2008Polymers for Advanced TechnologiesRequires access

Anionic polymerization of methyl methacrylate in an ionic liquid

Hisashi Kokubo, Masayoshi Watanabe

Open publisher page 39 citations

Abstract

Abstract Anionic polymerization reactions of methyl methacrylate (MMA) in ionic liquids were carried out by utilizing alkyl lithium initiators such as n‐butyl lithium (n‐BuLi) and diphenylhexyl lithium (DPHLi). The polymerization in ionic liquids having bis(trifluoromethyl sulfonyl)amide ([NTf2]) anion did not yield poly(MMA) (PMMA), because of the deactivation of the initiator due to an attack on the trifluoromethyl group. By using 1‐butyl‐3‐methylimidazolium hexafluorophosphate ([C4mim][PF6]), the polymerization reactions proceeded. The PMMA prepared in [C4mim][PF6] gave low yields (5–9%), as compared with those (15–62%) obtained for PMMA prepared in tetrahydrofuran (THF), and the prepared PMMA had large polydispersity indices (≅2.0). The results obtained can be attributed to the high reaction temperature (0°C), in comparison to the common anionic polymerization temperature of MMA, −78°C, and the reaction between the initiator and the imidazolium cation. The initiator was considered to be deactivated because the hydrogen atom at the 2‐position of the imidazolium ring was withdrawn by the alkyl lithium initiator. The tacticity of the obtained PMMA, prepared in [C4mim][PF6] by utilizing DPHLi, was rich in mm triads, similar to that polymerized in toluene. Copyright © 2008 John Wiley & Sons, Ltd.

About this research paper

What this paper is about

Abstract Anionic polymerization reactions of methyl methacrylate (MMA) in ionic liquids were carried out by utilizing alkyl lithium initiators such as n‐butyl lithium (n‐BuLi) and diphenylhexyl lithium (DPHLi). The polymerization in ionic liquids having bis(trifluoromethyl sulfonyl)amide ([NTf2]) anion did not yield poly(MMA) (PMMA), because of the deactivation of the initiator due to an attack on the trifluoromethyl group. By using 1‐butyl‐3‐methylimidazolium hexafluorophosphate ([C4mim][PF6]), the polymerization reactions proceeded. The PMMA prepared in [C4mim][PF6] gave low yields (5–9%), as compared with those (15–62%) obtained for PMMA prepared in tetrahydrofuran (THF), and the prepared PMMA had large polydispersity indices (≅2.0). The results obtained can be attributed to the high reaction temperature (0°C), in comparison to the common anionic polymerization temperature of MMA, −78°C, and the reaction between the initiator and the imidazolium cation. The initiator was considered to be deactivated because the hydrogen atom at the 2‐position of the imidazolium ring was withdrawn by the alkyl lithium initiator. The tacticity of the obtained PMMA, prepared in [C4mim][PF6] by utilizing DPHLi, was rich in mm triads, similar to that polymerized in toluene. Copyright © 2008 John Wiley & Sons, Ltd.

Why it matters

OpenAlex reports 39 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract Anionic polymerization reactions of methyl methacrylate (MMA) in ionic liquids were carried out by utilizing alkyl lithium initiators such as n‐butyl lithium (n‐BuLi) and diphenylhexyl lithium (DPHLi). The polymerization in ionic liquids having bis(trifluoromethyl sulfonyl)amide ([NTf2]) anion did not yield poly(MMA) (PMMA), because of the deactivation of the initiator due to an attack on the trifluoromethyl group. By using 1‐butyl‐3‐methylimidazolium hexafluorophosphate ([C4mim][PF6]), the polymerization reactions proceeded. The PMMA prepared in [C4mim][PF6] gave low yields (5–9%), as compared with those (15–62%) obtained for PMMA prepared in tetrahydrofuran (THF), and the prepared PMMA had large polydispersity indices (≅2.0). The results obtained can be attributed to the high reaction temperature (0°C), in comparison to the common anionic polymerization temperature of MMA, −78°C, and the reaction between the initiator and the imidazolium cation. The initiator was considered to be deactivated because the hydrogen atom at the 2‐position of the imidazolium ring was withdrawn by the alkyl lithium initiator. The tacticity of the obtained PMMA, prepared in [C4mim][PF6] by utilizing DPHLi, was rich in mm triads, similar to that polymerized in toluene. Copyright © 2008 John Wiley & Sons, Ltd.

Key concepts: Polymerization, Polymer chemistry, Ionic liquid, Anionic addition polymerization, Methyl methacrylate, Tetrahydrofuran, Materials science, Alkyl

Related papers

Back to paper searchBrowse research topicsOriginal source
Anionic polymerization of methyl methacrylate in an ionic liquid — Research Paper | ScholarLens