Relevant bibliographies by topics / Ring-opening polymerization of hexachlorocyclotriphosphazene

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Ring-opening polymerization of hexachlorocyclotriphosphazene'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Ring-opening polymerization of hexachlorocyclotriphosphazene"

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Yang, Ming Shan, Jian Wei Liu, Jin Yu, Xu Zhang, Jing Wei, and Lin Kai Li. "The Synthesis and Properties of a Novel Solid Polyphosphazene Electrolyte for Lithium Ion Battery." Advanced Materials Research 148-149 (October 2010): 749–52. http://dx.doi.org/10.4028/www.scientific.net/amr.148-149.749.

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Polydichlorophosphazene was synthesized from hexachlorocyclotriphosphazene by high-temperature ring-opening polymerization, and poly(2-(2-methoxyethoxy) ethanol phosphazene)(MEEP) was synthesized by reacting polydichlorophosphazene with alcohol sodium. The optimal synthesis parameters were obtained and the structure of MEEP was analyzed by NMR. Then polyphosphazene electrolyte was prepared by mixing MEEP with LiCF3SO3. The results indicated that the electrolyte prepared in this paper has high decomposition temperature, and its room-temperature conductivity is up to 1.187×10-4 S/cm.
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Borisov, Alexey S., Paul Hazendonk, and Paul G. Hayes. "31P MAS NMR Spectroscopy of Hexachlorocyclotriphosphazene at Different Stages During Thermal Ring-Opening Polymerization." Journal of Inorganic and Organometallic Polymers and Materials 20, no. 2 (2009): 395–98. http://dx.doi.org/10.1007/s10904-009-9316-2.

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Carolina Martínez Ceballos, Evelyn, Ricardo Vera Graziano, Gonzalo Martínez Barrera, and Oscar Olea Mejía. "Synthesis and Characterization of Polyphosphazenes Modified with Hydroxyethyl Methacrylate and Lactic Acid." International Journal of Polymer Science 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/645869.

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Poly(dichlorophosphazene) was prepared by melt ring-opening polymerization of the hexachlorocyclotriphosphazene. Poly[bis(2-hydroxyethyl-methacrylate)-phosphazene] and poly[(2-hydroxyethyl-methacrylate)-graft-poly(lactic-acid)-phosphazene] were obtained by nucleophilic condensation reactions at different concentrations of the substituents. The properties of the synthesized copolymers were assessed by FTIR,1H-NMR and31P-NMR, thermal analysis (DSC-TGA), and electron microscopy (SEM). The copolymers have a block structure and show twoTg's below room temperature. They are stable up to a temperature of 100°C. The type of the substituents attached to the PZ backbone determines the morphology of the polymers.
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Allcock, Harry R., David J. Brennan, and Robert W. Allen. "Reactions between hexachlorocyclotriphosphazene and hexamethylcyclotrisiloxane: polymerization, ring cleavage, and crosslinking." Macromolecules 18, no. 2 (1985): 139–44. http://dx.doi.org/10.1021/ma00144a004.

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Sennett, Michael S., Gary L. Hagnauer, Robert E. Singler, and Geoffrey Davies. "Kinetics and mechanism of the boron trichloride-catalyzed thermal ring-opening polymerization of hexachlorocyclotriphosphazene in 1,2,4-trichlorobenzene solution." Macromolecules 19, no. 4 (1986): 959–64. http://dx.doi.org/10.1021/ma00158a003.

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Ganapathiappan, S., K. S. Dhathathreyan, and S. S. Krishnamurthy. "New initiators for the ring-opening thermal polymerization of hexachlorocyclotriphosphazene: synthesis of linear poly(dichlorophosphazene) in high yields." Macromolecules 20, no. 7 (1987): 1501–5. http://dx.doi.org/10.1021/ma00173a010.

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Penczek, Stanislaw, Julia Pretula, and Stanislaw Slomkowski. "Ring-opening polymerization." Chemistry Teacher International 3, no. 2 (2021): 33–57. http://dx.doi.org/10.1515/cti-2020-0028.

