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Synthesis of Amino Functional Monomers Via Controlled Radical Polymerization

Synthesis of Amino Functional Monomers Via Controlled Radical Polymerization
Author: Xeniya Savelyeva
Publisher:
Total Pages:
Release: 2015
Genre:
ISBN:

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"Controlled radical polymerization (CRP) techniques has allowed the synthesis of numerous polymeric materials with comparable control to that of true "living" techniques without the need for stringent manipulation techniques. The control over chain length, dispersity and composition is desirable in many fields, such as stimuli-responsive (temperature or pH) drug carriers. These thermoresponsive polymers in aqueous media are often characterized by lower critical solution temperature (LCST) behavior, where the polymer becomes insoluble with temperature increases. The LCST can be tuned by the structural features of the constituent monomer, molecular weight, molecular weight distribution and copolymerization with other monomers. Narrow molecular weight distribution is the key factor determining the sharpness needed for determining the LCST, which is often exemplified by the cloud point temperature (CPT). Using CRP techniques, specifically nitroxide mediated polymerization (NMP), with an alkoxyamine unimolecular initiator, 2-([tert-butyl[1-(diethoxyphosphoryl)-2,2-dimethylpropyl]amino]oxy)-2-methylpropanoic acid (BlocBuilder) and an additional free nitroxide (SG1), the effect of controlling comonomer (9-(4-vinylbenzyl)-9H-carbazole (VBK)) on polymerization kinetics of N-(2-methacryloyloxyethyl) pyrrolidone (MAEPYR) and the effect of final copolymer composition on CPT was studied. Adding at least 5 mol% VBK, the dispersity Đ of the poly(MAEPYR-stat-VBK) copolymers was below 1.4. The CPT decreased from 59.0 °C to 49.7 °C with addition of only 1 mol% of VBK in the copolymer, and it can be further fine-tuned by changing the solution concentration and the heating rate. Another CRP technique, reversible addition fragmentation chain-transfer polymerization (RAFT), was applied to homopolymerization of N-(3-methoxypropyl) acrylamide (MPAM) to yield well-defined polymers (with (M_n)− = 14.3 - 25.2 kg mol-1 and low Đ ~ 1.17 - 1.47) needed for precise determination of CPT. Thermoresponsive behaviour of poly(MPAM) in aqueous media revealed CPTs between 73 and 92 °C, unlike other literature reports where the polymers, synthesized by conventional radical polymerization, showed conflicting results regarding their LCST" --


Reversible Deactivation Radical Polymerization

Reversible Deactivation Radical Polymerization
Author: Nikhil K. Singha
Publisher: Walter de Gruyter GmbH & Co KG
Total Pages: 302
Release: 2020-01-20
Genre: Technology & Engineering
ISBN: 3110643693

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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.


Synthesis and Free Radical Polymerization of Amino-functionalized Diene Derivatives

Synthesis and Free Radical Polymerization of Amino-functionalized Diene Derivatives
Author: Lifen Wu
Publisher:
Total Pages: 418
Release: 2000
Genre:
ISBN:

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This thesis describes the synthesis of a series of amino-functionalized diene-based monomers, to produce and modify functional polymer materials. Because of the close relationship of structure and property, it was anticipated that the amino-functionalized diene-based monomers can be used potentially as a third comonomer in modifying existing materials (such as SBR or NBR) or the resulting polymers can be used as additives to make polymer blends with high compatibility. The homopolymers of 2-[(N, N-dialkylamino)methyl]-1,3-butadienes with methyl, ethyl and n-propyl substituents were synthesized via bulk free radical polymerization. For each monomer, the effects of polymerization initiator, initiator concentration and reaction temperature on the final polymer structure, molecular weight and glass transition temperature were examined. Homopolymers of 2-[(N-benzyl-N-methylamino)methyl]-1,3-butadiene (BMAMBD) were successfully made through bulk, solution and emulsion free radical polymerizations. Copolymers of BMAMBD with styrene were synthesized and fully characterized by 1H NMR, 13C NMR, GPC, DSC and TGA.


Sustainable Polymers from Biomass

Sustainable Polymers from Biomass
Author: Chuanbing Tang
Publisher: John Wiley & Sons
Total Pages: 458
Release: 2017-02-21
Genre: Technology & Engineering
ISBN: 352734019X

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Offering a unique perspective summarizing research on this timely important topic around the globe, this book provides comprehensive coverage of how molecular biomass can be transformed into sustainable polymers. It critically discusses and compares a few classes of biomass - oxygen-rich, hydrocarbon-rich, hydrocarbon and non-hydrocarbon (including carbon dioxide) as well as natural polymers - and equally includes products that are already commercialized. A must-have for both newcomers to the field as well as established researchers in both academia and industry.


