Project Details
Description
"Reduction and oxidation are central to chemistry and biology and relate to the addition of electrons or the removal of electrons from substances. Until now, many important but difficult reductions have only been accomplished with very powerful metal reducing agents, like sodium, but we have recently discovered simple neutral organic compounds, composed exclusively of the plentiful elements carbon, hydrogen and nitrogen, that act as powerful reducing agents. In 2012, we found that these substances become even more powerful reducing agents when irradiated with ultra-violet light and are even able to donate electrons to benzene rings that contain no significant electron-withdrawing groups.
We now propose to develop this approach to determine the scope of the chemistry, using visible light to trigger the reactions, rather than ultraviolet light, and converting our transformations it into protocols that use our electron donors catalytically.
We believe that the principal reactions that are currently undertaken by sodium dissolved in liquid ammonia can be undertaken by our reagents in organic solvent and irradiated with light. This will not only add economic benefit through use of catalytic processes, but also convenience and enhancements in safety through avoiding reactive species like sodium that are hazardous both to use and to transport."
We now propose to develop this approach to determine the scope of the chemistry, using visible light to trigger the reactions, rather than ultraviolet light, and converting our transformations it into protocols that use our electron donors catalytically.
We believe that the principal reactions that are currently undertaken by sodium dissolved in liquid ammonia can be undertaken by our reagents in organic solvent and irradiated with light. This will not only add economic benefit through use of catalytic processes, but also convenience and enhancements in safety through avoiding reactive species like sodium that are hazardous both to use and to transport."
Key findings
Organic electron donors are activated through activation by light to achieve reactions that were never witnessed before.
| Status | Finished |
|---|---|
| Effective start/end date | 1/07/13 → 30/06/15 |
Funding
- EPSRC (Engineering and Physical Sciences Research Council): £211,857.00
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Research output
- 12 Article
-
KOtBu: a privileged reagent for electron transfer reactions?
Barham, J. P., Coulthard, G., Emery, K. J., Doni, E., Cumine, F., Nocera, G., John, M. P., Berlouis, L. E. A., McGuire, T., Tuttle, T. & Murphy, J. A., 15 Jun 2016, In: Journal of the American Chemical Society. 138, 23, p. 7402-7410 9 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile288 Link opens in a new tab Citations (Scopus)161 Downloads (Pure) -
Proton transfer reactions of a bridged bis-propyl bis-imidazolium salt
Massey, R. S., Quinn, P., Zhou, S., Murphy, J. A. & O'Donoghue, A. C., 5 May 2016, (E-pub ahead of print) In: Journal of Physical Organic Chemistry. 6 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile10 Link opens in a new tab Citations (Scopus)110 Downloads (Pure) -
Predicting the reducing power of organic super electron donors
Anderson, G. M., Cameron, I., Murphy, J. A. & Tuttle, T., 18 Jan 2016, (E-pub ahead of print) In: RSC Advances. 6, 14, p. 11335-11343 9 p.Research output: Contribution to journal › Article › peer-review
Open AccessFile25 Link opens in a new tab Citations (Scopus)51 Downloads (Pure)