Relevant bibliographies by topics / Norbornen

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

Academic literature on the topic 'Norbornen'

Author: Grafiati
Published: 4 June 2021
Last updated: 14 February 2022

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Journal articles on the topic "Norbornen"

1

Pock, Rudolf, Herbert Klein, and Herbert Mayr. "Elektrophile Alkylierungen von Norbornen – Synthese 7-substituierter Norbornene." Chemische Berichte 119, no. 3 (March 1986): 929–42. http://dx.doi.org/10.1002/cber.19861190316.

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Huang, Jianhui, Caifeng Li, Liu Liu, and Xuegang Fu. "Norbornene in Organic Synthesis." Synthesis 50, no. 15 (June 25, 2018): 2799–823. http://dx.doi.org/10.1055/s-0037-1610143.

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The norbornene skeleton possesses an alkene functionality with a fixed conformation, and represents unique reactivity. The use of norbornene and analogues as substrates is overviewed; reactivities are discussed as well as the role of norbornenes as ligands assisting modern organic transformations.1 Introduction2 Synthesis of Substituted Norbornenes2.1 Preparation of Functionalized Norbornenes by Deprotonation and Substitution Reactions2.2 Preparation of Functionalized Norbornenes under Palladium-Catalyzed­ Reaction Conditions2.3 Alkylation of Norbornene2.4 Multistep Synthesis3 Synthesis of Substituted Norbornanes3.1 Three-Membered-Ring Formation3.2 Formation of Four-Membered Rings3.3 Five- and Six-Membered Ring Formation3.4 Syntheses of Difunctionalized Norbornanes4 Synthesis of Cyclopentanes4.1 Oxidation Reactions4.2 Ring-Opening Cross Metathesis (ROCM)4.3 Ring-Opening Metathesis Polymerization (ROMP)4.4 Palladium-Catalyzed Ring-Opening of Norbornene5 Norbornene-Mediated Reactions5.1 Palladium Insertion into Carbon–Halide Bonds5.2 Palladium Insertion into N–H and C–H Bonds5.3 Norbornene as Ligand in Mediated Reactions6 Conclusion
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Della, Ernest W., and Wit K. Janowski. "Competing Radical- and Anion-Mediated Pathways in the Reduction of Bridgehead Tosylates with Lithium Aluminium Hydride." Australian Journal of Chemistry 52, no. 5 (1999): 367. http://dx.doi.org/10.1071/ch98165.

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Reaction of norborn-1-yl tosylate with lithium aluminium hydride in boiling tetrahydrofuran affords a mixture of norbornan-1-ol accompanied by the ring-opened products 4-methylcyclohexanol and 3-ethylcyclopentanol as their cis/trans isomers, as well as p-thiocresol and p-tolyl disulfide. Evidence strongly suggests that the reaction is mediated by the norborn-1-yloxy radical rather than the norborn-1-yloxy anion. The process is initiated by very slow acyl oxygen fission of the norbornyl tosylate, followed by reduction of the derived p-toluenesulfinate ion to give the p-thiocresoxide anion. Transfer of an electron from the latter to the substrate and decomposition of the derived norborn-1-yl tosylate radical anion leads to the norborn-1-yloxy radical which, upon ring opening, generates the monocyclic alcohols via the corresponding ketones. It is noteworthy that, when norborn-1-yl mesylate is exposed to lithium aluminium hydride, it yields norbornan-1-ol exclusively. In the absence of an efficient electron-transfer agent, the mechanism of reaction of norborn-1-yl mesylate is suggested to involve acyl oxygen fission only.
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Ding, Lin, Hailong Cheng, Yanqing Li, Ryo Tanaka, Takeshi Shiono, and Zhengguo Cai. "Efficient ethylene copolymerization with polar monomers using palladium anilinonaphthoquinone catalysts." Polymer Chemistry 9, no. 45 (2018): 5476–82. http://dx.doi.org/10.1039/c8py01292j.

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Moss, Robert A., and Xiaolin Fu. "Unexpected interconnection of the 7-norbornenyl and 3-nortricyclcyl/5-norbornen-2-yl cations." Tetrahedron Letters 45, no. 27 (June 2004): 5321–24. http://dx.doi.org/10.1016/j.tetlet.2004.04.134.

