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Synthesis of Norbornenyl Telechelic Polyphosphazenes and Ring-Opening Metathesis Polymerization Reactions

✍ Scribed by Allcock, Harry R.; de Denus, Christine R.; Prange, Robbyn; Laredo, Walter R.


Book ID
121337071
Publisher
American Chemical Society
Year
2001
Tongue
English
Weight
195 KB
Volume
34
Category
Article
ISSN
0024-9297

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πŸ“œ SIMILAR VOLUMES


Synthesis of Ξ±-norbornenyl polystyrene m
✍ ValΓ©rie Heroguez; Yves Gnanou; Michel Fontanille πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 295 KB

## Abstract Polystyrene macromonomers, fitted with a norbornenyl unsaturation in Ξ± position, have been obtained from a norbornene based carbanionic initiator that has been purposely designed to this end. The advantages of this synthetic scheme over that based on the deactivation of living PS chains

Synthesis of Ξ±- and Ο‰-norbornenyl-polybu
✍ ValΓ©rie HΓ©roguez; Jean-Luc Six; Yves Gnanou; Michel Fontanille πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 626 KB

Norbornene-ended polybutadiene (PBu) macromonomers have been prepared via two different routes: a-norbornenyl-polybutadiene was derived from a norbornene-containing carbanionic initiator, whereas w-norbornenyl samples were obtained through deactivation of living polybutadienyl anions by a norbornene

Ring-opening metathesis polymerization o
✍ D. Mecerreyes; D. Dahan; Ph. Lecomte; Ph. Dubois; A. Demonceau; A. F. Noels; R. πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 216 KB πŸ‘ 1 views

Poly(-caprolactone) (PCL) macromonomers capped by a polymerizable norbornene end-group have been synthesized and (co)polymerized by ring-opening metathesis with formation of graft copolymers and polymacromonomers. ␣-Norbornenyl PCL macromonomers have been synthesized by ring opening polymerization (