Title: PolyDODT: a macrocyclic elastomer with unusual properties

Journal Article · · Polymer Chemistry
DOI: https://doi.org/10.1039/d1py01426a · OSTI ID:1846575
ORCiD logo [1];  [2];  [3]; ORCiD logo [4];  [4];  [5];  [2]; ORCiD logo [6]; ORCiD logo [4]
  1. The Ohio State Univ., Wooster, OH (United States); North Carolina State University
  2. California Institute of Technology (CalTech), Pasadena, CA (United States)
  3. Texas Tech Univ., Lubbock, TX (United States)
  4. The Ohio State Univ., Wooster, OH (United States)
  5. Texas Tech Univ., Lubbock, TX (United States); North Carolina State Univ., Raleigh, NC (United States)
  6. The Ohio State Univ., Columbus, OH (United States)

The effect of reaction conditions on the structure of poly(3,6-dioxa-1,8-octanedithiol) (polyDODT) made by Reversible Radical Recombination Polymerization (R3P) using triethylamine (TEA), H2O2 and air was investigated. 800 MHz (1 and 2D) NMR was used to investigate the polymer structures. Sensitivity analysis provided direct evidence for high purity cyclic polyDODT up to Mn ~ 100 000 g mol–1. Here, comparative analysis by High Resolution Multidetector Size Exclusion Chromatography (SEC) using integrated data showed that the cycles had lower viscosity and were more compact (both for Rg and Rh) than linear samples of similar molecular weight. However, differential data revealed unusual behavior. While lower molecular weight cyclic polymers eluted later and had lower intrinsic viscosity than their linear counterparts at the same molecular weight, at higher molecular weights the polymers showed strange behavior: both the diffusion coefficient measured by Quasielastic Light Scattering (QELS) and Mark–Houwink–Sakurada plots of intrinsic viscosity for linear and cyclic polyDODT were found to converge. R3P, an aqueous based “green” method is capable of producing polymers at the 10–100 g scale in the lab, which will allow more detailed studies of this new class of biodegradable elastomers so further experimentation can be performed to elucidate the reasons for the unusual findings.

Research Organization:
California Institute of Technology (CalTech), Pasadena, CA (United States); Texas Tech Univ., Lubbock, TX (United States); The Ohio State Univ., Columbus, OH (United States)
Sponsoring Organization:
USDOE; USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
SC0018655; SC0018657; SC0018891
OSTI ID:
1846575
Journal Information:
Polymer Chemistry, Journal Name: Polymer Chemistry Journal Issue: 5 Vol. 13; ISSN 1759-9954
Publisher:
Royal Society of ChemistryCopyright Statement
Country of Publication:
United States
Language:
English

References (28)

Cyclic polymers: Methods and strategies journal February 2012
Synthesis and characterization of ring polybutadienes journal June 1988
Liquid chromatography at critical conditions (LCCC): Capabilities and limitations for polymer analysis journal January 2021
Cyclic Poly(4-methyl-1-pentene): Efficient Catalytic Synthesis of a Transparent Cyclic Polymer journal September 2020
Melt Rheology of Ring Polystyrenes with Ultrahigh Purity journal April 2015
When Ends Meet: Circular DNA Stretches Differently in Elongational Flows journal August 2015
Synthesis of Biodegradable Polyisobutylene Disulfides by Living Reversible Recombination Radical Polymerization (R3P): Macrocycles? journal March 2017
Intrinsic Viscosity of Cyclic Polystyrene journal September 2017
Green Polymer Chemistry: Living Dithiol Polymerization via Cyclic Intermediates journal December 2011
Synthesis of Cyclic Polybutadiene via Ring-Opening Metathesis Polymerization:  The Importance of Removing Trace Linear Contaminants
  • Bielawski, Christopher W.; Benitez, Diego; Grubbs, Robert H.
  • Journal of the American Chemical Society, Vol. 125, Issue 28, p. 8424-8425 https://doi.org/10.1021/ja034524l
journal July 2003
End Group Characterization of Poly(phthalaldehyde): Surprising Discovery of a Reversible, Cationic Macrocyclization Mechanism journal August 2013
Monte Carlo calculation of hydrodynamic properties of linear and cyclic polymers in good solvents journal January 1991
Fractionation of Cyclic Polystyrene from Linear Precursor by HPLC at the Chromatographic Critical Condition journal October 2000
Radii of Gyration of Ring-Shaped Polystyrenes with High Purity in Dilute Solutions. journal December 2011
Cyclic polymers from alkynes journal May 2016
Unexpected power-law stress relaxation of entangled ring polymers journal October 2008
Universal size ratios of Gaussian polymers with complex architecture: radius of gyration vs hydrodynamic radius journal August 2020
Topological polymer chemistry: a cyclic approach toward novel polymer properties and functions journal January 2011
Viscosity, Sedimentation, et Cetera, of Ring‐ and Straight‐Chain Polymers in Dilute Solution journal January 1966
Hydrodynamic Properties of Flexible‐Ring Macromolecules journal June 1966
Diffusion of isolated DNA molecules: Dependence on length and topology journal April 2006
Unexpected Stretching of Entangled Ring Macromolecules journal May 2019
An "Endless" Route to Cyclic Polymers journal September 2002
Preparation and Characterization of Cyclic Polystyrenes journal July 2005
Green polymer chemistry: Living oxidative polymerization of dithiols journal May 2012
Enhancement of Microbial Biodesulfurization via Genetic Engineering and Adaptive Evolution journal January 2017
Green Polymer Chemistry: Investigating the Mechanism of Radical Ring-Opening Redox Polymerization (R3P) of 3,6-Dioxa-1,8-octanedithiol (DODT) journal April 2015
Synthesis of High Performance Cyclic Olefin Polymers (COPs) with Ester Group via Ring-Opening Metathesis Polymerization journal August 2015