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Abstract Ring-opening polymerization is defined by IUPAC (Penczek, S., Moad, G. (2008). Glossary of the terms related to kinetics, thermodynamics, and mechanisms of polymerization. (IUPAC Recommendations 2008), Pure and Applied Chemistry, 80(10), 2163–2193) as (cit.) “Ring-opening polymerization (ROP): Polymerization in which a cyclic monomer yields a monomeric unit that is either acyclic or contains fewer rings than the cyclic monomer”. The large part of the resulting polymerizations is living/controlled; practically all belong to chain polymerizations. After the introduction, providing basic information on chain polymerizations, the paper presents the concise overview of major classes of monomers used in ROP, including cyclic ethers, esters, carbonates, and siloxanes as well as cyclic nitrogen, phosphorus, and sulfur containing monomers. There are discussed also thermodynamics, kinetic polymerizability, and major mechanisms of ROP. Special attention is concentrated on polymers prepared by ROP on industrial scale.
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Cho, Iwhan, and Sang-Keun Kim. "Exploratory ring-opening polymerization: Ring-opening polymerization of vinylketene cyclic acetal." Journal of Polymer Science Part C: Polymer Letters 28, no. 13 (1990): 417–21. http://dx.doi.org/10.1002/pol.1990.140281304.

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Kamber, Nahrain E., Wonhee Jeong, Robert M. Waymouth, Russell C. Pratt, Bas G. G. Lohmeijer, and James L. Hedrick. "Organocatalytic Ring-Opening Polymerization." Chemical Reviews 107, no. 12 (2007): 5813–40. http://dx.doi.org/10.1021/cr068415b.

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Inoue, Shohei. "Coordination ring-opening polymerization." Progress in Polymer Science 13, no. 1 (1988): 63–81. http://dx.doi.org/10.1016/0079-6700(88)90011-1.

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Dissertations / Theses on the topic "Ring-opening polymerization of hexachlorocyclotriphosphazene"

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Heston, Amy Jeannette. "Lewis and Brönsted Acid Adducts of Hexachlorocyclotriphosphazene and Carboxylate Derivatives of Disilanes." University of Akron / OhioLINK, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=akron1123190192.

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Riat, D. P. S. "The ring opening polymerization of ring strained cyclic ethers." Thesis, Aston University, 1992. http://publications.aston.ac.uk/9785/.

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The kinetics and mechanisms of the ring-opening polymerization of oxetane were studied using cationic and coordinated anionic catalysts. The cationic initiators used were BF30Et2!/ethanol, BF30Et2!/ethanediol and BF30Et2/propantriol. Kinetic determinations with the BF30Et2/diol system indicated that a 1: 1 BF3:0H ratio gave the maximum rate of polymerization and this ratio was employed to detenmne the overall rates of polymerization. An overall second-order dependence was obtained when the system involved ethanediol or propantriol as co-catalyst and a 3/2-order dependence with ethanol, in each case the monomer gave a first-order relationship. This suggested that two mechanisms accounted for the cationic polymerization. These mechanisms were investigated and further evidence for these was obtained from the study of the complex formation of BF30Et2 and the co-catalysts by 1H NMR. Molecular weight studies (using size-exclusion chromatography) indicated that the hydroxyl ion acted as a chain transfer reagent when the [OH] > [BF3]. A linear relationship was observed when the number average molecular weight was plotted against [oxetane] at constant [BF3:0H], and similarly a linear dependency was observed on the BF3:0H 1:1 adduct at constant oxetane concentration. Copolymerization of oxetane and THF was carried out using BF30Et2/ethanol system. The reactivity ratios were calculated as rOXT = 1.2 ± 0.30 and rTHF = 0.14 ± 0.03. These copolymers were random copolymers with no evidence of oligomer formation. The coordinated anionic catalyst, porphinato-aluminium chloride [(TPP)AICl], was used to produce a living polymerization of oxetane. An overall third-order kinetics was obtained, with a second-order with respect to the [(TPP)AICl] and a first-order with respect to the [oxetane] and a mechanism was postulated using these results. The stereochemistry of [(TPP)AlCl] catalyst was investigated using cyclohexene and cyclopentene oxide monomers, using extensive 1H NMR, 2-D COSY and decoupling NMR techniques it was concluded that [(TPP)AlCl] gave rise to stereoregular polymers.
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Mamleeva, Emiliya. "Amino- and imino-supported zinc complexes and their influence on ring opening polymerization and immortal ring opening polymerization of lactide." Thesis, University of British Columbia, 2015. http://hdl.handle.net/2429/54577.

