Low Polydispersity Homo- and Block Copolymers by Ring-Opening of 5,6-Dicarbomethoxynorbornene.

Abstract

Addition of 50-200 eq of norbornene to Mo(CH Superscript t Bu) (NAr) (O Superscript t Bu)2 yields living polymers, Mo?CH(C5H8)CHxCH Superscript t Bu (NAr)(O Superscript t Bu)2 (55% trans), that are stable for days in the absence of water and oxygen with essentially no isomerization of the double bonds in the chain. Addition of benzaldehyde cleaves off the polymer in a Wittig-like reaction to yield polynorbornenens with polydispersities in the range 1.04-1.11. Analogous reactions involving 50-200 eq of endo, endo-5,6-dicarbomethoxynorbornene yields homopolymers with polydispersities in the range 1.11-1.22. Block copolymers containing 50 eq of endo,endo-5,6-dicarbomethoxynorbornene and 200 eq of norbornene prepared by adding one or the other monomer first are virtually identical (polydispersities 1.06 and 1.09 with M sub n 57200 and 59900, respectively). These results suggest that the molybdenum catalyst will not react significantly with up to 100 eq of ester functionality during the time of a typical polymerization reaction (approx. 15 m at 25 degs.).

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Document Details

Document Type
Technical Report
Publication Date
Jul 31, 1987
Accession Number
ADA183245

Entities

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  • John S. Murdzek
  • Richard R. Schrock

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  • Massachusetts Institute of Technology

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