ISSN:
0887-624X
Keywords:
acyclic dience metathesis
;
ADMET
;
depolymerization
;
aqueous ring-opening metathesis polymerization
;
ROMP
;
Chemistry
;
Polymer and Materials Science
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
Notes:
Acyclic dience metathesis (ADMET) depolymerization of functionalized furan-based polymers prepared via aqueous ring-opening polymerization of 7-oxanobornenes has been investigated. Results indicate that while very high molecular weight poly [exo-N-methyl-7-oxabicyclo [2.2.1] hept-2,5-diene-2,3-dicarboximide] can be depolymerized to oligomers with ease, poly [2,3-dicarbomethoxy-7-oxabicyclo [2.2.1] hept-2,5-diene] is more resistant to depolymerization under similar conditions. This difference may be due to differential interaction of the carbonyls in the side chains with the metal atom of the catalyst in the proposed metallacyclobutane intermediate. ADMET depolymerization of poly [2,3-bis (trifluoromethyl)-7-oxabicyclo [2.2.1] hept-2,5-diene] was feasible, however, the extent of depolymerization was decreased due to the use of a coordinating solvent (THF) used during the depolymerization process. © 1994 John Wiley & Sons, Inc.
Additional Material:
7 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/pola.1994.080321308
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