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The alkoxy zinc complexes (±)-[(NNHOt-Bu)Zn(OCH₂Ph)]₂ 4, (±)-[(NNOt-Bu)Zn(OCH₂Ph)]₂ 5, and 6 (±)-[(NNOCm)Zn(OCH₂Ph)]₂ were prepared from the reactions of the corresponding alkyl zinc complexes (±)-(NNHOt-Bu)Zn(CH₂CH₃) 1, (±)-(NNOt-Bu)Zn(CH₂CH₃) 2, and (±)-(NNOCm)Zn(CH₂CH₃) 3, respectively, with benzyl alcohol (PhCH₂OH). All zinc compounds 1-6 were characterized by ¹H and ¹³C{¹H} NMR spectroscopy. The molecular structures of 2-6 were characterized by single-crystal X-ray crystallography. The alkyl zinc complexes are mononuclear with a tridentate coordination mode and a distorted tetrahedral geometry around the zinc metal centers. The alkoxy zinc catalysts show a dimeric feature containing two zinc metal centers bridging through the benzyl alkoxy oxygen atoms with different coordination modes for all three catalysts. The solution denticities of 4-6 were further investigated through 1D and 2D NMR spectroscopy experiments. Exchange studies with pyridine and complexes 4-6 were also conducted. The catalytic activities of alkyl and alkoxy zinc complexes 1-6 toward ring opening polymerization (ROP) of racemic lactide (rac-LA) have been studied by ¹H NMR spectroscopy, Gel permeation chromatography, and MALDI-TOF mass spectrometry. Experimental results indicate that the alkyl zinc compounds 1-3 show relatively less activity toward ROP of cyclic esters than the alkoxy zinc compounds 4-6. Catalysts 5 and 6 demonstrate a better control over experimental molecular weights and dispersity values of PLA, and more stereoselective than 4. Catalyst 4 undergoes the depolymerization reactions. Different transesterification side reactions operate at low equivalency polymerization studies to a different extent for all alkoxy zinc complexes. Immortal ROP of alkyl zinc compounds 1-3 was investigated in the presence of a chain transfer agent. The obtained results reveal the controlled nature of iROP.<br>Science, Faculty of<br>Chemistry, Department of<br>Graduate
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Lönnberg, Hanna. "Ring-opening polymerization from cellulose for biocomposite applications." Doctoral thesis, KTH, Ytbehandlingsteknik, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-10455.

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There is an emerging interest in the development of sustainable materials with high performance. Cellulose is promising in this regard as it is a renewablere source with high specific properties, which can be utilized as strong reinforcements in novel biocomposites. However, to fully exploit the potential ofcellulose, its inherent hydrophilic character has to be modified in order toimprove the compatibility and interfacial adhesion with the more hydrophobicpolymer matrices commonly used in composites.In this study, the grafting of poly(ε-caprolactone) (PCL) and poly(L-lactide)(PLLA) from cellulose surfaces, via ring-opening polymerization (ROP) of ε-caprolactone and L-lactide, was investigated. Both macroscopic and nano-sizedcellulose were explored, such as filter paper, microfibrillated cellulose (MFC),MFC-films, and regenerated cellulose spheres. It was found that thehydrophobicity of the cellulose surfaces increased with longer graft lengths, andthat polymer grafting rendered a smoother surface morphology.To improve the grafting efficiency in the ROP from filter paper, both covalent(bis(methylol)propionic acid, bis-MPA) and physical pretreatment (xyloglucanbisMPA)were explored. The highest grafting efficiency was obtained with ROPfrom the bis-MPA modified filter papers, which significantly increased amountof polymer on the surface, i.e. the thickness of the grafted polymer layer.MFC was grafted with PCL to different molecular weights. The dispersability innon-polar solvent was obviously improved for the PCL grafted MFC, incomparison to neat MFC, and the stability of the MFC suspensions was better maintained with longer grafts. PCL based biocomposites were prepared from neat MFC and PCL grafted MFCwith different graft lengths. The polymer grafting improved the mechanical properties of the composites, and the best reinforcing effect was obtained when PCL grafted MFC with the longest grafts were used as reinforcement.A bilayer laminate consisting of PCL and MFC-films grafted with different PCL graft lengths displayed a gradual increase in the interfacial adhesion with increasing graft length.The effect of grafting on the adhesion was also investigated via colloidal probeatomic force microscopy at different temperatures and time in contact. A significant improvement in the adhesion was observed after polymer grafting.<br>QC 20100730
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Hastings, Jedidiah M. "Olefin metathesis in supramolecular and ring-opening polymerization." [Gainesville, Fla.] : University of Florida, 2006. http://purl.fcla.edu/fcla/etd/UFE0015602.

