5-di-tert-butyl-4-hydroxyphenoxy)-acetoxy]methyl-5-norbornene (M1) and 3
3
5
5-tetramethyl-4-piperidinyl 5-norbornene-exo
endo-2-carboxylate (M2) were synthesized and polymerized by RuCl2(=CHPh)(PCy3)2 to prepare a novel kind of bi-functional polymer bearing sterically hindered phenol (SHP) and hindered amine (HLAS) groups via ring-opening metathesis polymerization (ROMP). The resulting copolymers were characterized by gel permeation chromatography (GPC)
1H-NMR and differential scanning calorimetry (DSC). The number average molecular weight (Mn) and functional unit content of the resulting copolymer could be regulated by varying the concentration of catalyst and monomer feed.
Abstract
Norbornene derivatives exo
endo-2-[2-(3
5-di-tert-butyl-4-hydroxyphenoxy)-acetoxy]methyl-5-norbornene (M1) and 3
3
5
5-tetramethyl-4-piperidinyl 5-norbornene-exo
endo-2-carboxylate (M2) were synthesized and polymerized by RuCl2(=CHPh)(PCy3)2 to prepare a novel kind of bi-functional polymer bearing sterically hindered phenol (SHP) and hindered amine (HLAS) groups via ring-opening metathesis polymerization (ROMP). The resulting copolymers were characterized by gel permeation chromatography (GPC)
1H-NMR and differential scanning calorimetry (DSC). The number average molecular weight (Mn) and functional unit content of the resulting copolymer could be regulated by varying the concentration of catalyst and monomer feed.
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One-handed Helical Poly(m-terphenyl acetylene)s with Broad Optical Activity Range from Ultraviolet-Visible to Near-infrared Regions
Upgrading Commercially Available Polyethylene to High-value Materials with Strong Mechanical Performance and Hydrophilicity by Blending with Ethylene/meta-Methoxystyrene Copolymers
Highly Regio- and trans-Selective Ring-opening Metathesis Polymerization of Chiral Aza-norbornene with a Simple Phenylimido-Tungsten Catalyst
2026-9 Contents
Porous Organic Polymers for Photocatalytic Hydrogen Peroxide Production: Recent Advances and Future Perspectives