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Ermer, Otto, Peter Bell, and Sax A. Mason. "Doppelbindungsgeometrie von Norbornen: Neutronenbeugungsmessung eines Derivats bei 15 K." Angewandte Chemie 101, no. 9 (September 1989): 1298–301. http://dx.doi.org/10.1002/ange.19891010939.

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Thorn-Csányi, Emma, and Christian Harder. "RINGÖFFNENDE METATHETISCHE POLYMERISATION (ROMP) VON 5-CYANO-2-NORBORNEN." Angewandte Makromolekulare Chemie 185, no. 1 (February 1991): 283–92. http://dx.doi.org/10.1002/apmc.1991.051850127.

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Mitsudo, Take-Aki, Hiroshi Naruse, Teruyuki Kondo, Yoshihiko Ozaki, and Yoshihisa Watanabe. "Rutheniumkomplex-katalysierte [2 + 2]-Cycloaddition von Norbornen- mit Ethinderivaten." Angewandte Chemie 106, no. 5 (March 3, 1994): 595–97. http://dx.doi.org/10.1002/ange.19941060517.

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Sankara Subraranian, Rajaram, and Kalpattu Kuppusamy Balasubramanian. "Investigations on Mitsunobu reaction of 5-norbornen-2-ols." Tetrahedron Letters 31, no. 15 (January 1990): 2201–4. http://dx.doi.org/10.1016/0040-4039(90)80108-x.

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Eichinger, PCH, JH Bowie, and RN Hayes. "Stable Negative-Ion Isomers in the Gas Phase. C7H7O- Species." Australian Journal of Chemistry 42, no. 6 (1989): 865. http://dx.doi.org/10.1071/ch9890865.

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The C7H7O- ions formed by deprotonation of benzyl alcohol, norbornadien-7-ol and quadricyclin-7-ol are discrete species which all fragment by competitive losses of H, H2, CH2O and C6H6 on collisional activation. The isomeric ion from norbornen-2-one behaves differently undergoing retro cleavage to form HC2O- and C5H5- as product ions. The three deprotonated cresols are also distinct species. Anisole is deprotonated (by amide ion) to form both PhOCH2- and (C6H4)-OMe, ions which equilibrate prior to elimination of formaldehyde.
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Dissertations / Theses on the topic "Norbornen"

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Lassahn, Paul-Gerhard. "Neue Katalysatorsysteme für die Vinyl-Polymerisation von Norbornen." [S.l. : s.n.], 2003. http://www.freidok.uni-freiburg.de/volltexte/711.

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Gosmann, Mattis. "Norbornenhomo- und Copolymerisation durch Katalysatoren auf Basis der späten Übergangsmetalle." [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=960263012.

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Kirsten, André. "Chemisches Recycling von PVC-haltigen gemischten Polyolefinabfällen sowie COC-Materialien durch Pyrolyse und Optimierung von Versuchsparametern mittels Pyrolyse-GC-MS." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=96907364X.

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Tran, Phu-Dennis. "Ethen-Norbornen-Copolymerisation durch Single-site-Katalysatoren-MAO." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=968875459.

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Donner, Matthias. "Synthese und Pyrolyse von metallocen-katalysierten Ethen-Norbornen-Copolymeren." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=980197465.

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Müller, Julia Maria. "Metatheseabbau von Butadien-Acrylnitril-Copolymeren und neue Pfropfcopolymere aus Norbornen-terminierten Poly(ferrocenyldimethylsilan)en." kostenfrei, 2008. http://mediatum2.ub.tum.de/doc/646547/646547.pdf.

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Stöhr, Torsten. "Oberflächenmodifizierungen von Siliciumoxid und Poly(ethylen-stat-norbornen) durch Blockcopolymere und an Plasmaschichten gebundene Homopolymere." [S.l. : s.n.], 2000. http://ArchiMeD.uni-mainz.de/pub/2000/0107/diss.pdf.

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Júnior, Valdemiro Pereira de Carvalho. "Reatividade de complexos do tipo [RuCl2(S-dmso)2(NIII)2 para ROMP de norborneno." Universidade de São Paulo, 2008. http://www.teses.usp.br/teses/disponiveis/75/75132/tde-20062008-165939/.