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Milligan, Brian David. "Studies on ring-opening polymerization by metathesis catalysts." Thesis, Queen's University Belfast, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317083.

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Neqal, Mehdi. "Smart polymeric materials by ring-opening metathesis polymerization." Thesis, Bordeaux, 2017. http://www.theses.fr/2017BORD0658/document.

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Ce travail de thèse consiste à combattre le développement microbien des réservoirs de carburant aéronautiques dont le métabolisme entraine la production d’acides organiques susceptibles de corroder les parois métalliques des réservoirs. Des substances biocides sont habituellement utilisées pour éliminer les populations microbiennes. Ces substances peuvent être des composés organiques ou bien de manière plus courante du chrome (VI) sous forme de revêtement à la surface des parois afin de créer une couche passive et d’empêcher la corrosion chimique. Cependant, le chrome appartient à la catégorie des substances cancérogènes, mutagènes et reprotoxiques et se trouve maintenant soumis à restriction par la réglementation européenne Registration, Evaluation and Authorization of Chemicals (REACh). Pour remplacer les systèmes en place, le choix s’est porté sur la préparation de particules polymères pH-sensibles capables de libérer une molécule biocide en présence de microorganismes. De telles particules sont obtenues par copolymérisation par métathèse de cyclo-oléfines (ROMP) de norbornène avec un macromonomère linéaire de polyglycidol α-norbornenyl. Ce dernier permet d’une part la stabilisation des particules et d’autre part la multifonctionnalisation de l’objet par des molécules de biocide. Celles-ci sont introduites sur la chaîne de polyglycidol via un lien imine pH-sensible par substitution des fonctions hydroxyle par des entités dodécylamine. La libération du biocide à un pH inférieur à 7 a été validée ainsi que les capacités de ces particules à lutter contre des microorganismes tel que Hormoconis resinae souche identifiée comme se développant dans les réservoirs d’avions. Dans une dernière étape, les particules fonctionnalisées dodécylamine ont été incorporées dans un revêtement usuel en aéronautique et la capacité des particules à ne pas altérer la résistance du revêtement de base à des conditions de corrosion extrêmes a permis de vérifier leur applicabilité dans ce domaine<br>The aim of this Thesis work was to address the issue of microbial contamination inside fuel tanks. Microorganisms induce the chemical corrosion of airplane tank walls due to their production of organic acids. Biocide compounds are typically used to inhibit these microorganisms, either in the form of organic small molecules, or most commonly as chromium-based coatings on the walls to hinder chemical corrosion. Organic biocides need to be replenished regularly, while chromium is a particularly dangerous compound targeted by the European Registration, Evaluation and Authorization of Chemicals (REACh) legislation due to its carcinogenic nature. A replacement approach selected for this project was the development of a smart system of multifunctional polymeric particles synthesized by dispersion ROMP, which can deliver a biocide following an acidic trigger due to the presence of microorganisms. The polymerization utilized a linear α-norbornenyl-polyglycidol macromonomer as a reactive surfactant. The hydroxyl-rich polyglycidol backbone of the macromonomer was beneficial for the conjugation of dodecylamine through a pH-sensitive imine bond and permitted the preparation of highly functionalized bioactive particles. A proof of concept for the pH sensitivity of the system was provided and the antifungal efficacy of the biocide-functionalized macromonomer and particles was verified. The particles were also integrated in a coating formulation to simulate their application on tank walls. The qualities of the original coating were preserved even after prolonged exposure to corrosive conditions, making this system viable for its foreseen application
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Chen, Mingfei III. "Macrocyclic Monomers: Synthesis, Characterization and Ring-opening Polymerization." Diss., Virginia Tech, 1997. http://hdl.handle.net/10919/30720.

