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Synthesis Of Well Defined Cyclic Branched And Water Soluble Polymers Via The Anionic Polymerization Of 2 Vinylpyridine
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Book Synopsis Synthesis of Well-defined Cyclic, Branched, and Water-soluble Polymers Via the Anionic Polymerization of 2-vinylpyridine by : William Toreki
Download or read book Synthesis of Well-defined Cyclic, Branched, and Water-soluble Polymers Via the Anionic Polymerization of 2-vinylpyridine written by William Toreki and published by . This book was released on 1988 with total page 328 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Anionic Synthesis of Well-defined Functionalized and Star-branched Polymers by : Manuela Ocampo
Download or read book Anionic Synthesis of Well-defined Functionalized and Star-branched Polymers written by Manuela Ocampo and published by . This book was released on 2007 with total page 210 pages. Available in PDF, EPUB and Kindle. Book excerpt: Novel methods for the synthesis of chain-end and in-chain functionalized polymers, as well as star polymers, were developed using anionic polymerization techniques. A new mechanism for the reaction of polymeric organolithium compounds with thiiranes has been found. The reaction of poly(styryl)lithium and poly(butadienyl)lithium with propylene sulfide and ethylene sulfide was investigated in hydrocarbon solution for the preparation of thiol-functional polymers. It was found by MALDI-TOF mass spectral analysis of the reaction products that the reaction proceeded by attack of the anion on the methylene carbon atom of the thiirane ring followed by ring opening to form the thiol-functionalized polymer. The reaction of poly(styryl)lithium with trimethylene sulfide did not produce the corresponding thiol-functionalized polymer; the resulting methyl-terminated polymer was formed by attack of the anion on the sulfur atom followed by ring opening to form a primary carbanion. A new method for synthesis of alkoxysilyl-functionalized polymers was developed. Using a general functionalization methodology based on the hydrosilation of vinyltrimethoxysilane with [omega]-silyl hydride-functionalized polystyrene, alkoxysilyl-functionalized polystyrene was obtained in high yield (83 %). The main side product was vinylsilane-functionalized polymer. A small amount of dimer (approximately 2 %) was formed from the hydrosilation reaction of silyl hydride-functionalized polymer and vinylsilane-functionalized polymer. Star polymers with an average number of 6.8 arms were obtained by reacting poly(styryl)lithium with 6.6 equivalents of vinyldimethylchlorosilane in benzene at 30 °C. It was found that, in benzene at 30 °C, vinyldimethylchlorosilane is an efficient linking agent for the preparation of well-defined star-branched polymers. In contrast, the reaction of poly(styryl)lithium with 5 equivalents of vinyldimethylchlorosilane in THF at -78 °C produced vinylsilane-functionalized polymer in high yield (> 93 %). Poly(styryl)lithium was reacted with 2.5 equivalents of vinyldimethylethoxysilane; reaction occurred exclusively by the addition of the living anion to the vinyl group. In-chain, dihydroxyl-functionalized polystyrene was prepared by reaction of poly(styryl)lithium and 1,3-butadiene diepoxide. The hydroxyl functionalities were activated with potassium naphthalenide. Addition of ethylene oxide monomer yielded the corresponding heteroarm polystyrene/poly(ethylene oxide) stars. Two commercially available triepoxides, N,N-diglycidyl-4-glycidyloxyaniline and Tactix 742, were used to prepare the corresponding 3-armed stars in high yield.
Book Synopsis Polymer Yearbook by : Richard A. Pethrick
Download or read book Polymer Yearbook written by Richard A. Pethrick and published by CRC Press. This book was released on 1991 with total page 472 pages. Available in PDF, EPUB and Kindle. Book excerpt: This volume contains reviews on state-of-the-art Japanese research presented in the annual Spring and Autumn meetings of the Japanese Polymer Science Society. The aim of this section is to make information on the progress of Japanese Polymer Science, and on topics of current interest to polymer scientists in Japan, more easily available worldwide.
