Block copolymers comprising degradable poly(2-ethyl-2-oxazoline) analogues via copper-free click chemistry. Issue 38 (13th September 2021)
- Record Type:
- Journal Article
- Title:
- Block copolymers comprising degradable poly(2-ethyl-2-oxazoline) analogues via copper-free click chemistry. Issue 38 (13th September 2021)
- Main Title:
- Block copolymers comprising degradable poly(2-ethyl-2-oxazoline) analogues via copper-free click chemistry
- Authors:
- Göppert, Natalie E.
Dirauf, Michael
Weber, Christine
Schubert, Ulrich S. - Abstract:
- Abstract : We present the synthesis development of amphiphilic, degradable poly(2-ethyl-2-oxazoline) (PEtOx) analogue block copolymers in a modular fashion utilizing the strain-promoted azide–alkyne cycloaddition (SPAAC). Abstract : We present the synthesis development of amphiphilic, degradable poly(2-ethyl-2-oxazoline) (PEtOx) analogue block copolymers in a modular fashion utilizing the strain-promoted azide–alkyne cycloaddition (SPAAC). Subsequently to preliminary ω-end group oxidation studies by means of matrix-assisted laser desorption ionization mass spectrometry, a clickable, degradable poly(2-ethyl-2-oxazoline- stat -glycine) was synthesized via a three step post-polymerization synthesis procedure comprising the hydrolysis of azido-terminated PEtOx yielding the linear, azido-terminated poly(ethylene imine), the partial oxidation of the polymer backbone to incorporate randomly distributed glycine moieties and the re-introduction of the N -acyl ethylene imine repeating units. The azido ω-end group enabled the utilization in SPAAC. In a proof of concept approach, the degradable PEtOx analogue and its non-degradable relative were attached to a hydrophobic poly(2- n -nonyl-2-oxazoline) as well as a poly(ε-caprolactone) block via SPAAC. The successful conjugations were confirmed by in depth characterization utilizing NMR spectroscopy, size exclusion chromatography and matrix-assisted laser desorption ionization mass spectrometry. Due to its simplicity and flexibility theAbstract : We present the synthesis development of amphiphilic, degradable poly(2-ethyl-2-oxazoline) (PEtOx) analogue block copolymers in a modular fashion utilizing the strain-promoted azide–alkyne cycloaddition (SPAAC). Abstract : We present the synthesis development of amphiphilic, degradable poly(2-ethyl-2-oxazoline) (PEtOx) analogue block copolymers in a modular fashion utilizing the strain-promoted azide–alkyne cycloaddition (SPAAC). Subsequently to preliminary ω-end group oxidation studies by means of matrix-assisted laser desorption ionization mass spectrometry, a clickable, degradable poly(2-ethyl-2-oxazoline- stat -glycine) was synthesized via a three step post-polymerization synthesis procedure comprising the hydrolysis of azido-terminated PEtOx yielding the linear, azido-terminated poly(ethylene imine), the partial oxidation of the polymer backbone to incorporate randomly distributed glycine moieties and the re-introduction of the N -acyl ethylene imine repeating units. The azido ω-end group enabled the utilization in SPAAC. In a proof of concept approach, the degradable PEtOx analogue and its non-degradable relative were attached to a hydrophobic poly(2- n -nonyl-2-oxazoline) as well as a poly(ε-caprolactone) block via SPAAC. The successful conjugations were confirmed by in depth characterization utilizing NMR spectroscopy, size exclusion chromatography and matrix-assisted laser desorption ionization mass spectrometry. Due to its simplicity and flexibility the presented SPAAC approach offers numerous possibilities for the design of block copolymers comprising degradable poly(2-oxazoline) segments. … (more)
- Is Part Of:
- Polymer chemistry. Volume 12:Issue 38(2021)
- Journal:
- Polymer chemistry
- Issue:
- Volume 12:Issue 38(2021)
- Issue Display:
- Volume 12, Issue 38 (2021)
- Year:
- 2021
- Volume:
- 12
- Issue:
- 38
- Issue Sort Value:
- 2021-0012-0038-0000
- Page Start:
- 5426
- Page End:
- 5437
- Publication Date:
- 2021-09-13
- 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/d1py00853f ↗
- 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:
- 19623.xml