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Interest in macrocyclic monomers can be dated back to the 1960's. The recent surge of research activities in this area is prompted by two facts: the encouraging discovery of high yield synthesis and facile ring-opening polymerization of cyclic polycarbonate; the need for a technique to solve the tough processibility problem of high performance polymers. This work was intended to address the following aspects in the cyclic poly(ether ketone) or sulfone system. The first goal was to understand the structure-property relationship of this type of macrocycles. A large number of macrocycles were synthesized by nucleophilic aromatic substitution cyclization reactions under pseudo-high dilution conditions. Pure individual macrocycles as well as cyclic mixtures were characterized by NMR, HPLC, GPC, FABMS, MALDI-TOF-MS, DSC and TGA. Comparison study suggests that the cyclic distribution is kinetically controlled. Several factors determine the melting points of individual macrocycles. The first factor is the ring size. A series of cyclic monomers for poly(ether ether ketone)s were synthesized and isolated. The melting point decreases as ring size increases. Single crystal X-ray structural results suggest that this phenomenon is related to the increased flexibility of the larger sized macrocycles. The second factor is the functional groups of the macrocycles. X-ray structural and GPC experiments reveal that the sulfone group is more rigid than the ketone group, than ether group. The effect of functional groups on melting point is in the order sulfone>ketone>ether. A third factor is the symmetry of the macrocycles. Breaking the symmetry of macrocycle through comacrocyclization dramatically decreases the melting point of individual macrocycles as well as the cyclic mixture as a whole. Based on these findings, a novel two step method was developed to control the ring size distribution, which effectively reduced the amount of the small sized macrocycle and decreased the melting point. In addition to the nucleophilic aromatic substitution cyclization, it was also demonstrated in this work that macrocycles can be synthesized by Friedel-Crafts acylation cyclization. However, this method is limited by the solubility problem. The ring-opening polymerization of macrocyclic monomers was systematically studied. Several factors were considered in this study: the nature and amount of catalyst, temperature and time. CsF; metallic phenolate and Na2S are good initiators. Conversion to near 100 % is possible under the controlled polymerization conditions. It was found that crosslinking is an inherent phenomenon. The molecular weight of the soluble fraction near complete conversion is almost independent of initiator and polymerization temperature. It is limited by the crosslinking reaction. It is demonstrated for the first time that the macrocyclic monomer techniques can be applied to more valuable semicrystalline systems. Tough polymers such as high performance poly(ether ether ketone)s were produced through ring-opening polymerization. The last chapter is devoted to the challenging synthesis of monodisperse poly(ether ether ketone)s. A convergent strategy was devised. A monofluoroaryl compound was synthesized by Friedel-crafts acylation reaction. The final monodisperse linear oligomers were generated by reacting the monofunctional compound with a bisphenol through a quantitative reaction.<br>Ph. D.
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Gouardères, Frédéric P. "The cationic ring-opening polymerization of cyclic ethers." Thesis, Aston University, 1995. http://publications.aston.ac.uk/9681/.

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The kinetics and mechanisms of ring opening polymerization and copolymerizntion of different cyclic ethers were studied using mainly a cationic system of iinitiation. BF30Et2/ethanediol. The cyclic ethers reacted differently showing that ring strain and basicity are the main driving forces in cationic ring opening polymerizaion. In most cases it was found that the degree of polymerization is controlled kinetically via terminations with the counterion and the monomers, and that the contribution of each type of reaction to the overall termination differs markedly. The Gel permeation chromatography studies showed that the molecular weight distribution of the samples of polyoxetanes were bimodal. This was in accordance with previous work establishing that the cyclic tetramer is found in much higher proportions than any of the other cyclic oligomers. However the molecular weight distribution of the copolymers made from oxetane and THF or from oxetane and oxepane were shown to be unimodal. These observations could be explained by a change in the structure of the growing end involved in the cationic polymerization. In addition crown ethers like dibenzo-crown-6 and compounds such as veratrole are believed to stabilise the propagating end and promote the formation of living polymers from oxetane.
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Stridsberg, Kajsa. "Controlled ring-opening polymerization : Polymers with designed macromolecular architechture." Doctoral thesis, KTH, Polymer Technology, 2000. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-2927.

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Books on the topic "Ring-opening polymerization of hexachlorocyclotriphosphazene"

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McGrath, James E., ed. Ring-Opening Polymerization. American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1985-0286.

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Penczek, S., P. Kubisa, and K. Matyjaszewski, eds. Cationic Ring-Opening Polymerization. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/3-540-13781-5.

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Handbook of ring-opening polymerization. Wiley-VCH, 2009.

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res, Fre de ric Pierre Gouarde. The cationic ring-opening polymerization of cyclic ethers. Aston University. Department of Chemical Engineering and Applied Chemistry, 1995.

