4.4 Article

Metal-free terpolymerization of propylene oxide, carbon dioxide, and carbonyl sulfide: A facile route to sulfur-containing polycarbonates with gradient sequences

Journal

JOURNAL OF POLYMER SCIENCE
Volume 60, Issue 24, Pages 3414-3419

Publisher

WILEY
DOI: 10.1002/pol.20220166

Keywords

carbon dioxide; carbonyl sulfide; metal-free catalysis; propylene oxide; sulfur-containing polycarbonates

Funding

  1. Zhejiang Provincial Department of Science and Technology [2020R52006]
  2. National Science Foundation of the People's Republic of China [51973190]

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This study presents a facile method to improve the optical properties of polycarbonate by introducing sulfur atoms into its chains. The one-pot/one-step synthesis of sulfur-containing polycarbonate was achieved using propylene oxide, carbon dioxide, and carbonyl sulfide, with the catalytic effect of a metal-free Lewis acid-base pair. The obtained terpolymers exhibit high molecular weight, narrow dispersity, and adjustable gradient sequence of thiocarbonate units by varying the feed ratio of carbonyl sulfide.
Introducing sulfur atoms into polycarbonate can improve its optical properties, but is limited by the lack of efficient synthetic methods. Here we develop a facile method to achieve the one-pot/one-step incorporation of sulfur atoms into polycarbonate chains using raw chemicals of propylene oxide (PO), carbon dioxide (CO2), and carbonyl sulfide (COS). The metal-free Lewis acid-base pair composed of N, N-dimethylcyclohexylamine combined with triethyl borane can effectively catalyze the terpolymerization of PO, CO2, and COS, affording a sulfur-containing polycarbonate with high molecular weight (M-n) up to 58.4 kDa and narrow dispersity (D = 1.24-1.56). The obtained terpolymers display gradient sequence with tunable thiocarbonate units (27%-81%) upon simply varying the feed ratio of COS. The refractive indices of the terpolymers can be enhanced up to 1.55 at high thiocarbonate content, suggesting promising applications of the terpolymer in optical materials.

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