Book Synopsis Dissertation Abstracts International by :
Download or read book Dissertation Abstracts International written by and published by . This book was released on 2005 with total page 918 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis The Synthesis and Characterization of Well-defined Branched Polymeric Molecules with Anionic Polymerization by : Aubrey Brewer Gosnell
Download or read book The Synthesis and Characterization of Well-defined Branched Polymeric Molecules with Anionic Polymerization written by Aubrey Brewer Gosnell and published by . This book was released on 1967 with total page 342 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Synthesis of Polymers by : Dieter A. Schlüter
Download or read book Synthesis of Polymers written by Dieter A. Schlüter and published by John Wiley & Sons. This book was released on 2012-05-23 with total page 1229 pages. Available in PDF, EPUB and Kindle. Book excerpt: Polymers are huge macromolecules composed of repeating structural units. While polymer in popular usage suggests plastic, the term actually refers to a large class of natural and synthetic materials. Due to the extraordinary range of properties accessible, polymers have come to play an essential and ubiquitous role in everyday life - from plastics and elastomers on the one hand to natural biopolymers such as DNA and proteins on the other hand. The study of polymer science begins with understanding the methods in which these materials are synthesized. Polymer synthesis is a complex procedure and can take place in a variety of ways. This book brings together the "Who is who" of polymer science to give the readers an overview of the large field of polymer synthesis. It is a one-stop reference and a must-have for all Chemists, Polymer Chemists, Chemists in Industry, and Materials Scientists.
Book Synopsis Anionic Polymerization: Principles and Practice by : Maurice Morton
Download or read book Anionic Polymerization: Principles and Practice written by Maurice Morton and published by Elsevier. This book was released on 2012-12-02 with total page 257 pages. Available in PDF, EPUB and Kindle. Book excerpt: Anionic Polymerization: Principles and Practice describes the unique nature of the anionic mechanism of polymerization. This book is composed of two parts encompassing 11 chapters that cover the aspects of the synthetic possibilities inherent in this system. Part I deals with the various aspects of anionic polymerization mechanism, including the monomers, initiators, solvents, and the involved initiation and propagation reactions. This part also describes the copolymerization and organolithium polymerization reactions of styrene and dienes. Part II explores the applications of anionic polymerization in polymer synthesis. This part specifically tackles the synthesis of narrow molecular weight, branched and a,?-difunctional polymers, and block copolymers. Polymer chemists and researchers who work in the chemical industry and who would wish to utilize the unique features of anionic polymerization in the synthesis of new products will find this book invaluable.
Download or read book Maro Polymer Notes written by and published by . This book was released on 2000 with total page 280 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Controlled Synthesis and Characterization of Branched, Functionalized, and Cyclic Polymers by : Vijay Chavan
Download or read book Controlled Synthesis and Characterization of Branched, Functionalized, and Cyclic Polymers written by Vijay Chavan and published by . This book was released on 2011 with total page 212 pages. Available in PDF, EPUB and Kindle. Book excerpt: A variety of methods were used to make polymers with different architecture and functionalities. The linking chemistry of vinyldimethylchlorosilane (VDMCS) with poly(styryl)lithium (M[subscript n] = 1,700-3,000 g/mol) was studied. The average degree of branching varied from 7.5 to 9.4 with an increase in concentration of VDMCS (1.2 to 5.2 eq). The intrinsic viscosities and melt viscosities (at 160°C) of the star polymers were found to be less than half of that of the corresponding linear polystyrenes. [alpha]-Pyrrolidine-functionalized polystyrene (M[subscript n] = 2,700 g/mol, M[subscript w]/M[subscript n] = 1.03, 92.5%) was successfully synthesized from [alpha]-chloromethyldimethylsilane-functionalized polystyrene (M[subscript n] = 2,600 g/mol, M[subscript w]/M[subscript n] = 1.02) based on NMR spectroscopy, MALDI-TOF and ESI mass spectrometry. The stability of silyl hydride groups under atom transfer radical polymerization conditions was proven by copolymerizing methyl methacrylate and (4-vinylphenyl)dimethylsilane (VPDS). Tapered block copolymers of isoprene, VPDS, and styrene with narrow molecular weight distributions (1.04 and 1.05) were synthesized via anionic polymerization. Evidence regarding the topology of cyclic polybutadienes was obtained by Atomic Force Microscopy of grafted polymers obtained by grafting an excess of silyl hydride-functionalized polystyrene (M[subscript n] = 8,300 g/mol, M[subscript w]/M[subscript n] =1.01) onto cyclic polybutadiene (M[subscript n]=88,000 g/mol, M[subscript w]/M[subscript n] = 2.0). The reactivity of polyisobutylene carbocations was compared with respect to competitive electrophilic addition to a vinyl group versus silyl hydride transfer by investigating the reaction with VPDS. Based on GPC results, and 1H and 13C NMR spectroscopy, no evidence for any vinyl group addition was observed. A successful attempt was made to prepare electrospun fibers from fluoro-functionalized styrene-butadiene elastomers. The water contact angle of these surfaces was found to be 162.8° [plus or minus] 3.8° for the fibrous mat of the fluorinated polymers as compared to 151.2° [plus or minus] 2.4° for the analogous fibrous mat of the non-fluorinated polymers. In-chain functionalization of tapered styrene butadiene rubber using chloromethydimethylsilane was quantitatively done via a hydrosilation reaction. Pyrrolidine-functionalized styrene butadiene rubber was obtained in 71% yield after reacting pyrrolidine with chloromethyldimethylsilane-functionalized styrene butadiene rubber. In-chain, silyl hydride-functionalized, deuterated polystyrene (M[subscript n] = 2,100 g/mol, M[subscript w]/M[subscript n] = 1.01) was functionalized with allyl cyanide in the presence of Karstedt's catalyst to obtain in-chain cyano-functionalized, deuterated polystyrene (45% based on the mass of in-chain, cyano-functionalized deuterated polystyrene obtained).
