Relative Reactivity of Dicyclopentadiene and 2,3-Dicarbomethoxy-5-norbornene in Metathesis Copolymerization and the Properties of the Copolymer

[1]  F. Verpoort,et al.  Novel Polymers Based on Dimethyl Esters of Norbornene Dicarboxylic Acids Synthesized Using Metathesis Ring-Opening Polymerization , 2017 .

[2]  A. Lyapkov,et al.  Polymers Based on Norbornene Derivatives , 2015 .

[3]  H. Nishide,et al.  Synthesis of Pendant Radical- and Ion-Containing Block Copolymers via Ring-Opening Metathesis Polymerization for Organic Resistive Memory. , 2014, ACS macro letters.

[4]  S. Kiselev,et al.  The relative reactivity of 2,3‐dicarbomethoxy‐5‐norbornenes in metathesis polymerization using the original n‐chelating ruthenium carbene complex , 2014 .

[5]  M. Bermeshev,et al.  Solubility controlled permeation of hydrocarbons: New membrane materials and results , 2014 .

[6]  S. Kiselev,et al.  Kinetics of the metathesis polymerization of 5,6-Di(methoxycarbonyl)bicyclo[2.2.1]hept-2-enes on an original Hoveyda-Grubbs II type catalyst , 2013, Kinetics and Catalysis.

[7]  Yiwang Chen,et al.  Nickel(II) Complexes with Three-Dimensional Geometry α-Diimine Ligands: Synthesis and Catalytic Activity toward Copolymerization of Norbornene , 2013 .

[8]  M. Pitsikalis,et al.  Ring Opening Metathesis Polymerization of Norbornene and Derivatives by the Triply Bonded Ditungsten Complex Na[W2(µ-Cl)3Cl4(THF)2]·(THF)3 , 2012 .

[9]  R. Schrock,et al.  Five-Coordinate Rearrangements of Metallacyclobutane Intermediates during Ring-Opening Metathesis Polymerization of 2,3-Dicarboalkoxynorbornenes by Molybdenum and Tungsten Monoalkoxide Pyrrolide Initiators , 2012 .

[10]  K. Ogino,et al.  Stereo-Selective Synthesis of 5-Norbornene-2-exo-carboxylic Acid—Rapid Isomerization and Kinetically Selective Hydrolysis , 2012 .

[11]  A. Greiner,et al.  Synthesis and characterization of substituted polynorbornene derivatives , 2011 .

[12]  C. Slugovc,et al.  Pyridine as trigger for chloride isomerisation in chelated ruthenium benzylidene complexes: implications for olefin metathesis. , 2011, Chemical communications.

[13]  W. Binder,et al.  Synthesis and crossover reaction of TEMPO containing block copolymer via ROMP , 2010, Beilstein journal of organic chemistry.

[14]  F. Verpoort,et al.  Ruthenium-based olefin metathesis catalysts derived from alkynes. , 2010, Chemical reviews.

[15]  Y. Nishihara,et al.  Enantioseparation of doubly functionalized polar norbornenes by HPLC and their ruthenium-catalyzed ring-opening metathesis polymerization , 2010 .

[16]  Jonathan Clayden,et al.  Looking forward to volume six , 2010, Beilstein journal of organic chemistry.

[17]  V. Dragojlovic,et al.  Solvent-free Diels–Alder reactions of in situ generated cyclopentadiene , 2009 .

[18]  R. Grubbs,et al.  Living ring-opening metathesis polymerization , 2007 .

[19]  Y. Nishihara,et al.  Comparative reactivity of exo- and endo-isomers in the ru-initiated ring-opening metathesis polymerization of doubly functionalized norbornenes with both cyano and ester groups , 2006 .

[20]  A. Kenwright,et al.  Nature of the Propagating Species in Ring-Opening Metathesis Polymerizations of Oxygen-Containing Monomers Using Well-Defined Ruthenium Initiators , 2005 .

[21]  R. Schrock.  High oxidation state alkylidene and alkylidyne complexes. , 2005, Chemical communications.

[22]  A. Kenwright,et al.  Ring opening metathesis polymerisations of norbornene and norbornadiene derivatives containing oxygen: a study on the regeneration of Grubbs catalyst , 2004 .

[23]  Johannes C. Mol,et al.  Industrial applications of olefin metathesis , 2004 .

[24]  C. Slugovc,et al.  The Resting State Makes the Difference: The Influence of the Anchor Group in the ROMP of Norbornene Derivatives , 2004 .

[25]  F. Verpoort,et al.  Easily accessible and robust olefin-metathesis catalysts based on ruthenium vinylidene complexes , 2003 .

