of pillar[5]arene, biphenyl, and oligo(ethylene oxide) groups, was synthesized, and its applicability as a soft material for detecting aliphatic diamines was verified. Amphiphile H 1 self-assembled into unique nanorings and shows an obvious lower critical solution temperature effect in aqueous solution. Interestingly, nanoaggregates of H 1 exhibit certain aggregate-induced emission properties owing to the presence of ten electron-rich biphenyl units on the upper and lower sides of the pillar[5]arene block. In addition, various nanoassemblies were precisely constructed from H 1, through the addition of small molecules with electron-acceptor units. This implies that charge-transfer interactions and hydrophilic/hydrophobic effects cooperatively influence the morphology of H 1 to form diverse nanoassemblies in water. Moreover, macromolecule H 1 with the pillar[5]arene block has a good ability to form host–guest complexes with aliphatic diamines in water, with high selectivity; this significantly affects the process of supramolecular nanoassembly. Graphical abstract: Image 1 Highlights: The pillar[5]arene-rod-coil amphiphiles self-assemble into unique nanorings. The aggregates with various morphologies were formed by charge transfer interaction. Some strong electron-acceptor compounds were detected by charge transfer interaction. Some alkyl amines were detected by pillar[5]arene-rod-coil amphiphiles inAbstract: An amphiphilic pillar[5]arene–rod–coil macromolecule (H 1 ) composed of pillar[5]arene, biphenyl, and oligo(ethylene oxide) groups, was synthesized, and its applicability as a soft material for detecting aliphatic diamines was verified. Amphiphile H 1 self-assembled into unique nanorings and shows an obvious lower critical solution temperature effect in aqueous solution. Interestingly, nanoaggregates of H 1 exhibit certain aggregate-induced emission properties owing to the presence of ten electron-rich biphenyl units on the upper and lower sides of the pillar[5]arene block. In addition, various nanoassemblies were precisely constructed from H 1, through the addition of small molecules with electron-acceptor units. This implies that charge-transfer interactions and hydrophilic/hydrophobic effects cooperatively influence the morphology of H 1 to form diverse nanoassemblies in water. Moreover, macromolecule H 1 with the pillar[5]arene block has a good ability to form host–guest complexes with aliphatic diamines in water, with high selectivity; this significantly affects the process of supramolecular nanoassembly. Graphical abstract: Image 1 Highlights: The pillar[5]arene-rod-coil amphiphiles self-assemble into unique nanorings. The aggregates with various morphologies were formed by charge transfer interaction. Some strong electron-acceptor compounds were detected by charge transfer interaction. Some alkyl amines were detected by pillar[5]arene-rod-coil amphiphiles in water. … (more)
- Is Part Of:
- Dyes and pigments. Volume 199(2022)
- Journal:
- Dyes and pigments
- Issue:
- Volume 199(2022)
- Issue Display:
- Volume 199, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 199
- Issue:
- 2022
- Issue Sort Value:
- 2022-0199-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-03
- Subjects:
- pillar[5]arene -- Nanoassemblies -- Charge transfer interaction -- Lower critical solution temperature -- Host-guest complex
Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2021.110052 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 20653.xml