Controlled/living Radical Polymerization

Controlled/living Radical Polymerization
Author: Krzysztof Matyjaszewski
Publisher: Academic
Total Pages: 444
Release: 2009
Genre: Language Arts & Disciplines
ISBN:

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Recent progress in the field of controlled/living radical polymerization.


Synthesis and Controlled Radical Polymerization of Multifunctional Monomers

Synthesis and Controlled Radical Polymerization of Multifunctional Monomers
Author:
Publisher:
Total Pages:
Release: 2004
Genre:
ISBN:

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Multifunctional monomers on the basis of acryl- and methacryl derivatives were synthesized and different protective groups were used. After polymerization the protective groups were removed by different methods. Various initiators for the NMP of the monomers were synthesized and the reaction conditions were optimized. The results showed that NMP was not a suitable method for multifunctional acryl- and methacryl derivatives to achieve well-defined homopolymers, although it was successful for control of polymerization of styrene and block copolymerization of multifunctional acryl- and methacryl derivatives with alkoxyamine terminated polystyrene. The ATRP of multifunctional acrylates and methacrylates has been successfully performed, as well as the block copolymerization of multifunctional acrylates and methacrylates. Relatively low polydispersities of the corresponding polymers (PD=1.18-1.36) and reasonably high rates of polymerization could be achieved when Me6TREN and PMDETA were used as ligands. However, the ATRP of multifunctional acrylamides and methacrylamides failed. The RAFT-polymerization of styrene, acrylamide and acrylate using BDTB as a CTA and AIBN as an initiator afforded polymers with narrow molecular weight distribution (PD=1.13-1.26). A kinetic investigation and the further synthesis of block copolymers using dithioester-terminated homopolymers as macroCTAs showed that the RAFT polymerization of acrylamide M9b proceeded in a living manner. However, BDTB does not control the reaction of methacrylic monomers, such as methacrylates and methacrylamides. The bulk phase behavior of the block copolymers were examined by means of DSC and the surface behaviors of block copolymers as thin layers were examined with AFM. Two-phase transitions in the block copolymers were observed clearly by DSC, indicative of the appearance of phase separations, which were seen in an AFM image. In conclusion, multifunctional acryl- and methacryl derivatives failed to achieve wel.


Sequence-Controlled Polymers

Sequence-Controlled Polymers
Author: Jean-François Lutz
Publisher: John Wiley & Sons
Total Pages: 532
Release: 2018-04-09
Genre: Technology & Engineering
ISBN: 3527342370

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Edited by a leading authority in the field, the first book on this important and emerging topic provides an overview of the latest trends in sequence-controlled polymers. Following a brief introduction, the book goes on to discuss various synthetic approaches to sequence-controlled polymers, including template polymerization, genetic engineering and solid-phase chemistry. Moreover, monomer sequence regulation in classical polymerization techniques such as step-growth polymerization, living ionic polymerizations and controlled radical polymerizations are explained, before concluding with a look at the future for sequence-controlled polymers. With its unique coverage of this interdisciplinary field, the text will prove invaluable to polymer and environmental chemists, as well as biochemists and bioengineers.


Functional Controlled/Living Radical Polymers

Functional Controlled/Living Radical Polymers
Author: Vivek Mishra
Publisher: LAP Lambert Academic Publishing
Total Pages: 132
Release: 2013
Genre:
ISBN: 9783659355776

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This book gives a good understanding of the progress being made in controlled radical polymerization process. The basic principle of controlled/living radical polymerization is fundamental to the creation of new radical polymerization techniques including atom transfer radical, and reversible addition-fragmentation transfer polymerization. These discoveries bring new life to the field of free radical polymerization; indeed, an abundance of polymer materials with different topologies have been prepared. I hope that this Special Topic on "Functional Controlled/Living Radical Polymers: Synthesis, Kinetics and Physico-chemical Properties" will cultivate new ideas and catalyze discoveries in every reader's laboratory. This book is aimed to provide information related to the newest controlled radical polymerization methodology, ATRP and RAFT, their required components and their advantages and necessities. I demonstrates that how simple molecule selectively arrange as different topology like linear, star, multi arm polymers containing functional groups for various applications.