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Synthesis of Conjugated Diblock Copolymers: Two Mechanistically Distinct, Sequential Living Polymerizations using a Single Catalyst

Journal Article · · Polym. Chem.
DOI:https://doi.org/10.1039/C2PY00566B· OSTI ID:1066016
 [1];  [2];  [2];  [2];  [2];  [2]
  1. Hefei Univ. of Technology (China). School of Chemical Engineering
  2. Univ. of Texas, Austin, TX (United States)
Block copolymers comprised of poly(3-hexylthiophene) and three different poly(isocyanide)s were synthesized in a single pot via the sequential addition of 2-bromo-3-hexyl-5-chloromagnesiothiophene followed by 2-(2-methoxyethoxy)ethyl 4-isocyanobenzoate, tert-butyl 4-isocyanobenzoate, or 1-isocyanohexadecane to a solution of 1,3-bis(diphenylphosphino)propane dichloronickel. Similarly, block copolymers of poly(1-dodecylpyrrole) along with poly(2,5-bis(hexyloxy)phenylene) and a poly(arylisocyanide) were also prepared using an analogous methodology. The respective mechanistically distinct polymerizations proceeded in a controlled fashion, were mediated by a common catalyst, and afforded well-defined block copolymers with tunable molecular weights and compositions. Selected block copolymers exhibited higher-order structures in solution and microphase separation characteristics in the solid state.
Research Organization:
Energy Frontier Research Centers (EFRC); Understanding Charge Separation and Transfer at Interfaces in Energy Materials (CST)
Sponsoring Organization:
USDOE
DOE Contract Number:
SC0001091
OSTI ID:
1066016
Journal Information:
Polym. Chem., Journal Name: Polym. Chem. Journal Issue: 4 Vol. 3; ISSN 1759-9954; ISSN PCOHC2
Country of Publication:
United States
Language:
English