Microfluidic electrochemistry for single-electron transfer redox-neutral reactions

Author:

Mo Yiming1ORCID,Lu Zhaohong2ORCID,Rughoobur Girish3ORCID,Patil Prashant4ORCID,Gershenfeld Neil4ORCID,Akinwande Akintunde I.3,Buchwald Stephen L.2ORCID,Jensen Klavs F.1ORCID

Affiliation:

1. Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

2. Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

3. Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

4. Center for Bits and Atoms, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Abstract

Cutting it close for radical coupling In principle, electrochemistry is an ideal method for radical coupling: One precursor oxidized at the anode pairs up with a counterpart that has been reduced at the cathode. The trouble is that either or both coupling partners might not stay stable long enough to meet in the middle. Mo et al. resolved this issue by closely spacing the electrodes in a microfluidics platform (see the Perspective by Liu et al. ). They showcase coupling of dicyanobenzene as the cathodic radical precursor with a variety of oxidatively generated partners. Science , this issue p. 1352 ; see also p. 1312

Funder

Novartis-MIT Center for Continuous Manufacturing

Chyn Duog Shiah Memorial Fellowship

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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