TY - JOUR
T1 - Storable, Dual-Component Systems for Frontal Ring-Opening Metathesis Polymerization
AU - Suslick, Benjamin A.
AU - Yazdani, Aliza N.
AU - Cencer, Morgan M.
AU - Paul, Justine E.
AU - Parikh, Nil A.
AU - Stawiasz, Katherine J.
AU - Qamar, Isabel P.S.
AU - Sottos, Nancy R.
AU - Moore, Jeffrey S.
N1 - Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/7/12
Y1 - 2022/7/12
N2 - Frontal ring-opening metathesis polymerization (FROMP) catalyzed by Grubbs-type Ru complexes enables new, rapid, and energy-efficient syntheses of high-performance, structural plastics. Ideal catalysts survive the extended time periods associated with resin preparation, storage, and transportation. Current catalysts, however, induce premature polymerization within hours to days under ambient conditions. In this work, a thermally latent bis-N-heterocyclic carbene complex provides exceedingly robust resins, which are viable for 8 weeks. When mixed with CuIcoreagents, precatalyst activation primes the system for rapid reactivity after thermal initiation. In this study, more than 40 dual-component formulations successfully catalyzed FROMP of dicyclopentadiene. The polymerization process parameters (front temperatures and velocities), resin storability, and resultant polymer properties (e.g., Tg) were determined for each composition. Intriguingly, the Cu to Ru ratio dramatically impacts the observed frontal velocity and temperature, as well as the polymer glass-transition temperature; slower, colder reaction fronts result from formulations with large Cu to Ru ratios. The resultant polymers display lower Tgvalues. Mechanistic analysis of a related model system demonstrated that an excess Cu reagent decreases the activation and polymerization rates.
AB - Frontal ring-opening metathesis polymerization (FROMP) catalyzed by Grubbs-type Ru complexes enables new, rapid, and energy-efficient syntheses of high-performance, structural plastics. Ideal catalysts survive the extended time periods associated with resin preparation, storage, and transportation. Current catalysts, however, induce premature polymerization within hours to days under ambient conditions. In this work, a thermally latent bis-N-heterocyclic carbene complex provides exceedingly robust resins, which are viable for 8 weeks. When mixed with CuIcoreagents, precatalyst activation primes the system for rapid reactivity after thermal initiation. In this study, more than 40 dual-component formulations successfully catalyzed FROMP of dicyclopentadiene. The polymerization process parameters (front temperatures and velocities), resin storability, and resultant polymer properties (e.g., Tg) were determined for each composition. Intriguingly, the Cu to Ru ratio dramatically impacts the observed frontal velocity and temperature, as well as the polymer glass-transition temperature; slower, colder reaction fronts result from formulations with large Cu to Ru ratios. The resultant polymers display lower Tgvalues. Mechanistic analysis of a related model system demonstrated that an excess Cu reagent decreases the activation and polymerization rates.
UR - http://www.scopus.com/inward/record.url?scp=85134009379&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85134009379&partnerID=8YFLogxK
U2 - 10.1021/acs.macromol.2c00775
DO - 10.1021/acs.macromol.2c00775
M3 - Article
AN - SCOPUS:85134009379
SN - 0024-9297
VL - 55
SP - 5459
EP - 5473
JO - Macromolecules
JF - Macromolecules
IS - 13
ER -