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Este trabalho reporta sínteses e caracterizações de complexos do tipo [RuCl2(S-dmso)2(N)III)2], onde NIII = piridina, isonicotinamida e nicotinamida. Os complexos foram aplicados em ROMP de norborneno de modo investigar os efeitos cooperativos entre os ligantes ancilares dmso e aminasneste tipo de reação. O complexo com nicotinamida apresentou a maior atividade catalítica em 60 min a 50 ºC (20% de rendimento; Mw / Mn = 1,98). Os outros complexos derivados foram praticamente inertes para ROMP. Usando uma solução envelhecida por 140 min a 50 ºC do complexo com isonicotinamida, não foi observada mudanças significativas na atividade catalítica por 60 min a 50 ºC (17% de rendimento; Mw / Mn = 4,24). Experimentos com uma solução do complexo com isonicotinamida na presença do sal NBu4ClO4, o rendimento foi de 19% (Mw / Mn = 1,78) mediante as mesmas condições. Usando soluções irradiadas com luz branca (5-10 min) à temperatura ambiente, os complexos com piridina e isonicotinamida mostraram rendimentos de 36% (Mw / Mn = 1,8) e 26% (Mw / Mn = 1,7) por 60 min a 50 ºC, respectivamente. O complexo [RuCl3 (Ph2SO) 3] foi também isolado e sua atividade em ROMP para norborneno foi de 33% (Mw / Mn = 1,32) à temperatura ambiente por 5 min. O rendimento aumentou para 58% (Mw / Mn = 1,41) a 50 ºC por 30 min. Na presença do sal NBu4ClO4, o rendimento de reação não apresentou mudanças significativas. Dos resultados obtidos, conclui-se que os ligantes dmso e as aminas estudadas podem ser empregados como ligantes ancilares em complexos de Ru(II) para as reações de ROMP, considerando um efeito cooperativo de sintonia eletrônica.
This work reports the synthesis and characterizations of [RuCl2(S-dmso)2(N)III)2] complexes, where NIII = pyridine, isonicotinamide and nicotinamide. The complexes were applied in ROMP of norbornene in order to investigate the cooperative effects among the dmso and amines as ancillary ligands in this kind of reaction. The complex with nicotinamide showed the highest catalytic activity for 60 min at 50 ºC (20% yield; Mw / Mn = 1,98). The other derivatives were roughing inert for ROMP. Using an aged solution for 140 min at 50 ºC of the isonicotinamide complex, it was observed a significant change in their catalytic activity for 60 min at 50 ºC (17% yield; Mw / Mn = 4,24). Experiments using isonicotinamide complex solution in presence of the salt NBu4ClO4, the yield was 19% (Mw / Mn = 1,78) under similar conditions. When using irradiated solution with white lamp (5-10 min) at room temperature, the pyridine (for 10 min) and isonicotinamide (for 5 min) complexes showed yields of 36% (Mw / Mn = 1,8) and 26% (Mw / Mn = 1,7) for 60 min at 50 ºC respectively. The complex [RuCl3 (Ph2SO) 3] was also isolated and the ROMP active for norbornene was 33% (Mw / Mn = 1,32) at room temperature for 5 min. The yield increased to 58% (Mw / Mn = 1,41) at 50 ºC for 30 min. In the presence of the salt NBu4ClO4, the yield showed no significant changes. It is concluded that the ligands dmso and the studied amines can be selectively used as ancillary ligands in Ru(II) complexes for ROMP reactions inside of an electronic tuning cooperative effect.
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Ferreira, Daniele Marcondes. "Coordenação a centros de rutênio e polimerização via metátese de um novo monômero-ligante do tipo norborneno-piridina." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/75/75135/tde-17042012-170048/.