[26]  M. Weck,et al.  Living ROMP of exo-Norbornene Esters Possessing PdII SCS Pincer Complexes or Diaminopyridines , 2003 .

[27]  R. Schrock.  High oxidation state multiple metal-carbon bonds. , 2002, Chemical reviews.

[28]  K. J. Ivin,et al.  Ring‐Opening Metathesis Polymerization of 7‐tert‐Butoxybicyclo[2.2.1]hepta‐2,5‐diene Initiated by Well‐Defined Molybdenum and Ruthenium Carbene Complexes , 2001 .

[29]  M. Kerr,et al.  Highly selective Diels-Alder reactions of dienophiles with 1, 3-cyclohexadiene mediated by Yb(OTf)(3).2H(2)O and ultrahigh pressures. , 2000, Organic letters.

[30]  M. Buchmeiser.  Homogeneous Metathesis Polymerization by Well-Defined Group VI and Group VIII Transition-Metal Alkylidenes: Fundamentals and Applications in the Preparation of Advanced Materials. , 2000, Chemical reviews.

[31]  M. Piotti.  Ring opening metathesis polymerization , 1999 .

[32]  O. Nuyken,et al.  N-Heterocyclic carbenes: application of ruthenium–alkylidene complexes in ring-opening metathesis polymerization , 1999 .

[33]  F. Lefebvre,et al.  Effect of alcohols and epoxides on the rate of ROMP of norbornene by a ruthenium trichloride catalyst , 1998 .

[34]  K. J. Ivin,et al.  Olefin metathesis and metathesis polymerization , 1997 .

[35]  J. Wendorff,et al.  Polynorbornene: synthesis, properties and simulations , 1996 .

[36]  Joice P. Mathew,et al.  (η3-Allyl)palladium(II) and Palladium(II) Nitrile Catalysts for the Addition Polymerization of Norbornene Derivatives with Functional Groups , 1996 .

[37]  R. Grubbs,et al.  Synthesis of block copolymers of silicon-containing norbornene derivatives via living ring-opening metathesis polymerization catalyzed by a ruthenium carbene complex , 1995 .

[38]  B. Goodall,et al.  New catalysts for the polymerization of cyclic olefins , 1995 .

[39]  R. Schrock,et al.  Polymerization of Enantiomerically Pure 2,3-Dicarboalkoxynorbornadienes and 5,6-Disubstituted Norbornenes by Well-Characterized Molybdenum Ring-Opening Metathesis Polymerization Initiators. Direct Determination of Tacticity in Cis, Highly Tactic and Trans, Highly Tactic Polymers , 1994 .

[40]  W. Risse,et al.  Transition‐metal‐catalyzed vinyl addition polymerizations of norbornene derivatives with ester groups , 1992 .

[41]  A. Gol'berg,et al.  Ring‐opening metathesis polymerization of norbornenes with organosilicon substituents. Gas permeability of polymers obtained , 1991 .

[42]  K. J. Ivin,et al.  Metathesis polymerization of substituted norbornenes: microstructure of the polymers of some ester derivatives , 1989 .

[43]  Y. Yamashita,et al.  Polynorbornenes with Oligodimethylsiloxanyl Substituents for Selectively Oxygen Permeable Membrane Material , 1988 .

[44]  S. Frenkel',et al.  Topological Principles of the Analysis of Binary Statistical Copolymerisation , 1978 .

[45]  B. Turcsányi,et al.  Analysis of Linear Methods for Determining Copolymerization Reactivity Ratios. III. Linear Graphic Method for Evaluating Data Obtained at High Conversion Levels , 1976 .

[46]  B. Mandal,et al.  Peroxide‐induced polymerization of norbornene , 1976 .

[47]  T. Kelen.  Analysis of the Linear Methods for Determining Copolymerization Reactivity Ratios. I. A New Improved Linear Graphic Method , 1975 .

[48]  A. I. Yezrielev,et al.  An analytical method for calculating reactivity ratios , 1969 .

[49]  R. Hoffmann.  Orbital Symmetries and endo-exo Relationships in Concerted Cycloaddition Reaction (福井謙一とフロンティア軌導理論) -- (参考論文) , 1965 .

[50]  R. M. Joshi,et al.  A modified method of deriving the reactivity constants r1 and r2 in copolymerization , 1954 .

[51]  S. Ross,et al.  Linear method for determining monomer reactivity ratios in copolymerization , 1950 .

[52]  F. Mayo,et al.  Copolymerization. I. A Basis for Comparing the Behavior of Monomers in Copolymerization; The Copolymerization of Styrene and Methyl Methacrylate , 1944 .