Book Synopsis Recent Advances in Anionic Polymerization by : T.E. Hogen-Esch
Download or read book Recent Advances in Anionic Polymerization written by T.E. Hogen-Esch and published by Springer. This book was released on 1987-06-30 with total page 488 pages. Available in PDF, EPUB and Kindle. Book excerpt: Over the years the field of anionic polymerization has attracted numerous outstanding scientists, and today it still is being pursued by many researchers all over the world. The exciting discovery of termination-less polymerization processes and living polymers culminating in the development of narrow molecular weight polymers, star polymers, and tailor-made block and graft copolymers, contributed immensely to the rapid expansion of polymer science. Areas of active research in anionic polymerization presently include the structure of ion pairs and their role in regulating polymer structure, ring opening polymerization of heterocyclic monomers, synthesis of well-defined block and graft copolymers including the application of macromers in such systems, telechelic polymers with functional end groups, and other topics. New developments in the organic chemistry of carbanions such as dipolar carbanions impinge on the field of anionic polymerization. More sophisticated characterization techniques have been instrumental in obtaining better correlations between the structure of polymers and that of intermediates leading to their formation. This book contains the proceedings of the international symposium on "Recent Advances in Anionic Polymerization and Related Processes" which was held at the 1986 spring meeting of the American Chemical Society. It was the first Polymer Division-sponsored meeting exclusively devoted to anionic polymerization since the Houston ACS meeting in the spring of 1980. The proceedings of that meeting were published in the book "Anionic Polymerization", ACS Symposium Series No. 166, edited by Dr. J. E. McGrath.
Download or read book Polymer Yearbook written by and published by . This book was released on 1991 with total page 480 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis American Doctoral Dissertations by :
Download or read book American Doctoral Dissertations written by and published by . This book was released on 1988 with total page 728 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Synthesis of End-chain and In-chain Functionalized Polymers by Anionic Polymerization by : Michael Olechnowicz
Download or read book Synthesis of End-chain and In-chain Functionalized Polymers by Anionic Polymerization written by Michael Olechnowicz and published by . This book was released on 2008 with total page 196 pages. Available in PDF, EPUB and Kindle. Book excerpt: "The synthesis of homopolymers and block copolymers containing metal coordinating ligands is an important area of research due to the potential applications of these polymers in the fields of optics, electronics, and photonics. Specifically, the terpyridine group is very useful, since it can act as a tridentate chelating ligand due to its strategically positioned, three nitrogen atoms. This allows it to form strong complexes with a variety of transition metal ions. The hydroxyl functionality is another important group due to numerous applications of well-defined hydroxyl-functionalized polymers. They can react with other functional groups on other polymers for chain extension, branching, or crosslinking. They can also be used as macroinitiators for the polymerization of other monomers such as lactide and lactone. Alkyllithium-initiated, living anionic polymerization offers excellent control over molecular weight and molecular weight distribution. The absence of termination and chain transfer steps makes these systems ideally suited for the preparation of chain-end functionalized polymers by the reaction of the living chain ends with appropriate monomers or terminating agents. A recently reported general anionic functionalization method was used to create well-defined terpyridine and hydroxyl end-functionalized polymers. In the first step, living polymeric organolithium compounds were reacted with silyl chlorides to form the corresponding silyl hydride-functionalized polymers. Then, these polymers were reacted with substituted alkenes in the presence of a hydrosilation catalyst to form the corresponding functionalized polymers. A new method was also developed, based on similar chemistry, to prepare an in-chain functionalized diblock copolymer where a variety of functional groups can be placed directly at the interface of the two blocks. This method was used to prepare both in-chain hydroxyl- and terpyridine-functionalized polystyrene-b-polyisoprene copolymers. Lewis bases effect dramatic changes in microstructure, initiation rates, propagation rates and monomer reactivity ratios for alkyllithium-initiated polymerizations of vinyl monomers in hydrocarbon solution. The stability of polymeric organolithium compounds and the mechanism of decomposition in the presence of various stoichiometric equivalents of tetrahydrofuran in benzene solutions were studied due the importance of THF as an additive."--Abstract.
