Functional Polymers Via Post-polymerization Modification of Reactive Polymers Derived from 1,1-disubstituted-2-vinylcyclopropane - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Functional Polymers Via Post-polymerization Modification of Reactive Polymers Derived from 1,1-disubstituted-2-vinylcyclopropane write by Denis Hervé Ntoukam Seuyep. This book was released on 2014. Functional Polymers Via Post-polymerization Modification of Reactive Polymers Derived from 1,1-disubstituted-2-vinylcyclopropane available in PDF, EPUB and Kindle.
Post-polymerization Modification by Direct C-H Functionalization
Post-polymerization Modification by Direct C-H Functionalization - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Post-polymerization Modification by Direct C-H Functionalization write by Di Liu (Ph. D.). This book was released on 2016. Post-polymerization Modification by Direct C-H Functionalization available in PDF, EPUB and Kindle. Post-polymerization modification of polymers is an important tool for accessing macromolecular materials with desired functional groups and tailored properties. Such strategy may become the only route to a target polymer when the availability or reactivity of the corresponding monomer is not suited for direct polymerization. Most post-polymerization modification processes are based on transforming functional groups that are pre-installed in the side chains or chain-ends of a polymer. Despite the excellent efficiency and versatility, they are limited to certain backbone structures and often require additional synthetic effort for the synthesis of the corresponding pre-functionalized monomers. More specifically, they are useful only when the pre-functionalized monomers can be readily prepared and incorporated to a polymer by direct polymerization. In contrast, direct functionalization of C-H bonds along the polymer backbone offers a markedly different strategy for the synthesis of functional polymers. Despite the inert nature, the ubiquity of the C-H bonds and their tunable reactivity make them ideal targets for selective chemical modification. In this dissertation, it is first demonstrated that poly(vinyl ester)s and poly(vinyl ether-co-vinyl ester) can be readily prepared via a ruthenium catalyzed C–H oxyfunctionalization of the corresponding poly(vinyl ether)s under mild conditions. The method can be further applied for the synthesis of high molecular weight poly(propenyl ester)s which cannot be obtained using other methods. In addition the method allows poly(isopropenyl ester) to be synthesized without the use of extremely high pressures. Using a similar strategy poly(ethylene glycol-co-glycolic acid) can be prepared by the ruthenium-catalyzed oxidation of poly(ethylene glycol) (PEG). A new process has been developed so that the transformation will cause little chain degradation. The presence of the hydrolytically labile ester groups in the PEG backbone renders the copolymer biodegradable, which may allow the PEG of higher molecular weight to be used in biomedical applications without the concerns of bioaccumulation of PEG into various organs. Lastly, it is demonstrated that azido-functionalized, isotactic polypropylene can be prepared via the direct C–H azidation of a commercially available polymer using a stable azidoiodinane. The azidated PP can further undergo copper-catalyzed azide-alkyne cycloaddition with alkyne terminated polymer to obtain PP-based graft copolymers. It is expected that the ability to incorporate versatile functional groups, such as azides, into common polyolefin feedstocks should expand their applications and potentially enable the realization of new classes of materials.
Reversible Deactivation Radical Polymerization
Reversible Deactivation Radical Polymerization - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Reversible Deactivation Radical Polymerization write by Nikhil K. Singha. This book was released on 2020-01-20. Reversible Deactivation Radical Polymerization available in PDF, EPUB and Kindle. This book describes strategies and mechanism of reversible deactivation radical polymerization (RDRP) to synthesize functional polymers. Several approaches such as atom transfer radical polymerization and the combination of click chemistry and RDRP are summarized. Contributors from interdisciplinary fields highlight applications in nanotechnology, self-healing materials, oil and water resistant coatings and controlled drug delivery systems.
