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"

1

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 temperatur
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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
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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
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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 ge
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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 cellu
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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
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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
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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 chromatograp
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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"

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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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