Book Synopsis Anionic Synthesis of Functionalized Polymers by : Jonathan E. Janoski
Download or read book Anionic Synthesis of Functionalized Polymers written by Jonathan E. Janoski and published by . This book was released on 2010 with total page 160 pages. Available in PDF, EPUB and Kindle. Book excerpt: The synthesis of well-defined functionalized polymers is an important area of research due to their wide array of applications. The work presented herein can be divided into three categories: a) functional initiator synthesis; b) chain-end and in-chain functionalization and c) functional monomer synthesis and polymerization. All three methods involve both anionic polymerization and hydrosilation. In this work, all anionic polymerizations were performed at room temperature in hydrocarbon solvent with an alkyllithium initiator. A functional 4-pentenyllithium initiator was prepared in 70% yield and was used for the synthesis of [alpha] and [alpha,omega]-functionalized polystyrene. 4-Pentenyllithium was used to initiate styrene polymerization in benzene in the presence of 5 equivalents of tetrahydrofuran. Narrow polydispersity indices and good agreement between calculated and observed molecular weights were observed for the methanol-terminated product. [alpha]-Triethoxysilyl-functionalized polystyrene was quantitatively prepared by hydrosilation with triethoxysilane and [alpha]-4-pentenylpolystyrene. [alpha]-4-Pentenyl-[omega]-silyl hydridefunctionalized polystyrene and [alpha]-4-pentenyl-[omega]-thiol hydride functionalized polystyrene were quantitatively prepared by terminating [alpha]-4-pentenylpoly(styryl)lithium with chlorodimethylsilane and ethylene sulfide, respectively. The [alpha]-4-pentenyl-[omega]-silyl hydride-functionalized polystyrene showed good agreement between calculated and observed molecular weights and a narrow polydispersity. [alpha]-4-Pentenyl-[omega]-thiolfunctionalized polystyrene showed a dimer peak due to oxidative coupling when quenched with methanol. Triethoxysilyl-functionalized, high-1,4-polybutadiene was prepared by reacting the pendant double bonds of the 1,2-units with triethoxysilane via hydrosilation. High-yielding reactions between the polymeric organolithium chain-ends and silyl chlorides were used to obtain the desired polymeric silyl hydrides for further functionalization. In-chain and chain-end cyano-functionalized polystyrenes were prepared. Chain-end, silyl hydride-functionalized polystyrene was prepared quantitatively. Hydrosilation of chain-end, silyl hydride-functionalized polystyrene with allyl cyanide resulted in [omega]-cyano-functionalized polystyrene, which was prepared in 87% yield. In-chain, silyl hydride-functionalized polystyrene was prepared by terminating excess poly(styryl)lithium with dichloromethylsilane. The remaining poly(styryl)lithium was terminated with ethylene oxide to aid in chromatographic separation to yield the pure in-chain, silyl hydride-functionalized polystyrene in 96% yield. Hydrosilation of in-chain, silyl hydride-functionalized polystyrene with allyl cyanide resulted in cyano in-chain functionalized polystyrene in 58% yield after 2 weeks of reaction time at elevated temperature. [omega]-Silyl dihydride-functionalized polystyrene was prepared in 92% yield by inverse addition of poly(styryl)lithium to dichloromethylsilane then reduction with lithium aluminum hydride. Functionalization with allyl cyanide yielded [omega]-dicyanofunctionalized polystyrene quantitatively. Synthesis of functionalized polymers from silyl hydride-substituted monomers was also investigated. para-Dimethylsilylstyrene was prepared from 4-chlorostyrene in 84% yield. Homopolymerization, copolymerization, and end-capping of poly(styryl)lithium in cyclohexane with this monomer was investigated, and it was found that a linking reaction is occuring. meta-Dimethylsilylstyrene was prepared from 3-bromostyrene in 75% yield. Anionic homopolymerization, and copolymerization of this monomer were investigated, and it was found that a more vigorous linking reaction was taking place compared to the para-substituted analog.