Reactive Modifiers for Polymers
Reactive Modifiers for Polymers - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Reactive Modifiers for Polymers write by S. Al-Malaika. This book was released on 2012-12-06. Reactive Modifiers for Polymers available in PDF, EPUB and Kindle. Chemical modification of polymers by reactive modifiers is no longer an academic curiosity but a commercial reality that has delivered a diverse range of speciality materials for niche markets: reactively grafted styrenic alloys, maleated polyolefins, super-tough nylons, silane modified and moisture-cured polyolefins, and thermoplastic elastomers, are but few exam ples of commercial successes. Although the approach of reactive modification of polymers has been largely achieved either in solution or in the solid state (through in situ reactions in polymer melts), it is the latter route that has attracted most attention in the last two decades owing to its flexibility and cost-effective ness. This route, referred to as reactive processing, focuses on the use of suitable reactive modifier(s) and the adoption of conventional polymer processing machinery, an extruder or a mixer, as a chemical reactor, to perform in situ targeted reactions for chemical modification of preformed polymers. This relatively simple, though scientifically highly challenging, approach to reactive modification offers unique opportunities in exploiting various reactive modifiers for the purpose of altering and transforming in a controlled manner the properties of preformed commercial polymers into new/speciality materials with tailor-made properties and custom-designed performance for target applications. Such an economically attractive route constitutes a radical diversion away from the traditional practices of manufacturing new polymers from monomers which involves massive in vestments in sophisticated technologies and chemical plants.
Synthesis and Application of Some Novel Functional Polymers Via Controlled Radical Polymerization and Click Chemistry
Synthesis and Application of Some Novel Functional Polymers Via Controlled Radical Polymerization and Click Chemistry - read free eBook in online reader or directly download on the web page. Select files or add your book in reader. Download and read online ebook Synthesis and Application of Some Novel Functional Polymers Via Controlled Radical Polymerization and Click Chemistry write by Guang-Zhao Li. This book was released on 2012. Synthesis and Application of Some Novel Functional Polymers Via Controlled Radical Polymerization and Click Chemistry available in PDF, EPUB and Kindle. The objective of this thesis was to prepare thermoresponsive PEG-based homopolymers and copolymers by combination of cobalt-mediated catalytic chain-transfer polymerization (CCTP) and thiol-ene "click" chemistry and prepare well-defined glycopolymers via "living" polymerization and "click" chemistry. The effect of different catalysts for the nucleophilic mediated thiol-ene reaction was investigated using model compounds, both monomers and oligomers obtained by CCTP. Different catalysts, including pentylamine and hexylamine (primary amines), triethylamine (tertiary amine), and two different phosphines, dimethylphenylphosphine (DMPP) and tris(2-carboxyethyl) phosphine (TCEP), were investigated in the presence of different thiols. The optimum reaction conditions for nucleophile mediated thiol-ene click reactions were investigated. Thermoresponsive PEG-based homopolymers and copolymers of OEGMEMA obtained by CCT were modified using thiol-ene click chemistry with a variety of different functional thiol compounds to yield functional thermoresponsive polymers in high yield. The effect of different solvent systems for based catalyzed thiol-ene reaction was investigated in the presence of different functional thiols. The ATRP polymerization of TMS-PgMA and TIPS-PgMA and ROP polymerization of aliphatic polyester were investigated. A maleimide functional initiator was used in order to achieve post conjugation of nanoparticles for drug delivery. Moreover, the disulfide based bifunctional initiator was introduced into the midpoint of the polymer chain, which could break down to afford the corresponding polymer chain with thiol end group under the reducing condition. The thiol-terminated polymer was also post-functionalized via thiol-ene click chemistry. In addition, the aliphatic polycarbonate is a biocompatible and biodegradable polymer, which is widely used in medical and pharmaceutical applications. The subsequent introduction of sugar moiety to the reactive polymer chain via CuAAC click reaction and then the interactions between glycopolymers and lectins were investigated by Surface Plasmon Resonance (SPR) and Quartz Crystal Microbalance with Dissipation (QCM-D). The controlled SET-LRP polymerization of TMS-PgMA and SET-RAFT polymerization PgMA with the intact alkyne at ambient temperature were investigated. A maleimide functional initiator and CPDB, as the chain transfer agent have been employed. The introduction of maleimide moiety was to allow for post polymerization conjugation to peptides via reaction with cysteines. The subsequent introduction of sugar azides to click with the reactive polymer containing alkyne group and the glycopolymers through CuAAC was also investigated. The glycopolymer has been successfully prepared combining the SET-LRP/SET-RAFT and CuAAc click chemistry at ambient temperature.
