Post-polymerization modification reactions of poly (glycidyl methacrylate) s
EM Muzammil, A Khan, MC Stuparu - RSC advances, 2017 - pubs.rsc.org
Post-polymerisation modification of poly (glycidyl methacrylate)(PGMA) through the
nucleophilic ring opening reactions of the pendent epoxide groups allows for the installation …
nucleophilic ring opening reactions of the pendent epoxide groups allows for the installation …
Thiol‐epoxy “click” chemistry: Application in preparation and postpolymerization modification of polymers
MC Stuparu, A Khan - Journal of Polymer Science Part A …, 2016 - Wiley Online Library
Base‐catalyzed reaction between a thiol and an epoxide group is a simple fusion process
that leads to the formation of a β‐hydroxythio‐ether linkage. This reaction is efficient, regio …
that leads to the formation of a β‐hydroxythio‐ether linkage. This reaction is efficient, regio …
Homopolymer bifunctionalization through sequential thiol–epoxy and esterification reactions: an optimization, quantification, and structural elucidation study
In this study, we probe various aspects of a post-polymerization double-modification strategy
involving sequential thiol–epoxy and esterification reactions for the preparation of dual …
involving sequential thiol–epoxy and esterification reactions for the preparation of dual …
Step-Growth Glycopolymers with a Defined Tacticity for Selective Carbohydrate–Lectin Recognition
Glycopolymers are potent candidates for biomedical applications by exploiting multivalent
carbohydrate–lectin interactions. Owing to their specific recognition capabilities …
carbohydrate–lectin interactions. Owing to their specific recognition capabilities …
Thiol‐epoxy polymerization via an AB monomer: Synthetic access to high molecular weight poly (β‐hydroxythio‐ether) s
ABSTRACT A synthetic route is developed for the preparation of an AB‐type of monomer
carrying an epoxy and a thiol group. Base‐catalyzed thiol‐epoxy polymerization of this …
carrying an epoxy and a thiol group. Base‐catalyzed thiol‐epoxy polymerization of this …
Synthesis of comb-type amphiphilic graft copolymers derived from chlorinated poly (ɛ-caprolactone) via click reaction
This work refers to the synthesis of a series of novel chlorinated poly (ɛ-caprolactone)(PCL)
for further functionalization of PCL. For this aim, chlorine gas was passed through into the …
for further functionalization of PCL. For this aim, chlorine gas was passed through into the …
Thiol-benzoxazine chemistry as a novel Thiol-X reaction for the synthesis of block copolymers
A novel synthetic procedure is reported for the preparation of block copolymers by means of
successive 1, 3-benzoxazine-thiol and Husigen type azide-alkyne coupling methodologies …
successive 1, 3-benzoxazine-thiol and Husigen type azide-alkyne coupling methodologies …
One‐Pot, One‐Step strategy for the preparation of clickable melamine based microporous organic polymer network
Although, current preparation methods for microporous organic polymers (MOP) based on
coupling or condensations reactions are simple and flexible, they suffer from the …
coupling or condensations reactions are simple and flexible, they suffer from the …
Imidazole-substituted ROMP polymers: Post-modification of poly (norbornenediester) derivatives with aminolysis reactions
BÖ Öztürk, E Yakut, E Ak, SK Şehitoğlu - Reactive and Functional Polymers, 2017 - Elsevier
In this study, ring-opening metathesis polymerization (ROMP) polymers bearing imidazole
and morpholine functionalities were synthesized using an efficient and inexpensive post …
and morpholine functionalities were synthesized using an efficient and inexpensive post …
Kraft pulp–starch covalent linking: A promising route to a new material
PH Elchinger, H Awada, C Zerrouki… - Industrial & …, 2014 - ACS Publications
We reported herein, the synthesis process of a direct cross-linking of modified
polysaccharides. azidated starch, and alkyne Kraft pulp were cross-linked in the presence of …
polysaccharides. azidated starch, and alkyne Kraft pulp were cross-linked in the presence of …