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O monômero-ligante (3amdpy)2NBE foi sintetizado e caracterizado por análise elementar (CHN), infravermelho e RMN (1H e 13C), tratando-se de um novo ligante quelante que apresenta duas piridinas conectadas ao monômero norborneno via grupos amidas. Esse monômero-ligante foi ligado a um centro de Ru(II)-polipiridínico e o complexo resultante foi caracterizado por análise elementar (CHN), infravermelho, RMN (1H e 13C) e espectrometria de massa como sendo cis-[Ru(bpy)2((3amdpy)2NBE)](PF6)2. O espectro eletrônico do novo complexo apresentou absorção no visível em 460 e 480 nm. Essa bandas são típicas de MLCT com valores de ε na ordem de 104 L cm-1 mol-1. O voltamograma cíclico em CH3CN apresentou um processo redox com potencial de meia-onda de 0,89 V vs Ag/AgCl que é de 60 unidades mais positivo do que o complexo precursor cis- [RuCl2(bpy) 2]. O novo metalo-monômero foi submetido à irradiação a λ= 480 nm, demonstrando ser fotoquimicamente inerte em DMSO, CH3CN, acetona e DMF. A emissão do complexo obtido variou em função do solvente e apresentou maior intensidade de emissão em acetonitrila (λem= 720 nm). A variação do solvente não levou ao deslocamento do máximo de emissão do complexo. O monômero-ligante foi polimerizado via metátese catalisada por catalisador de Grubbs, com 23% de rendimento a 50 °C por 5 min. O polímero foi caracterizado por IV e RMN de 1H. Foi solúvel em água e apresentou um ponto de fusão de 288ºC.
The monomer-ligand (3amdpy)2NBE was synthesized and characterized by elemental analysis (CHN), infrared and NMR (1H and 13C) as a new chelate ligand that features two pyridines connected to the monomer norbornene via amide groups. This monomer-ligand was coordinated to a Ru(II)-polypyridinic center and the resulting complex como sendo cis- [Ru(bpy) 2 ((3amdpy) 2NBE)](PF6)2 was characterized by elemental analysis (CHN), IR, NMR (1H and 13C) and mass spectrometry. The electronic spectrum of the new complex showed absorptions in the visible with bands at 460 and 480 nm. These bands are typical of MLCT with ε values in the order of magnitude of 104 L cm-1 mol-1. The cyclic voltammetry in CH3CN showed a redox process with half-wave potential of 0,89 V vs Ag/AgCl which is ca. 60 units higher than the halfwave potential for the cis-[RuCl2(bpy)2] precursor complex. The new complex was photochemically inert when irradiated at 480 nm either in DMSO, CH3CN, acetone or DMF. The emission of the complex depends on the solvent and presented large emission intensity in acetonitrile (λem = 720 nm). The variation of the solvent does not shift the emission maximum. Ring opening metathesis polymerization of the monomer-ligand (3amdpy)2NBE was carried out at 50 °C for 5 min with 23% of yield using Grubbs type catalyst. The resulting polymer was characterized by IR and NMR-1H. It was water-soluble and showed a melting point of 288°C.
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Henkel, Michael Max Franz Klaus [Verfasser], Thorsten [Akademischer Betreuer] Bach, Thorsten [Gutachter] Bach, and Wolfgang [Gutachter] Eisenreich. "Palladium-katalysierte CH-Aktivierung von Indolen mit 1,n-Dibromiden und chiralen Norbornen-Derivaten / Michael Max Franz Klaus Henkel ; Gutachter: Thorsten Bach, Wolfgang Eisenreich ; Betreuer: Thorsten Bach." München : Universitätsbibliothek der TU München, 2020. http://d-nb.info/1225480035/34.

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Books on the topic "Norbornen"

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Alberico, Dino. Norbornene-mediated palladium-catalyzed synthesis of fused aromatic carbocycles and heterocycles /by Dino Alberico. 2006.

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Eland, John H. D., and Raimund Feifel. Mainly aliphatic molecules. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198788980.003.0007.

