People | Locations | Statistics |
---|---|---|
Naji, M. |
| |
Motta, Antonella |
| |
Aletan, Dirar |
| |
Mohamed, Tarek |
| |
Ertürk, Emre |
| |
Taccardi, Nicola |
| |
Kononenko, Denys |
| |
Petrov, R. H. | Madrid |
|
Alshaaer, Mazen | Brussels |
|
Bih, L. |
| |
Casati, R. |
| |
Muller, Hermance |
| |
Kočí, Jan | Prague |
|
Šuljagić, Marija |
| |
Kalteremidou, Kalliopi-Artemi | Brussels |
|
Azam, Siraj |
| |
Ospanova, Alyiya |
| |
Blanpain, Bart |
| |
Ali, M. A. |
| |
Popa, V. |
| |
Rančić, M. |
| |
Ollier, Nadège |
| |
Azevedo, Nuno Monteiro |
| |
Landes, Michael |
| |
Rignanese, Gian-Marco |
|
Cammas-Marion, Sandrine
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (5/5 displayed)
- 2024Effect of Formulation Parameters and Physiological Environment on Amlodipine Release Kinetics Encapsulated in Biodegradable Polymers and Optimized by Design Methodology
- 2016Poly(trimethylene carbonate)/Poly(malic acid) Amphiphilic Diblock Copolymers as Biocompatible Nanoparticlescitations
- 2015Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclidescitations
- 2015Development of Biocompatible and Functional Polymeric Nanoparticles for Site-Specific Delivery of Radionuclidescitations
- 2011Metal catalyzed ring-opening polymerization of benzyl malolactonate: a synthetic access to copolymers of β-benzyl malolactonate and trimethylene carbonatecitations
Places of action
Organizations | Location | People |
---|
article
Metal catalyzed ring-opening polymerization of benzyl malolactonate: a synthetic access to copolymers of β-benzyl malolactonate and trimethylene carbonate
Abstract
The "immortal" coordination-insertion ring-opening polymerization of benzyl malolactonate (MLABe) initiated by the two-component catalyst system based on the zinc amide precursor, (BDI)Zn[N(SiMe3)2] (BDI = β-diiminate ligand), and benzyl alcohol (BnOH) acting as a co-initiator and a chain transfer agent proceeds in bulk at 40 °C. Functional telechelic poly(β-benzyl malolactonate)s, H-PMLABe-OBn, are thus obtained. Sequential copolymerization with trimethylene carbonate (TMC) affords block copolymers, PTMC-b-PMLABe, which are alternatively prepared from the chemical coupling of the PMLABe-COOH and PTMC-OH homopolymers. Simultaneous copolymerization of both the lactone and the carbonate monomers offers the PTMC-co-PMLABe random copolymers. The (co)polymers have been characterized by NMR, FT-IR, SEC and DSC analyses. These represent the first examples of β-benzyl malolactonate/carbonate copolymers. More importantly, these (co)polymers could be synthesized free of metallic residues thereby making them suitable as biomedical and pharmaceutical biomaterials.