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International Symposium on Ring-Opening Polymerization (1986 Blois, France). Ring opening polymerization: Lectures presented at the "IUPAC Fifth International Symposium on Ring-Opening Polymerization" in Blois, France, June 1986. Edited by Sigwalt P, Spassky N, Sekiguchi H, and International Union of Pure and Applied Chemistry. Hüthig & Wepf, 1987.

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Drăguțan, Valerian. Catalytic polymerization of cycloolefins: Ionic, Ziegler-Natta and ring-opening metathesis polymerization. Elsevier Science, 2000.

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T, Balaban Alexandru, and Dimonie M, eds. Olefin metathesis and ring-opening polymerization of cyclo-olefins. 2nd ed. Editura Academiei, 1985.

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Drăguțan, Valerian. Olefin metathesis and ring-opening polymerization of cyclo-olefins. 2nd ed. Editura Academiei, 1985.

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E, Khosravi, and Szymańska-Buzar T, eds. Ring opening metathesis polymerisation and related chemistry: State of the art and visions for the new century. Kluwer Academic Publishers, 2002.

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Naka, Kensuke. Ion, haii, kaikan, chikuji jūgō. Kyōritsu Shuppan, 2013.

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Book chapters on the topic "Ring-opening polymerization of hexachlorocyclotriphosphazene"

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Su, Wei-Fang. "Ring-Opening Polymerization." In Lecture Notes in Chemistry. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-38730-2_11.

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Koltzenburg, Sebastian, Michael Maskos, and Oskar Nuyken. "Ring-Opening Polymerization." In Polymer Chemistry. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49279-6_12.

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Gooch, Jan W. "Ring-Opening Polymerization." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_10069.

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Takasu, Akinori, and Terunari Hayashi. "Cationic Ring-Opening Polymerization." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29648-2_176.

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McGRATH, JAMES E. "Ring-Opening Polymerization: Introduction." In ACS Symposium Series. American Chemical Society, 1985. http://dx.doi.org/10.1021/bk-1985-0286.ch001.

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Sudo, Atsushi. "Anionic Ring-Opening Polymerization." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29648-2_172.

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Kobayashi, Shingo. "Ring-Opening Metathesis Polymerization." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29648-2_200.

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Inoue, Shohei, and Takuzo Aida. "Anionic Ring-Opening Polymerization." In New Methods for Polymer Synthesis. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-2356-1_2.

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Goethals, Eric J., and Ronny R. De Clercq. "Cationic Ring-Opening Polymerization." In New Methods for Polymer Synthesis. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4899-2356-1_3.

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Sudo, Atsushi. "Anionic Ring-Opening Polymerization." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-36199-9_172-1.

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Conference papers on the topic "Ring-opening polymerization of hexachlorocyclotriphosphazene"

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Pholharn, Dutchanee, Yottha Srithep, and John Morris. "Ring opening polymerization of poly(L-lactide) by macroinitiator." In MATERIALS CHARACTERIZATION USING X-RAYS AND RELATED TECHNIQUES. Author(s), 2019. http://dx.doi.org/10.1063/1.5088274.

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Liu, Ting, Shi-Jian Chen, and Bo-Quan Jiang. "Preparation of Methylphenylvinyl Raw Rubber by Bulk Polymerization and Ring-Opening Polymerization Methods." In 2015 International Conference on Material Science and Applications (icmsa-15). Atlantis Press, 2015. http://dx.doi.org/10.2991/icmsa-15.2015.61.

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Afsi, Nawel, Sami Othman, Toufik Bakir, Liborio I. Costa, Anis Sakly, and Nida Sheibat-Othman. "Dynamic optimization of a continuous Lactide ring-opening polymerization process." In 2019 International Conference on Control, Automation and Diagnosis (ICCAD). IEEE, 2019. http://dx.doi.org/10.1109/iccad46983.2019.9037934.

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Dirk, Shawn M., Patricia S. Sawyer, Jill Wheeler, Mark Stavig, and Bruce Tuttle. "High temperature polymer dielectrics from the ring opening metathesis polymerization (ROMP)." In 2009 IEEE Pulsed Power Conference (PPC). IEEE, 2009. http://dx.doi.org/10.1109/ppc.2009.5386251.