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Double photoionisation spectra of homologous iodides and alcohols, acetonitrile, methyl mercaptan, acetaldehyde, acetone, norbornane, cyclooctatetraene, and TMMD are presented. Effects on the spectra of these molecules from electronic state congestion and geometry changes on ionisation mean that only the lowest dication states can be identified. As little detailed analysis of the individual spectra is possible, this chapter presents the molecules in groups rather than individually. In this chapter, molecules are ordered more thematically than strictly by size. The chapter starts with four homologous iodides and three homologous alcohols. Then this chapter takes some individual molecules with different substituent groups and proceed to a few larger molecules. The chapter demonstrates the dominant effect of the distance to which charges can separate in the dication on the double ionisation threshold.
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United States. National Aeronautics and Space Administration., ed. Correlations of norbornenyl crosslinked polymide resin structures with resin thermo-oxidative stability, resin glass transition temperature and composite initial mechanical properties. [Washington, D.C.]: National Aeronautics and Space Administration, 1988.

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Book chapters on the topic "Norbornen"

1

Wohlfarth, Ch. "Second virial coefficient of poly(5-norbornen-2-yl acetate)." In Polymer Solutions, 1018. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_633.

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Sohár, Pál, István Kövesdi, Géza Stájer, and Gábor Bernáth. "Structure Determination of a Norbornane-Norbornene-Fused Pentacyclic Isoxazoline by NMR Spectroscopy." In 25th Congress Ampere on Magnetic Resonance and Related Phenomena, 594. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-76072-3_312.

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Gooch, Jan W. "Norbornene-Spiro-Orthocarbonate." In Encyclopedic Dictionary of Polymers, 489. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7973.

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Yampolskii, Yuri. "Addition Norbornene Polymer-Based Membrane Materials." In Encyclopedia of Membranes, 8. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-44324-8_2149.

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Yampolskii, Yuri. "Metathesis Norbornene Polymer-Based Membrane Materials." In Encyclopedia of Membranes, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-40872-4_2148-1.

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Yampolskii, Yu. "Addition Norbornene Polymer-Based Membrane Materials." In Encyclopedia of Membranes, 1–2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-40872-4_2149-1.

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Schleyer, Paul von R., Vera V. Mainz, and E. Thomas Strom. "Norbornyl Cation Isomers Still Fascinate." In The Foundations of Physical Organic Chemistry: Fifty Years of the James Flack Norris Award, 139–68. Washington, DC: American Chemical Society, 2015. http://dx.doi.org/10.1021/bk-2015-1209.ch007.

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Sevİn, Fatma, and Bülent Düz. "Reactions of Atomic Carbon with 2-Norbornene." In Novel Metathesis Chemistry: Well-Defined Initiator Systems for Specialty Chemical Synthesis, Tailored Polymers and Advanced Material Applications, 303–8. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0066-6_27.

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North, M. "ROMP of Norbornene Derivatives of Peptides and Nucleicacids." In Ring Opening Metathesis Polymerisation and Related Chemistry, 167–76. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0373-5_14.

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Zenkl, Ernst, Michael Schimetta, and Franz Stelzer. "Photoinitiated Thermolysis of Poly(5-norbornene 2,3-dicarboxylates)." In ACS Symposium Series, 370–78. Washington, DC: American Chemical Society, 1993. http://dx.doi.org/10.1021/bk-1994-0537.ch025.

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Conference papers on the topic "Norbornen"

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Bermesheva, Evgeniya, Alyona Wozniak, Gleb Karpov, Alena Zudina, Gleb Chesnokov, Pavel Gribanov, Maxim Topchiy, Andrey F. Asachenko, Mikhail Nechaev, and Maxim Bermeshev. "Addition polymerization of 5-vinyl-2-norbornene and 5-ethylidene-2-norbornene." In 9TH INTERNATIONAL CONFERENCE ON “TIMES OF POLYMERS AND COMPOSITES”: From Aerospace to Nanotechnology. Author(s), 2018. http://dx.doi.org/10.1063/1.5045946.

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Alentiev, Dmitry A., and Maxim V. Bermeshev. "Porous polymers from norbornene derivatives." In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE ON ADVANCED MATERIALS: ICAM 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5130360.

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Silveira, Ingridhy Ostaciana Maia Freitas da, Cristiane Regina Winck, Paola Dias de Oliveira, Roberto da Silva Gomes, Denis Pires de Lima, and Adilson Beatriz. "New Synthesis for norbornene from 4-amoniantipyrine." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20139217404.

