4.7 Article

Synthesis of Poly(ionic liquid)s by Atom Transfer Radical Polymerization with ppm of Cu Catalyst

Journal

MACROMOLECULES
Volume 47, Issue 19, Pages 6601-6609

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ma501487u

Keywords

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Funding

  1. NSF [CHE-1039870, DMR-0969301]
  2. DoE [ER-45998]
  3. U.S. Department of Energy's National Energy Technology Laboratory's [DE-FE0004000]
  4. Direct For Mathematical & Physical Scien
  5. Division Of Materials Research [969301] Funding Source: National Science Foundation

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Well-defined poly(ionic liquid)s (PILs) were synthesized by activators regenerated by electron transfer atom transfer radical polymerization (ARGET ATRP). The ionic liquid monomer 1-(4-vinylbenzyl)-3-butylimidazolium bis(trifluoromethylsulfonyl)imide (VBBI(+)Tf2N(-)) was directly polymerized with tris(2-pyridylmethyl)amine (TPMA) ligand and ppm level of copper catalyst. The addition of reducing agent fin(H) 2-ethylhexanoate (Sn-II(EH)(2)) to continuously regenerate the catalyst in the ARGET ATRP enabled the synthesis of PILs with a significantly lower concentration of catalysts than required for a normal ATRP. Pits with well-controlled molecular weight and relatively low dispersity (M-w/M-n < 1.3) were obtained. ATRP chain extension of the resulting Pits with polystyrene revealed that the chain-end functionality of the Pits was significantly improved by slow feeding of the reducing agent during the polymerization. Simple and effective methods were developed to remove the residual halide ions from the ionic liquid monomer by ion exchange with LiTf2N or precipitation with AgTf2N, which allowed ARGET ATRP of the purified ionic liquid monomer to occur with as low as 20 ppm copper catalyst. Additionally, ARGET ATRP was used for the preparation of Pit block copolymers, including AB diblock and ABA triblock with PM segment(s) as the middle or side blocks, using ionic liquid monomer or mono/difunctional PIL macroinitiators.

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