Chain-growth Click Copolymerization for Synthesis of Branched Copolymers with Tunable Branching Density

In this work, we reported a facile synthesis of (hyper)branched copolymers with tunable degree of branching (DB) via one-pot chain-growth copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions. By using a tri-azido core...

Chemical Modification of Xylan

Our study is part of the general context of valuing by-products from the wood industry, which consists of the chemical modification of xylan by synthesis of branched copolymers such as xylan-g-PLLA. The used xylan is extracted from chestnut and 4-dimethylaminopyridine (DMAP) is the catalyst. In fact, the synthesis of xylan-graft-poly (L-lactide) copolymer starting from natural and renewable resource products xylan and L-lactide is performed under different conditions. The results of the grafting reaction are unfavorable due to longer time because of depolymerization reactions. Another result is the solubility and insolubility of the copolymers synthesized in water. This first result indicates that there is a change in the properties of xylan. Moreover, the solubility of the xylan-g-PLLA copolymers is different from one study to another. Grafting of PLLA onto xylan was confirmed by Fourier transform infrared (FT-IR) and 1HNMR analyzes. The dynamic mechanical analysis showed that the xylan-g-PLLA plastic materials have interesting thermomechanical properties.

Synthesis and Properties of Bioresorbable Block Copolymers of l-Lactide, Glycolide, Butyl Succinate and Butyl Citrate

The paper presents the course of synthesis and properties of a series of block copolymers intended for biomedical applications, mainly as a material for forming scaffolds for tissue engineering. These materials were obtained in the polymerization of l-lactide and copolymerization of l-lactide with glycolide carried out using a number of macroinitiators previously obtained in the reaction of polytransesterification of succinic diester, citric triester and 1,4-butanediol. NMR, FTIR and DSC were used to characterize the materials obtained; wettability and surface free energy were assessed too. Moreover, biological tests, i.e., viability and metabolic activity of MG-63 osteoblast-like cells in contact with synthesized polymers were performed. Properties of obtained block copolymers were controlled by the composition of the polymerization mixture and by the composition of the macroinitiator. The copolymers contained active side hydroxyl groups derived from citrate units present in the polymer chain. During the polymerization of l-lactide in the presence of polyesters with butylene citrate units in the chain, obtained products of the reaction held a fraction of highly branched copolymers with ultrahigh molecular weight. The reason for this observed phenomenon was strong intermolecular transesterification directed to lactidyl side chains, formed as a result of chain growth on hydroxyl groups related to the quaternary carbons of the citrate units. Based on the physicochemical properties and results of biological tests it was found that the most promising materials for scaffolds formation were poly(l-lactide–co–glycolide)–block–poly(butylene succinate–co–butylene citrate)s, especially those copolymers containing more than 60 mol % of lactidyl units.

Synthesis of block copolymers using poly(methyl methacrylate) with unsaturated chain end through kinetic studies

Kinetic studies aided the controlled synthesis of PMMA block copolymers and PMMA branched copolymers from a PMMA containing an unsaturated chain end.

pH-responsive polymeric vesicles from branched copolymers

A new type of branched copolymer, poly(l-lactide)2-b-poly(l-glutamic acid), based on polypeptide PLGA is synthesized by the ring-opening polymerization of N-carboxyanhydride of γ-benzyl-l-glutamate with amino-terminated PLLA2–NH2 and subsequent deprotection.