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Koh, Meiten, Takuji Ishikawa, Minoru Toriumi, Takayuki Araki, Tsuneo Yamashita, Hirokazu Aoyama, Tamio Yamazaki, Takamitsu Furukawa, and Toshiro Itani. "Synthesis of novel fluorinated norbornene derivatives for 157-nm application." In Microlithography 2003, edited by Theodore H. Fedynyshyn. SPIE, 2003. http://dx.doi.org/10.1117/12.485077.

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Kim, Jin-Baek, Bum-Wook Lee, Jae-Sung Kang, Seong-Ju Kim, Joo Hyeon Park, Dong-Chul Seo, Ki-Ho Baik, Jae Chang Jung, and Chi-Hyeong Roh. "Chemically amplified resists based on the norbornene copolymers with steroid derivatives." In Microlithography '99, edited by Will Conley. SPIE, 1999. http://dx.doi.org/10.1117/12.350194.

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Hagiwara, Takuya, Takamitsu Furukawa, Toshiro Itani, Kiyoshi Fujii, Takuji Ishikawa, Meiten Koh, Tetsuhiro Kodani, et al. "Characterization of TFE/norbornene-based fluoropolymer resist for 157-nm lithography." In Microlithography 2004, edited by John L. Sturtevant. SPIE, 2004. http://dx.doi.org/10.1117/12.535098.

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Sooriyakumaran, Ratnam, Debra Fenzel-Alexander, Phillip J. Brock, Carl E. Larson, Richard A. Di Pietro, Gregory M. Wallraff, Donald C. Hofer, Dan J. Dawson, Arpan P. Mahorowala, and Marie Angelopoulos. "193-nm positive-tone bilayer resist based on norbornene-maleic anhydride copolymers." In Microlithography 2000, edited by Francis M. Houlihan. SPIE, 2000. http://dx.doi.org/10.1117/12.388282.

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Bannaron, Alisa, Andrew Spring, and Shiyoshi Yokoyama. "High-thermal stable poly(norbornene-dicarboximide) for electro-optic polymer modulator (Conference Presentation)." In Organic Photonic Materials and Devices XXII, edited by Christopher E. Tabor, François Kajzar, and Toshikuni Kaino. SPIE, 2020. http://dx.doi.org/10.1117/12.2545453.

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Dai, Bin-Bin, Yue-Xiao Song, Shao-Jie Liu, Zhen Yao, and Kun Cao. "Model Development for Semicontinuous Production of Ethylene and Norbornene Copolymer at Elevated Pressure." In 14th Asia Pacific Confederation of Chemical Engineering Congress. Singapore: Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-07-1445-1_208.

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Huang, Guang Chun, Jong Keun Lee, Michael R. Kessler, and Sungho Yoon. "Adhesion strength of norbornene-based self-healing agents to an amine-cured epoxy." In Second International Conference on Smart Materials and Nanotechnology in Engineering, edited by Jinsong Leng, Anand K. Asundi, and Wolfgang Ecke. SPIE, 2009. http://dx.doi.org/10.1117/12.840356.

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Reports on the topic "Norbornen"

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Mather, Patrick T., Hong G. Jeon, A. Romo-Uribe, Timothy S. Haddad, and Joseph D. Lichtenhan. Mechanical Relaxation and Microstructure of Poly(norbornyl-POSS) Copolymers. Fort Belvoir, VA: Defense Technical Information Center, August 1998. http://dx.doi.org/10.21236/ada409490.

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O'Dell, Richard, David H. McConville, Gretchen E. Hofmeister, and Richard R. Schrock. Polymerization of Enantiomerically Pure 2,3-Dicarboalkoxy Norbornadienes and 5,6-Disubstituted Norbornenes by Well-Characterized Molybdenum ROMP catalysts. Fort Belvoir, VA: Defense Technical Information Center, October 1993. http://dx.doi.org/10.21236/ada272649.

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3

Bazan, G. C., R. R. Schrock, H. N. Cho, and V. C. Gibson. Polymerization of Functionalized Norbornenes Employing Mo(CH-t-Bu)(NAr) (O-t-Bu)2 as the Initiator. Fort Belvoir, VA: Defense Technical Information Center, December 1990. http://dx.doi.org/10.21236/ada230034.

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