The effect of the hydroxyl group position on the electrochemical reactivity and product selectivity of butanediol electro-oxidation

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The effect of the hydroxyl group position on the electrochemical reactivity and product selectivity of butanediol electro-oxidation
Title:
The effect of the hydroxyl group position on the electrochemical reactivity and product selectivity of butanediol electro-oxidation
Journal Title:
Dalton Transactions
Publication Date:
02 September 2022
Citation:
Sun, S., Dai, C., Sun, L., Seh, Z. W., Sun, Y., Fisher, A., Wang, X., & Xu, Z. J. (2022). The effect of the hydroxyl group position on the electrochemical reactivity and product selectivity of butanediol electro-oxidation. Dalton Transactions, 51(38), 14491–14497. https://doi.org/10.1039/d2dt02450k
Abstract:
In the electro-oxidation of butanediols, closer hydroxyl groups lead to higher electrochemical reactivities. Vicinal hydroxyl groups facilitate the formation of a carboxylate group, and the following C–C bond cleavage.
License type:
Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
Funding Info:
This research / project is supported by the Ministry of Education - Tier 2
Grant Reference no. : MOE-T2EP10220-0001

This research / project is supported by the National Research Foundation - Campus for Research Excellence and Technological Enterprise (CREATE) programme
Grant Reference no. : NA

This research / project is supported by the National Research Foundation - NRF Fellowship
Grant Reference no. : NRF-NRFF2017-04

This research / project is supported by the Nanyang Technological University - Centre of Advanced Catalysis Science and Technology
Grant Reference no. : NA

This research is supported by core funding from: SERC
Grant Reference no. : Central Research Fund Award
Description:
ISSN:
1477-9234
1477-9226
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