Related Experiment Video
Updated: Jan 17, 2026

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Synthesis and ring-opening (co)polymerization of lactones derived from the cotelomerization of isoprene, butadiene,
Ryan J Anderson1, Takuya Akiyama2, Ian A Tonks1
1Department of Chemistry, University of Minnesota-Twin Cities, 207 Pleasant St SE, Minneapolis, Minnesota 55455, USA. itonks@umn.edu.
Abstract:
Herein, we report ring-opening polymerizations and copolymerizations of substituted δ-lactones derived from isoprene, butadiene, and CO2. While the telomerization of CO2 with butadiene to form a disubstituted δ-lactone is well-established, the similar telomerization of isoprene with CO2-or cotelomerization of isoprene and butadiene with CO2-has been less studied. Our initial efforts focused on identifying the factors that govern yield and selectivity in the cotelomerization of isoprene, butadiene, and CO2. The most effective cotelomerization/hydrogenation reaction sequence was scaled-up, leading to mixtures of two isoprene-butadiene coupled lactones, 3-ethyl-6-(prop-1-en-2-yl)tetrahydro-2H-pyran-2-one (EtPeP), and 3-ethyl-6-methyl-6-vinyltetrahydro-2H-pyran-2-one (EtVMeP) and the butadiene homocoupled lactone, 3-ethyl-6-vinyltetrahydro-2H-pyran-2-one (EtVP). The ratios of these three lactones varied depending on the telomerization conditions and purification methods employed. Stepwise syntheses of pure EtVMeP and EtPePvia alternate routes were also carried out. The pure lactones as well as lactone mixtures were subjected to organocatalyzed ring-opening (co)polymerization (ROP) using triazabicyclodecene (TBD), yielding CO2-based copolymers with molar masses (Mn) ranging from 5.5 to 12.7 kDa and narrow dispersities (Đ = 1.3). Increasing the proportion of EtPeP relative to EtVP led to a notable increase in the glass transition temperature (Tg) of the copolymers, reaching -20.5 °C. While EtPeP underwent successful ring-opening polymerization, reactions with EtVMeP resulted in termination of the polymerization owing to the formation of a non-nucleophilic tertiary alkoxide chain end. Thus, small amounts of EtVMeP can have a deleterious effect on copolymerizations of lactone mixtures derived from cotelomerization. These results motivate further development in the selective synthesis of EtPePvia cotelomerization of butadiene and isoprene with CO2.
More Related Videos
05:48Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
11:42Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
Related Concept Videos
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Base-Catalyzed Ring-Opening of Epoxides
Thermal Electrocyclic Reactions: Stereochemistry
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.