Suppressing carboxylate nucleophilicity with inorganic salts enables selective electrocarboxylation without sacrificial anodes. Issue 37 (20th August 2021)
- Record Type:
- Journal Article
- Title:
- Suppressing carboxylate nucleophilicity with inorganic salts enables selective electrocarboxylation without sacrificial anodes. Issue 37 (20th August 2021)
- Main Title:
- Suppressing carboxylate nucleophilicity with inorganic salts enables selective electrocarboxylation without sacrificial anodes
- Authors:
- Corbin, Nathan
Yang, Deng-Tao
Lazouski, Nikifar
Steinberg, Katherine
Manthiram, Karthish - Abstract:
- Abstract : Selective electrocarboxylation of nucleophilically susceptible organic halides without sacrificial anodes is enabled by inorganic salt additives, which suppress the nucleophilicity of anions in the electrolyte. Abstract : Although electrocarboxylation reactions use CO2 as a renewable synthon and can incorporate renewable electricity as a driving force, the overall sustainability and practicality of this process is limited by the use of sacrificial anodes such as magnesium and aluminum. Replacing these anodes for the carboxylation of organic halides is not trivial because the cations produced from their oxidation inhibit a variety of undesired nucleophilic reactions that form esters, carbonates, and alcohols. Herein, a strategy to maintain selectivity without a sacrificial anode is developed by adding a salt with an inorganic cation that blocks nucleophilic reactions. Using anhydrous MgBr2 as a low-cost, soluble source of Mg 2+ cations, carboxylation of a variety of aliphatic, benzylic, and aromatic halides was achieved with moderate to good (34–78%) yields without a sacrificial anode. Moreover, the yields from the sacrificial-anode-free process were often comparable or better than those from a traditional sacrificial-anode process. Examining a wide variety of substrates shows a correlation between known nucleophilic susceptibilities of carbon–halide bonds and selectivity loss in the absence of a Mg 2+ source. The carboxylate anion product was also discovered toAbstract : Selective electrocarboxylation of nucleophilically susceptible organic halides without sacrificial anodes is enabled by inorganic salt additives, which suppress the nucleophilicity of anions in the electrolyte. Abstract : Although electrocarboxylation reactions use CO2 as a renewable synthon and can incorporate renewable electricity as a driving force, the overall sustainability and practicality of this process is limited by the use of sacrificial anodes such as magnesium and aluminum. Replacing these anodes for the carboxylation of organic halides is not trivial because the cations produced from their oxidation inhibit a variety of undesired nucleophilic reactions that form esters, carbonates, and alcohols. Herein, a strategy to maintain selectivity without a sacrificial anode is developed by adding a salt with an inorganic cation that blocks nucleophilic reactions. Using anhydrous MgBr2 as a low-cost, soluble source of Mg 2+ cations, carboxylation of a variety of aliphatic, benzylic, and aromatic halides was achieved with moderate to good (34–78%) yields without a sacrificial anode. Moreover, the yields from the sacrificial-anode-free process were often comparable or better than those from a traditional sacrificial-anode process. Examining a wide variety of substrates shows a correlation between known nucleophilic susceptibilities of carbon–halide bonds and selectivity loss in the absence of a Mg 2+ source. The carboxylate anion product was also discovered to mitigate cathodic passivation by insoluble carbonates produced as byproducts from concomitant CO2 reduction to CO, although this protection can eventually become insufficient when sacrificial anodes are used. These results are a key step toward sustainable and practical carboxylation by providing an electrolyte design guideline to obviate the need for sacrificial anodes. … (more)
- Is Part Of:
- Chemical science. Volume 12:Issue 37(2021)
- Journal:
- Chemical science
- Issue:
- Volume 12:Issue 37(2021)
- Issue Display:
- Volume 12, Issue 37 (2021)
- Year:
- 2021
- Volume:
- 12
- Issue:
- 37
- Issue Sort Value:
- 2021-0012-0037-0000
- Page Start:
- 12365
- Page End:
- 12376
- Publication Date:
- 2021-08-20
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1sc02413b ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 19631.xml