A PHEA-g-PEO well-defined graft copolymer exhibiting the synchronous encapsulation of both hydrophobic pyrene and hydrophilic Rhodamine 6G. Issue 2 (25th November 2016)
- Record Type:
- Journal Article
- Title:
- A PHEA-g-PEO well-defined graft copolymer exhibiting the synchronous encapsulation of both hydrophobic pyrene and hydrophilic Rhodamine 6G. Issue 2 (25th November 2016)
- Main Title:
- A PHEA-g-PEO well-defined graft copolymer exhibiting the synchronous encapsulation of both hydrophobic pyrene and hydrophilic Rhodamine 6G
- Authors:
- Sun, Fangxu
Lu, Guolin
Feng, Chun
Li, Yongjun
Huang, Xiaoyu - Abstract:
- Abstract : This article reports the synthesis of a well-defined PHEA- g -PEO graft copolymer by the combination of RAFT polymerization, Cu(i )-mediated ATNRC, and the grafting-onto strategy, which could encapsulate hydrophilic R6G and hydrophobic pyrene simultaneously. Abstract : A well-defined graft copolymer consisting of a poly(2-hydroxyethyl acrylate) (PHEA) backbone and poly(ethylene oxide) (PEO) side chains was synthesized by successive reversible addition–fragmentation chain transfer (RAFT) polymerization and atom transfer nitroxide radical coupling (ATNRC) reaction. RAFT homopolymerization of a Cl-containing acrylate monomer, 2-hydroxyethyl 2-((2-chloropropanoyloxy)methyl)acrylate (HECPMA), was first performed in a controlled way to afford a well-defined PHEA-based backbone with a low polydispersity ( M w / M n = 1.08). The target poly(2-hydroxyethyl acrylate)- g -poly(ethylene oxide) (PHEA- g -PEO) graft copolymer with a narrow molecular weight distribution ( M w / M n = 1.16) was then obtained by ATNRC reaction between the pendant –OCOCH(CH3 )Cl group in every repeated unit of PHEA-based backbone and PEO with a TEMPO end group via the grafting-onto strategy, using CuCl/PMDETA as a catalytic system. The critical micelle concentrations (cmcs) of the obtained graft copolymer in pure water, brine, and aqueous Na2 SO4 solution were determined by the fluorescence probe technique using N -phenyl-1-naphthylamine as probe and micellar morphologies in aqueous media wereAbstract : This article reports the synthesis of a well-defined PHEA- g -PEO graft copolymer by the combination of RAFT polymerization, Cu(i )-mediated ATNRC, and the grafting-onto strategy, which could encapsulate hydrophilic R6G and hydrophobic pyrene simultaneously. Abstract : A well-defined graft copolymer consisting of a poly(2-hydroxyethyl acrylate) (PHEA) backbone and poly(ethylene oxide) (PEO) side chains was synthesized by successive reversible addition–fragmentation chain transfer (RAFT) polymerization and atom transfer nitroxide radical coupling (ATNRC) reaction. RAFT homopolymerization of a Cl-containing acrylate monomer, 2-hydroxyethyl 2-((2-chloropropanoyloxy)methyl)acrylate (HECPMA), was first performed in a controlled way to afford a well-defined PHEA-based backbone with a low polydispersity ( M w / M n = 1.08). The target poly(2-hydroxyethyl acrylate)- g -poly(ethylene oxide) (PHEA- g -PEO) graft copolymer with a narrow molecular weight distribution ( M w / M n = 1.16) was then obtained by ATNRC reaction between the pendant –OCOCH(CH3 )Cl group in every repeated unit of PHEA-based backbone and PEO with a TEMPO end group via the grafting-onto strategy, using CuCl/PMDETA as a catalytic system. The critical micelle concentrations (cmcs) of the obtained graft copolymer in pure water, brine, and aqueous Na2 SO4 solution were determined by the fluorescence probe technique using N -phenyl-1-naphthylamine as probe and micellar morphologies in aqueous media were visualized by TEM. It was found that PHEA- g -PEO graft copolymer self-assembled into large compound micelles in aqueous media, which can encapsulate hydrophilic Rhodamine 6G and hydrophobic pyrene separately or simultaneously. … (more)
- Is Part Of:
- Polymer chemistry. Volume 8:Issue 2(2017)
- Journal:
- Polymer chemistry
- Issue:
- Volume 8:Issue 2(2017)
- Issue Display:
- Volume 8, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 8
- Issue:
- 2
- Issue Sort Value:
- 2017-0008-0002-0000
- Page Start:
- 431
- Page End:
- 440
- Publication Date:
- 2016-11-25
- Subjects:
- Polymers -- Periodicals
Macromolecules -- Periodicals
Polymerization -- Periodicals
547.705 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/PY/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6py01595f ↗
- Languages:
- English
- ISSNs:
- 1759-9954
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.703400
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2306.xml