4.8 Article

Electrochemical β-Selective Hydrocarboxylation of Styrene Using CO2 and Water

Journal

ADVANCED SCIENCE
Volume 7, Issue 3, Pages -

Publisher

WILEY
DOI: 10.1002/advs.201900137

Keywords

carbon fixation; carboxylation; CO2 reduction; electrochemistry

Funding

  1. KIST Institutional Program [2V06170]
  2. National Research Foundation of Korea (NRF) - Korea government (MIST) [NRF-2017R1A2B3012003]
  3. Creative Materials Discovery Program through the NRF - Ministry of Science and ICT [NRF-2017M3D1A1039377]
  4. Global Frontier R&D Program of the Center for Multiscale Energy System - NRF under the Ministry of Science and ICT, Korea [2012M3A6A7054855]
  5. Korea CCS R&D Center (Korea CCS 2020 Project) - Korea government (Ministry of Science, ICT & Future Planning) [NRF-2016M1A8A1925427]
  6. National Research Foundation of Korea [2017R1A2B3012003, 2E30300] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The carboxylation of hydrocarbons using CO2 as a one-carbon building block is an attractive route for the synthesis of carboxylic acids and their derivatives. Until now, chemical carboxylation catalyzed by organometallic nucleophiles and reductants has been generally adopted particularly for the precise selectivity control of carboxylation sites. As another approach, electrochemical carboxylation has been attempted but these carboxylation reactions are limited to only a few pathways. In the case of styrene, dicarboxylation at the alpha- and beta-positions is mostly observed with electrochemical carboxylation while site-selective hydrocarboxylations are hardly achieved. In this study, electrochemical beta-selective hydrocarboxylation of styrene using CO2 and water is developed, in which the site selectivity can be precisely controlled between beta-hydrocarboxylation and dicarboxylation without the aid of homogeneous catalysts. In this platform, water is used as proton source in the beta-hydrocarboxylation of styrene where its addition results in significant enhancement of the selectivity toward beta-hydrocarboxylation. This work provides insights into new strategies for site-selectivity-controllable carboxylation with CO2 using an electrochemical platform.

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