Thiol‐Michael coupling and ring‐opening metathesis polymerization: facile access to functional  exo ‐7‐oxanorbornene dendron macromonomers | Zendy

Liu Meina | Zendy; Burford Robert P. | Zendy; Lowe Andrew B. | Zendy

Premium

Thiol‐Michael coupling and ring‐opening metathesis polymerization: facile access to functional exo ‐7‐oxanorbornene dendron macromonomers

Author(s) -

Liu Meina,

Burford Robert P.,

Lowe Andrew B.

Publication year - 2014

Publication title -

polymer international

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.592

H-Index - 105

eISSN - 1097-0126

pISSN - 0959-8103

DOI - 10.1002/pi.4664

Subject(s) - romp , metathesis , polymerization , thioether , monomer , polymer chemistry , dendrimer , nucleophile , ring opening metathesis polymerisation , chemistry , alkoxy group , functional polymers , polymer , organic chemistry , catalysis , alkyl

Thiol‐Michael Coupling and ROMP : Facile Access to Functional exo ‐7‐Oxanorbornene Dendron Macromonomers Nucleophile‐mediated thiol‐Michael coupling is employed to prepare a small library of functional thioether‐based dendron monomers from novel di‐ and tetra‐acrylate functional ring‐opening metathesis polymerization ( ROMP )‐active exo ‐7‐oxanorbornene‐based monomers. The ROMP (co)polymerization of these novel monomers is evaluated with Grubbs 1 st and 3 rd generation initators.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research