Binary Alkoxide Ionic Liquids

Peter McNeice; Andrew C. Marr; Patricia C. Marr; Martyn J. Earle; Kenneth R. Seddon

doi:10.1021/acssuschemeng.8b04299

Binary Alkoxide Ionic Liquids

Peter McNeice, Andrew C. Marr, Patricia C. Marr, Martyn J. Earle, Kenneth R. Seddon

School of Chemistry and Chemical Engineering

Research output: Contribution to journal › Article › peer-review

9 Citations (Scopus)

227 Downloads (Pure)

Abstract

Strongly basic, stable ionic liquids are rare. We report the synthesis of a series of stable binary alkoxide ionic liquids. The Hammett Basicity of these ionic liquids is comparable to or greater than traditional bases such as pyridine and NaOMe. The ionic liquids catalyse the Knoevenagel condensation of malononitrile and benzaldehyde, with the best system displaying higher activity than pyridine and NaOMe; and the Aldol condensation of acetone and benzaldehyde.

Original language	English
Pages (from-to)	13676–13680
Number of pages	5
Journal	ACS Sustainable Chemistry & Engineering
Volume	6
Issue number	11
Early online date	25 Sep 2018
DOIs	https://doi.org/10.1021/acssuschemeng.8b04299
Publication status	Published - 25 Sep 2018

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Binary Alkoxide Ionic Liquids
© 2018 American Chemical Society. This work is made available online in accordance with the publisher’s policies. Please refer to any applicable terms of use of the publisher.
Accepted author manuscript, 225 KBLicence: Unspecified

Base stable and basic ionic liquids for catalysis
Author: McNeice, P., Jul 2020
Supervisor: Marr, A. (Supervisor), Seddon, K. (Supervisor) & Marr, P. (Supervisor)
Student thesis: Doctoral Thesis › Doctor of Philosophy

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Andrew Marr
- a.marrqub.acuk
- School of Chemistry and Chemical Engineering - Senior Lecturer
- Organic Synthesis and Chemical Biology
Person: Academic

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title = "Binary Alkoxide Ionic Liquids",

abstract = "Strongly basic, stable ionic liquids are rare. We report the synthesis of a series of stable binary alkoxide ionic liquids. The Hammett Basicity of these ionic liquids is comparable to or greater than traditional bases such as pyridine and NaOMe. The ionic liquids catalyse the Knoevenagel condensation of malononitrile and benzaldehyde, with the best system displaying higher activity than pyridine and NaOMe; and the Aldol condensation of acetone and benzaldehyde.",

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AU - McNeice, Peter

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AU - Marr, Patricia C.

AU - Earle, Martyn J.

AU - Seddon, Kenneth R.

PY - 2018/9/25

Y1 - 2018/9/25

N2 - Strongly basic, stable ionic liquids are rare. We report the synthesis of a series of stable binary alkoxide ionic liquids. The Hammett Basicity of these ionic liquids is comparable to or greater than traditional bases such as pyridine and NaOMe. The ionic liquids catalyse the Knoevenagel condensation of malononitrile and benzaldehyde, with the best system displaying higher activity than pyridine and NaOMe; and the Aldol condensation of acetone and benzaldehyde.

AB - Strongly basic, stable ionic liquids are rare. We report the synthesis of a series of stable binary alkoxide ionic liquids. The Hammett Basicity of these ionic liquids is comparable to or greater than traditional bases such as pyridine and NaOMe. The ionic liquids catalyse the Knoevenagel condensation of malononitrile and benzaldehyde, with the best system displaying higher activity than pyridine and NaOMe; and the Aldol condensation of acetone and benzaldehyde.

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DO - 10.1021/acssuschemeng.8b04299

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EP - 13680

JO - ACS Sustainable Chemistry & Engineering

JF - ACS Sustainable Chemistry & Engineering

SN - 2168-0485

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Binary Alkoxide Ionic Liquids

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Student Theses

Base stable and basic ionic liquids for catalysis

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Andrew Marr

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