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Paraschis, Loukas, Yasuyuki Sugiyama, Annapoorna Akella, Tokuyuki Honda, and Lambertus Hesselink. "Properties of compositional volume grating formation with photoinitiated cationic-ring-opening polymerization." In SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, edited by Pericles A. Mitkas and Zameer U. Hasan. SPIE, 1998. http://dx.doi.org/10.1117/12.330437.

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Ling, Huaxu, Xiaoxiang Yu, Shifan Wang, Xiaohui Wang, and Liming Dong. "Study on ultrasonic assisted mechanism of ring opening polymerization of octamethylcyclotetrasiloxane (D4)." In MATERIALS SCIENCE, ENERGY TECHNOLOGY AND POWER ENGINEERING II (MEP2018). Author(s), 2018. http://dx.doi.org/10.1063/1.5041098.

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Kulig, Joseph B., Collin G. Moore, William J. Brittain, Sandra Gilmour, and Joseph W. Perry. "Synthesis of NLO polycarbonates via the ring-opening polymerization of macrocyclic prepolymers." In OE/LASE '94, edited by Seth R. Marder and Joseph W. Perry. SPIE, 1994. http://dx.doi.org/10.1117/12.173809.

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Liu, Peng, Jian-Bo Wu, Ge-Sheng Yang, and Hui-Li Shao. "KINETICS OF RING-OPENING POLYMERIZATION OF L-LACTIDE BY USING A TWIN-SCREW EXTRUDER." In 2015 International Conference on Material Engineering and Mechanical Engineering (MEME2015). WORLD SCIENTIFIC, 2016. http://dx.doi.org/10.1142/9789814759687_0059.

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Liu, Peng, Ge-Sheng Yang, Hui-Li Shao, and Xue-Chao Hu. "Kinetics of Ring-Opening Polymerization of L-lactide by Using a Tubular Static Mixing Reactor." In 2016 4th International Conference on Machinery, Materials and Computing Technology. Atlantis Press, 2016. http://dx.doi.org/10.2991/icmmct-16.2016.148.

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Kwasek, Beata, and Dariusz Bogdał. "Ring Opening Metathesis Polymerization of 7-Oxabicyclo[2.2.1]Hept-5-Ene-2,3- Dicarboxylic Acid, Dimethyl Ester." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-d009.

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Reports on the topic "Ring-opening polymerization of hexachlorocyclotriphosphazene"

1

Schrock, Richard R. Ring Opening Metathesis Polymerization. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada244693.

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Schrock, Richard S., Steven A. Krouse, Konrad Knoll, Jerald Feldman, John S. Murdzek, and Dominic C. Yang. Controlled Ring-Opening Metathesis Polymerization by Molybdenum and Tungsten Alkylidene Complexes. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada198073.

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Lambeth, Robert H., Joseph M. Dougherty, Joshua A. Orlicki, et al. Synthesis and Purification of Tunable High Tg Electro-Optical Polymers by Ring Opening Metathesis Polymerization. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada549234.

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Wallace, Kevin C., Andy H. Liu, John C. Dewan, and Richard R. Schrock. Preparation and Reactions of Tantalum Alkylidene Complexes Containing Bulky Phenoxide or Thiolate Ligands. Controlling Ring-Opening Metathesis Polymerization Activity and Mechanism Through Choice of Anionic Ligand. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada198293.

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Bazan, G. C., E. Khosravi, R. R. Schrock, W. J. Feast, and V. C. Gibson. Living Ring-Opening Metathesis Polymerization of 2,3-Difunctionalized- Norbornadienes by Mo(CH-t-Bu)(N-2,6-C(6)H(3)-i-Pr(2)(O-t-Bu)(2). Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada225986.

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Komiya, Zen, Coleen Pugh, and Richard R. Schrock. Synthesis of Side Chain Liquid Crystal Polymers by Living Ring Opening Metathesis Polymerization. 1. Influence of Molecular Weight, Polydispersity, and Flexible Spacer Length (n=2-8) on the Thermotropic behavior of the Resulting Polymers. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada248699.

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Zhou, Steven Q., Young T. Park, Georges Manuel, and William P. Weber. Composite Materials with Improved Properties in Compression. Appendix 2. Anionic Ring Opening Polymerization of 1-Silacyclopent-3-ene. Characterization of Poly(1-sila-cis-pent-3-ene) by 1H, 13C, and 29Si NMR Spectroscopy. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada221647.

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