Book Synopsis Self-Healing Polymers by : Wolfgang H. Binder
Download or read book Self-Healing Polymers written by Wolfgang H. Binder and published by John Wiley & Sons. This book was released on 2013-03-29 with total page 638 pages. Available in PDF, EPUB and Kindle. Book excerpt: Self-healing is a well-known phenomenon in nature: a broken bone merges after some time and if skin is damaged, the wound will stop bleeding and heals again. This concept can be mimicked in order to create polymeric materials with the ability to regenerate after they have suffered degradation or wear. Already realized applications are used in aerospace engineering, and current research in this fascinating field shows how different self-healing mechanisms proven successful by nature can be adapted to produce even more versatile materials. The book combines the knowledge of an international panel of experts in the field and provides the reader with chemical and physical concepts for self-healing polymers, including aspects of biomimetic processes of healing in nature. It shows how to design self-healing polymers and explains the dynamics in these systems. Different self-healing concepts such as encapsulated systems and supramolecular systems are detailed. Chapters on analysis and friction detection in self-healing polymers and on applications round off the book.
Book Synopsis Complex Macromolecular Architectures by : Nikos Hadjichristidis
Download or read book Complex Macromolecular Architectures written by Nikos Hadjichristidis and published by John Wiley & Sons. This book was released on 2011-04-20 with total page 840 pages. Available in PDF, EPUB and Kindle. Book excerpt: The field of CMA (complex macromolecular architecture) stands at the cutting edge of materials science, and has been a locus of intense research activity in recent years. This book gives an extensive description of the synthesis, characterization, and self-assembly of recently-developed advanced architectural materials with a number of potential applications. The architectural polymers, including bio-conjugated hybrid polymers with poly(amino acid)s and gluco-polymers, star-branched and dendrimer-like hyperbranched polymers, cyclic polymers, dendrigraft polymers, rod-coil and helix-coil block copolymers, are introduced chapter by chapter in the book. In particular, the book also emphasizes the topic of synthetic breakthroughs by living/controlled polymerization since 2000. Furthermore, renowned authors contribute on special topics such as helical polyisocyanates, metallopolymers, stereospecific polymers, hydrogen-bonded supramolecular polymers, conjugated polymers, and polyrotaxanes, which have attracted considerable interest as novel polymer materials with potential future applications. In addition, recent advances in reactive blending achieved with well-defined end-functionalized polymers are discussed from an industrial point of view. Topics on polymer-based nanotechnologies, including self-assembled architectures and suprastructures, nano-structured materials and devices, nanofabrication, surface nanostructures, and their AFM imaging analysis of hetero-phased polymers are also included. Provides comprehensive coverage of recently developed advanced architectural materials Covers hot new areas such as: click chemistry; chain walking; polyhomologation; ADMET Edited by highly regarded scientists in the field Contains contributions from 26 leading experts from Europe, North America, and Asia Researchers in academia and industry specializing in polymer chemistry will find this book to be an ideal survey of the most recent advances in the area. The book is also suitable as supplementary reading for students enrolled in Polymer Synthetic Chemistry, Polymer Synthesis, Polymer Design, Advanced Polymer Chemistry, Soft Matter Science, and Materials Science courses. Color versions of selected figures can be found at www.wiley.com/go/hadjichristidis
Book Synopsis Synthesis of Well-defined Single and Multiphase Polymers Using Various Living Polymerization Methods by : Joseph M. DeSimone
Download or read book Synthesis of Well-defined Single and Multiphase Polymers Using Various Living Polymerization Methods written by Joseph M. DeSimone and published by . This book was released on 1990 with total page 660 pages. Available in PDF, EPUB and Kindle. Book excerpt:
