Determination of the tacticities of ring-opened metathesis polymers of symmetrical 5,6-disubstituted derivatives of norbornene and norbornadiene from the 13C NMR spectra of their hydrogenated derivatives
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,Process Chemistry and Technology,Catalysis
Reference12 articles.
1. K.J. Ivin, J.C. Mol, Olefin Metathesis and Metathesis Polymerization, Academic Press, London, 1997.
2. Synthesis of chiral molybdenum ROMP initiators and all-cis highly tactic poly(2,3-(R)2norbornadiene) (R = CF3 or CO2Me)
3. 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
4. Tactiticy and stereochemistry in the ring-opening polymerization of 5,5-dimethylbicyclo[2.2.1]hept-2-ene initiated by metathesis catalysts
5. Ring-Opening Metathesis Polymerization of (+)- and (.+-.)-endo,exo-5,6-Dimethylbicyclo[2.2.1]hept-2-ene by Mo(CH-t-Bu)(N-2,6-C6H3-i-Pr2)(OR)2
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3. Investigation of Tacticity and Living Characteristics of Photoredox‐Mediated Metal‐Free Ring‐Opening Metathesis Polymerization;Macromolecular Rapid Communications;2017-02-13
4. Chain Elongation Influence in Copolymerization with Different Diesters of Norbornene 2,3-Dicarboxylic Acid Monomers via ROMP under Air Atmosphere;Journal of the Brazilian Chemical Society;2017
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