Poly(2-isopropenyl-2-oxazoline) – a structural analogue to poly(vinyl azlactone) with Orthogonal Reactivity-Reference-Cited by-同舟云学术

Poly(2-isopropenyl-2-oxazoline) – a structural analogue to poly(vinyl azlactone) with Orthogonal Reactivity

Published:2020 Issue:35 Volume:11 Page:5681-5692
ISSN:1759-9954
Container-title:Polymer Chemistry
language:en
Short-container-title:Polym. Chem.

Author:

Leiske Meike N.¹²³⁴⁵^ORCID,Mahmoud Ayaat M.¹²³⁴⁵,Warne Nicole M.¹²³⁴⁵,Goos Jeroen A. C. M.¹²³⁴⁵,Pascual Sagrario⁶⁷⁸⁹^ORCID,Montembault Véronique⁶⁷⁸⁹^ORCID,Fontaine Laurent⁶⁷⁸⁹^ORCID,Davis Thomas P.¹²³⁴⁵^ORCID,Whittaker Michael R.¹²³⁴⁵^ORCID,Kempe Kristian¹²³⁴⁵^ORCID

Affiliation:

1. ARC Centre of Excellence in Convergent Bio-Nano Science & Technology

2. and Drug Delivery

3. Disposition and Dynamics

4. Monash Institute of Pharmaceutical Sciences

5. Monash University

6. Institut des Molécules et Matériaux du Mans (IMMM)

7. UMR 6283 CNRS – Le Mans Université

8. 72085 Le Mans Cedex 9

9. France

Abstract

A modular copolymer platform based on two oxazole derivatives is presented. Post-polymerisation modifications revealed the potential to selectively modify the individual side groups, providing access to functional copolymer libraries in the future.

Funder

Australian Research Council

Alexander von Humboldt-Stiftung

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Polymers and Plastics,Biochemistry,Bioengineering

Link

http://pubs.rsc.org/en/content/articlepdf/2020/PY/D0PY00861C

Reference49 articles.

1. How To Tune the Gene Delivery and Biocompatibility of Poly(2-(4-aminobutyl)-2-oxazoline) by Self- and Coassembly

2. Synthesis of biscarboxylic acid functionalised EDTA mimicking polymers and their ability to form Zr(iv) chelation mediated nanostructures